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TP53 (Tumour protein p53 (Li-Fraumeni syndrome))

Written1998-07Richard Hamelin, Jean-Loup Huret
INSERM U434, Laboratoire de Genetique des Tumeurs, CEPH, Paris (RH),, Genetics, Dept Medical Information, University of Poitiers; CHU Poitiers Hospital, F-86021 Poitiers (JLH), France.
Updated1998-10Richard Hamelin, Jean-Loup Huret
INSERM U434, Laboratoire de Genetique des Tumeurs, CEPH, Paris (RH),, Genetics, Dept Medical Information, University of Poitiers; CHU Poitiers Hospital, F-86021 Poitiers (JLH), France.
Updated2001-12Thierry Soussi
Laboratoire de Genotoxicologie des tumeurs, Institut Curie, Universite Pierre et Marie Curie, 26 rue d'Ulm, 75005 Paris, France.
Updated2002-10Thierry Soussi
Laboratoire de Genotoxicologie des tumeurs, Institut Curie, Universite Pierre et Marie Curie, 26 rue d'Ulm, 75005 Paris, France.
Updated2007-04Magali Olivier
Molecular Carcinogenesis, Biomarkers Group, International Agency for Research on Cancer (IARC/CIRC), 150 Cours Albert Thomas, F-69372 Lyon CEDEX 08, France
Updated2016-04Thierry Soussi
Sorbonne Université, UPMC Univ Paris 06, F- 75005 Paris, France; INSERM, U1138, Centre de Recherche des Cordeliers, Paris, France; Department of Oncology-Pathology, Karolinska Institutet, Cancer Center Karolinska (CCK) R8:04, Stockholm SE-171 76, Sweden. thierry.soussi@ki.se

Abstract Review on CTCF, with data on DNA, on the protein encoded, and where the gene is implicated.

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Identity

Other namesBCC7
LFS1
P53
TRP53
HGNC (Hugo) TP53
LocusID (NCBI) 7157
Atlas_Id 88
Location 17p13.1
Location_base_pair Starts at 7571720 and ends at 7590868 bp from pter ( according to hg19-Feb_2009)  [Mapping]
 
  Probe(s) - Courtesy Mariano Rocchi, Resources for Molecular Cytogenetics
Fusion genes
(updated 2016)
MPRIP (17p11.2) / TP53 (17p13.1)RBBP8 (18q11.2) / TP53 (17p13.1)TP53 (17p13.1) / C17orf39 ()
TP53 (17p13.1) / FARP2 (2q37.3)TP53 (17p13.1) / GID4 (17p11.2)TP53 (17p13.1) / NTRK1 (1q23.1)

DNA/RNA

 
  Diagram of the TP53 gene. Exons are represented by boxes with numbers and sizes inside. Intron sizes (not drawn to scale) are also indicated. Translated exons for the canonical TP53 protein (393 aa) are shown in light green, in red for isoforms beta and in blue for isoforms gamma.
 
Description The TP53 gene spans a region of 32,772 bp. The protypical TP53 gene is composed of 11 exons. Two novel alternatively spliced exons localized in intron 9 have been identified (exons 9β and 9γ).
To solve some confusing situation on TP53 nomenclature, an international consortium has joined forces with the Locus Reference Genomic (LRG) consortium to provide a stable reference sequence and a coordinate system for permanent and unambiguous reporting of disease-causing variants in genes related to any pathology. The TP53 nomenclature can be reached at http://ftp.ebi.ac.uk/pub/databases/lrgex/LRG_321.xml.
Transcription The transcription of the TP53 is highly complex and can vary between tissue and/or cellular context. Different p53 mRNA variants are expressed through the use of alternative splicing and an internal promoter in intron 4.

Protein

 
  Diagram of TP53α, the major TP53 protein expressed in normal cells. TAD1: transactivation domain 1; TAD2: transactivation domain 2; Pro: proline- rich domain; DBD: DNA binding domain; NES: nuclear exclusion signal: NLS: nuclear localization signal; Oli: oligomerization domain; C-ter: carboxy-terminus domain. I to V correspond to the five highly conserved domains of the protein.
Description At least, 12 TP53 isoforms are expressed but the full-length protein (TP53 p1 or TP53α is always the major species detected in every tissue.
The p1 protein contains from N-term to C-term, two transactivationg domains (TAD1, 1-40 and TAD2, 41-61), a proline rich domain (63-97), a specific DNA binding domain (102-292), 3 nuclear localization signals (305-322), a tetramerization domain that includes a nuclear export signal (325-355) and a negative regulatory domain (360-393).
Shorter C-terminal TP53 isoforms do not contain either the tetramerization domain or the negative regulatory domain.
Shorter N-terminal TP53 isoforms do not contain TAD1 (Δ40 TP53 isoforms), TAD1, TAD2 and the proline rich domain (Δ133) or TAD1, TAD2, the proline rich domain and part of the DNA binding domain (Δ160)
TP53 is modified by numerous post-translational modifications phosphorylation, acetylation, ubiquitination, sumoylation, neddylation, methylation, ADP ribosylation, and glycosylation. Acetylation of multiple residues is essential for TP53 activation and DNA transcriptional activity.
 
  Domains in the various TP53 isoforms. TAD1: transactivation domain 1; TAD2: transactivation domain 2; Pro: proline- rich domain; NES: nuclear exclusion signal: NLS: nuclear localization signal; Oli: oligomerization do- main; C-ter: carboxy-terminus domain.
The LRG nomenclature used for TP53 protein (p1 to p13) and RNA (t1 to t8) is also shown on the right.
Expression Widely expressed.
 
  Pathway i) the stress signals activate the pathway; ii) the upstream mediators detect and interpret the upstream signals; iii) the core regulation of TP53 is disrupted leading to TP53 accumulation and activation; iv) the downstream events, mainly transcriptional activation or protein-protein interaction v) The final outcome.
Localisation Nucleus
Function The transcription factor TP53 is at the centre of a network that integrates and transmits multiple signals generated during various stress events to ensure cell and tissue homeostasis. This network also includes the two other members of the TP53 family, TP63 and TP73 as well as the two negative regulators, MDM2 and MDM4 (MDMX).
The p53 response can be conveniently divided into two sets of pathways acting upstream and downstream the core regulation of TP53.
The upstream pathways (stress signal detection and integration)
Multiple type of stress such as DNA damage, hypoxia, nucleotides pool depletion, viral infection, oncogene activation or oxidative stress can elicit a TP53 response. For each stress, a different panel of mediators is recruited.
In most cases, the goal of this step is the disruption of the TP53-MDM2 interaction leading to an accumulation and an activation of the TP53 protein. Subsequent post translational modifications (phosphorylation and acetylation principally) modulate TP53 activity depending of the type and the intensity of the damage and the cellular context.
For DNA damage, the ATM and CHEK2 kinase will phosphorylate TP53, MDM2 and MDM4 to release the negative regulation of the regulatory proteins.
For ribosomal stress, free ribosomal proteins will bind and sequester MDM2, relieving its inhibitory
For oncogene activation (hyperproliferative stress), the P16-ARF protein will sequester MDM2 in the nucleolus and relieve its inhibitory activity.
The core regulation of TP53
In normal tissues, TP53 protein levels are maintained at a very low level predominantly by the action of specific E3 ligases such as MDM2 and the ubiquitin proteosome pathway. Other E3 ligases such as Pirrh2, RFWD2 or TRIM24 target TP53 and able to regulate its stability.
TP53 translation is also highly regulated and enhanced after various types of stress. TP53 mRNA includes two Internal Ribosome Entry Sites (IRESs) elements. The first IRES is located in the 5'UTR of the full-length isoform, the second is located into the protein-coding region and mediates the translation of a ΔN-p53 isoform.
The downstream pathways (effectors activation and TP53 response)
Several thousand genes have been shown to be activated by TP53 upon various types of stress. Different sets of genes are associated with a specific response. Initially, apoptosis, growth arrest and senescence have been considered to be the main response to TP53 activation. More recent studies have emphasized the importance of TP53 in other cellular responses such as DNA repair, metabolism and regulation of the Warburg effect, autophagy and regulation of stemm cell maintenance.
Although growth arrest, apoptosis and senescence were originally associated with the tumour suppressor activity of TP53, their importance has recently been challenged. Several mouse models defective for these three T53 activities lack any predisposition to develop neoplasia.
TP53 also has cytoplasmic transcription-independent functions (apoptosis and autophagy) via a direct interaction with pro- and anti-apoptotic factors in mitochondria.
ResponseGene
ApoptosisAPAF1 ; BAX - FAS - - MIR34A - PMAIP1 ; TP53AIP1 - PERP -PIDD1 - TP53I3 - BBC3 - SIVA1 ; TNFS10
Growth arrestYWHAZ ; BTG2 ; CDKN1A - GADD45A ; MIR34A ; MIR34B / MIR34C ; Prl13; PTPRVP ; RPRM
SenescenceCDKN1A ; SERPINE1 ; PML
DNA repairDbd2; ERCC5 ; FANCC ; GADD45A ; XRCC5 ; MGMT ; MLH1 ; MSH2 ; RRM2B ; PAPD7 ; XPC
Metabolism / Anti oxydantADORA2B ; ALDH4A1 ; PRKAB1 ; GAMT ; GLS2 ; SLC2A1 (-);SLC2A4  (-);GPX1 ; IGFBP3 ; LPIN1 ; PARK2 ; VCAN (-); PRKAB1 ID:44100 ; PRKAB2 ; ten; SCO1 ; SESN1 ; SESN2 ; TIGAR ; TP53INP1 ;
AutophagyATG10 ; ATG2B ; ATG4A ; ATG4C ; ATG7 ; CTSD ; DDIT4 ; DRAM1 ; RBFOX3 ; LAPTM4A ; STK11 ; PIK3R3 ; PRKAG2 ; BBC3 ; ACD ; TSC2 ; ULK1 ; ULK2 ; UVRAG ; VAMP4 ; VMP1
Tumour micro environmentADGRB1 ; CX3CL1 ; ICAM1 ; IRF9 ; ISG15 ; SERPINB5 ; CCL2 ; NCF2 ; SERPINE1 ; TLR1 - TLR10 ; PRSS55 ; ULBP1 ; ULBP2
Invasion metastasisCDKN1A ; MIR34A ; MIR200C
Stem cell biologyCDKN1A ; MIR145 ; MIR34A ; MIR34B / MIR34C ; NOTCH1
TP53 regulationCARD16 ; MDM2 , PIRH-2; TP63 , TP73
Unknown*APOBEC3H; HRAS ; TNFAIP8 ; ZMAT3

This list is not exhaustive. Several TP53 responses overlap and include identical genes. Adapted from Bieging et al. with modifications.
* Genes induced by TP53 without any clear relation to a specific pathway

Mutations

 
  Accumulation of mutant TP53 if tumoural cells
 
 
Germinal Germline TP53 mutations are associated with Li-Fraumeni (LFS) and Li-Fraumeni-like syndromes (LFL), characterized by a familial clustering of tumours, with a predominance of soft tissue and bone sarcomas, breast cancers, brain tumours, and adrenocortical carcinomas, diagnosed before the age of 45 years. TP53 germline mutations have also been observed in families at high risk of breast cancer, albeit at very low frequency.
A founder mutation TP53 (NG_017013.2:g.21852G>A, p.R337H) is detected in 0.3% of the general population in southern Brazil. This mutation is associated with an increased risk of childhood adrenal cortical carcinoma (ACC) but is also common in Brazilian LFS/LFL families.
The frequency of TP53 de novo germline mutation ranges between 7 and 20%.
Somatic Mutation of the TP53 gene can be found in 50% of human cancer. More than 80% of TP53 mutations are missense mutations that lead to the synthesis of a stable oncogenic protein that accumulates in the nucleus of tumour cells. The frequency of TP53 alterations range from less than 5% in cervical carcinoma to 90% in ovarian carcinoma or Small Cell Lung Cancer (SCLC) but these numbers must be taken with caution due to several factors such as the subtype of the cancer (lung or breast cancer), the stage of the tumour (prostate carcinoma or chronic lymphocytic leukaemia) and exogenous features such as viral or bacterial infection.
Two international consortiums have reported the sequencing of more than 10.000 tumour genomes and confirmed that the TP53 gene is the most frequently mutated gene in human cancer. TP53 mutations are strongly associated with tumours with high chromosomal instability.
Cancer specific driver genes can be noticed: APC in colorectal carcinoma (violet); VHL in kidney cancer (green) or PTEN and PIK3CA in endometrial carcinoma (green and red)
Molecular epidemiology studies demonstrate a link between exposure to various types of carcinogens, specific mutational events in the TP53 gene and the development of specific cancers.
Lung cancer
TP53 mutations in lung cancer are mostly GC to TA transversions, with a rate of transition mutations lower than in other cancers. There is a strong correlation between the frequency of these GC to TA transversions and lifetime cigarette smoking. This high frequency of GC to TA transversions has not been detected for other cancers such as colon, breast, ovary or brain cancer, which are not directly associated with smoking. This observation is compatible with the role of exogenous carcinogens such as benzo(a)pyrene in lung cancer. After metabolic activation, one of the derivative products of benzo(a)pyrene, the prime carcinogen in cigarette smoke, binds predominantly to guanine and gives rise to specific G-C to T-A transversions. Exposure of cells to benzo(a)pyrene lead to the formation of adducts at codon 157, 248 and 273 in the p53 gene. These positions are the major mutational hotspots in human lung cancer but not in other cancers. The p53 gene is one of the targets of carcinogens found in tobacco.
Liver cancer
There is a strong association between infection with hepatitis B virus and hepatocellular carcinoma. Aflatoxin B1 has been considered to be a significant etiological factor for liver cancer in Western Africa and Asia. Aflatoxins are compounds produced by fungal strains (such as Aspergillus flavus for aflatoxins B1) that are known food contaminants in these countries. Aflatoxins are highly carcinogenic in experimental animals, producing liver tumours in newborn mice, rats, fish, ducks and monkeys.
Worldwide epidemiological studies showed that a specific mutation at codon 249 (c.747G>T, p.R249S) is specifically found in liver cancer from countries in which food was contaminated by aflatoxin B1. In countries which do not consume contaminated food (including Europe and the USA), TP53 mutations are scattered along the central part of p53, as for the other types of cancer. In vitro and in vivo analysis showed a specific binding of aflatoxin B1 to codon 249 of the TP53 gene.
Bladder cancer
Aristolochic acid (AA), a common ingredient in many Chinese herbs, is a powerful nephrotoxin and human carcinogen associated with chronic kidney disease and upper urinary tract urothelial carcinomas including bladder cancer. AA exposure is also associated with Balkan endemic nephropathy (BEN) similarly characterized by kidney failure and a high frequency of transitional cancer of urothelial tracts including bladder, renal pelvis and ureters.
TP53 mutation from patients exposed to AA display a high frequency A:T-to-T:A transversions, a mutational signature associated with AA which forms a covalent adduct with adenine that leads to this transversion.
Skin cancer
Ultraviolet (UV) light induces specific DNA damage such as cyclobutane pyrimidine dimers (CPDs) and pyrimidine(6-4)pyrimidine photoproducts (64PPs) at dipyrimidine sites, where two pyrimidine (Py) bases are juxtaposed in tandem in the nucleotide sequence of DNA. If left unrepaired, this lesion leads to specific types of mutation: base substitutions of cytosine (C) → thymine (T) at dipyrimidine sites and CC → TT tandem base substitutions. These two types of mutation are called UV signature and their detection suggests past exposure to UV. In skin cancer such as squamous cell carcinoma (SCC) and basal cell carcinoma (BCC), the frequency of TP53 is high (70 to 80%) with more than 15% of tandem mutations (less than 1% for other cancer types).
Colorectal or brain cancer
The cytosine-guanine (CpG) dinucleotide is a hotspot for pathological mutations in the human genome. This hypermutability is due to its role as the major site of cytosine methylation with the attendant risk of spontaneous deamination of 5-methylcytosine (5mC) to yield C → T and G → A transitions. Most TP53 hotspots for mutations in colorectal or brain cancer are located at CpG sites with a mutation spectrum compatible with 5-methylcytosine deamination. These hotspot codons, CGN at positions 175, 248 or 273, encode arginine residues important for TP53 structure and/or activity. It is interesting to note that arginine can also be encoded by AGG and AGA that have the same frequency of usage in human but are not targeted by methylation. It has not yet been determined whether or not there is a specific selection to keep CGN in the TP53.

Implicated in

Entity Skin cancers (non melanoma)
Disease Non melanoma skin cancers are the most common form of cancer, globally accounting for at least 40% of human cancer. About 80% are basal-cell cancers (BCC) and 20% squamous-cell cancers (SCC). Most skin cancer cases are caused by exposure to ultraviolet radiation from the sun.
Prognosis Patients with primary cutaneous SCC or BCC have a very good prognosis.
Oncogenesis The hedgehog signalling pathway (HH pathway) is the primary target in BCC with mutations in PTCH1, SMO or SFU. TP53 mutations are found in 60% of BCC. In SCC, the frequency of TP53 mutation varies between 40 to 80% depending on the aggressivity of the tumour or the seuqnecing methodology. Deep sequencing allows the detection of multiple subclones with different TP53 mutations.
The pattern of TP53 mutations in skin cancer is highly related to UV exposure.
  
Entity Skin cancers (Melanoma)
Disease Case per year (thousands) 132; death per year (thousands) 31. Melanoma is a skin tumours characterized by the malignant growth of melanocytes. The incidence is continuing to increase worldwide and UV exposure is a known risk factor for melanoma. Epidemiologic data suggest that gender and genetics may influence the distribution of melanoma on the body surface and histopathologic characteristics of the lesion.
Oncogenesis The MAPK pathway is the primary target in melanoma with mutations in BRAF1 (50%) or NRAS (20%). TP53 gene mutations are rare in melanoma (5%) but the apoptotic function of the protein is often impaired. Melanoma often loses , a cell-death effector that acts with cytochrome c and CASP9 to mediate p53-dependent apoptosis. It may contribute to the low frequency of TP53 mutations observed in this highly chemoresistant tumour type. Alteration of CDKN2A in 30% of melanoma could also contribute to TP53 deficiency.
  
Entity Lung cancers
Disease Case per year (thousands) 1,825; death per year (thousands) 1,590 (Worldwide ranks, cases / deaths: 1/1). There are 2 main types of lung cancer: about 10% to 15% are small cell lung cancer (SCLC) and 85% to 90% arenon-small cell lung cancer (NSCLC). There are several subtypes of NSCLC, Adenocarcinoma (50%), Squamous cell carcinoma (30%); Large cell carcinoma (15%) and other (includes carcinoid and neurodendocrine tumours) (5%).
 
Frequency of TP53 mutation in various subtypes of lung carcinoma
Oncogenesis In SCLC, recent studies using Novel Generation Sequencing showed that TP53 mutations can be found in 95% of the cases. In NSCLC, the frequency of TP53 mutations varies among the subtypes. The frequency of TP53 mutations is the highest in squamous cell carcinomas (70 to 80%) and lower in adenocarcinomas (50%). Lung cancer from smokers shows a distinct, unique TP53 mutation spectrum with G to T transversions at codons 157, 158, 179, 248, and 273, which is uncommonly observed in lung cancer from non-smokers or in cancer unrelated to tobacco smoking such as colorectal or brain tumours.
  
Entity Breast cancer
Disease Case per year (thousands) 1,677; death per year (thousands) 522 (Worldwide ranks, cases / deaths: 2/5). Breast carcinoma is a heterogeneous disease with multiple subtypes defined either histologically or more recently via gene expression.
 
Frequency of TP53 mutation in various subtypes of breast carcinoma
Oncogenesis In Triple Negative Breast Cancer (TNBC, 10-15% of breast cancer with low or lack of expression of estrogen (ER) and progesterone (PR) receptors, lack of human epidermal growth factor receptor 2 (HER2 ) over-expression and a worse prognostic), the frequency of TP53 is high (80%).
Molecular profiling studies have identified four major subtypes of breast cancer: luminal A, luminal B, basal like, and HER2. The frequency of TP53 alteration in these subtypes ranges from 12% in luminal A, 30% in luminal B, 70% in HER2 to more than 80% in basal like. There is a partial overlap between TNBC and Basal like.
  
Entity Colorectal cancers
Disease Case per year (thousands) 1,360; death per year (thousands) 693 (Worldwide ranks, cases / deaths: 3/4). CRC is a heterogeneous disease classically divided into three sub-types
(i) Chromosomal instability (CIN) characterized by microsatellite stable tumours (MSS), loss of heterozygosity and major chromosomal changes in tumour-suppressor genes and oncogenes (60% of CRC)
(ii) The CpG island methylator phenotype (CIMP) which causes transcriptional silencing by methylation of CpG-rich regions in the promoter of tumour-suppressor genes (10 to 15% of CRC).
(iii) Microsatellite instability (MSI) is characterized by the accumulation of frame shift mutations in microsatellite sequences due to a deficiency in mismatch repair (MMR) genes (10 to 15% of CRC)
Cytogenetics MSI tumour are generally characterized by diploid or near-diploid cells
 
TP53 mutations are not frequent (20%) in MSI low diploid or in CIMP tumours but can reach 50 to 60% in MSS aneuploid tumours.
Oncogenesis The most frequently mutated genes in CRC are KRAS, APC and TP53.
  
Entity Prostate cancer
Disease cases per year (thousands): 1,112; deaths per year (thousands): 307 (Worldwide ranks, cases / deaths: 4/8). Prostate carcinoma is characterized by a high genetic and clinical heterogeneity with multiple subclones.
 
The frequency of TP53 mutation in localized prostate cancer is low but deep sequencing can pick up rare TP53 mutations that will be selected during the progression of the disease. The frequency of TP53 mutation can reach 40 to 50% during metastasis development.
Oncogenesis TP53 mutations are infrequent in primary disease and are mostly found in patients with metastatic disease
  
Entity Gastric cancer
Disease cases per year (thousands): 952 ; deaths per year (thousands): 723 (Worldwide ranks, cases / deaths: 5/3). Risk factors for gastric cancer include: Helicobacter pylori gastric infection, advanced age, male gender, diet including dry salted foods, atrophic gastritis, pernicious anemia, cigarette smoking, Menetrier's disease , and familial polyposis. Adenocarcinoma histology accounts for 90% to 95% of all gastric malignancies. The prognosis of patients with gastric cancer is related to tumour extent and includes both nodal involvement and direct tumour extension beyond the gastric wall. Tumour grade may also provide some prognostic information.
Oncogenesis TP53 is the most frequently mutated gene in gastric carcinoma with a frequency ranging between 40 and 60%.
  
Entity
Disease cases per year (thousands): 782 ; deaths per year (thousands): 746 (Worldwide ranks, cases / deaths: 6/2). Most patients with HCC (70 to 90%) have an established background of chronic liver disease and cirrhosis, with major risk factors for developing cirrhosis including chronic infection with hepatitis B virus (HBV), hepatitis C virus (HCV), Alcoholism, and nonalcoholic steatohepatitis (NASH). Additional risk factors include intake of aflatoxin-B1 contaminated food (China and West Africa), diabetes, obesity, certain hereditary conditions such as hemochromatosis, and some metabolic disorders.
Cytogenetics Losses of 1p, 4q, 5p, 5q, 8q, 13q, 16p, 16q, and 17p in 20 to 50% of cases.
Oncogenesis Somatic mutations in the TERT (coding for telomerase reverse transcriptase) promoter is the most frequent genetic alteration in hepatocellular carcinoma (HCC). These mutations created a potential binding site for ETS transcription factors and are predicted to increase promoter activity and TERT transcription. Mutated genes in HCC are TP53, beta-catenin (CTNNB1 ) and ARIDA1. TP53 mutations are more frequent in patients associated with HBV infection compared to those associated with alcoholism. The frequency and the pattern of TP53 mutations in HCC show a high geographical variation depending on HBV infection prevalence or aflatoxin consumption. In areas of high aflatoxin exposure, 50% of HCC cases bear a specific AGG to AGT point mutation in codon 249 of the p53 tumour suppressor gene. A second mutation at codon 157 is also frequent albeit at lower frequency. Exposure of cells to aflatoxin B1 leads to the formation of adducts at codon 249 in the p53 gene.
  
Entity Cervical cancer
Disease Cases per year (thousands): 527 ; deaths per year (thousands): 265 (Worldwide ranks, cases / deaths: 7/10). Almost all cervical cancers are caused by HPV (human papilloma virus). There are more than 100 types of HPV, of which at least 13 are cancer-causing (also known as high-risk type) including HPV16 and 18.
Oncogenesis The UBE3A (E6) oncoprotein produced by the high-risk type of HPV stimulates ubiquitinylation and proteasome-dependent degradation of the tumour suppressor p53 via the formation of a trimeric complex comprising E6, p53, and E6-AP. TP53 mutation is therefore very infrequent in cervical cancer.
  
Entity Oesophagus cancers
Disease Case per year (thousands) 455; death per year (thousands) 400 (worldwide ranks 8/6) There are two main types of esophageal carcinoma, squamous cell carcinoma and adenocarcinoma. Most adenocarcinomas arise in Barrett esophagus that develops in response to chronic gastroesophageal reflux.
Oncogenesis The frequency of TP53 mutation is high in both types, ADC and SCC, and can reach 70%. TP53 mutations are an early event in ADC as it can be found in Barrett esophagus.
  
Entity Bladder cancer
Disease Case per year (thousands) 429; death per year (thousands) 165 (worldwide ranks 9/12).
Prognosis Highly variable, according to the stage and the grade.
Cytogenetics -9, -11 or del(11p), del(17p) and LOH at 17p, del(13q), frequent other LOH, aneuploidy, polyploidy, complex karyotypes.
Oncogenesis TP53 mutation are found in 40 to 50% of bladder carcinoma. Three variants are particularly frequent in bladder cancer: c.853G>A; p.E285K, c.839G>C; p.R280T and c.839G>A; p.R280K.
  
Entity Pancreatic cancer
Disease Case per year (thousands) 338; death per year (thousands) 330 (worldwide ranks 12/7); Pancreatic cancers are divided into two major subtypes: adenocarcinoma (95% of cases), and rare endocrine tumours often designated as neuroendocrine tumours.
Prognosis Pancreatic cancer is one of the most deadly of all types of cancer.
Oncogenesis KRAS mutation is the most frequent genetic variation in pancreatic adenocarcinoma (95%) followed by TP53 mutation (60-70%) and CDKN2A deletion (50%).
  
Entity Head and neck squamous cell carcinoma
Disease Head and neck cancer encompasses malignant tumours arising within the upper aerodigestive tract. The major etiologic agents are tobacco and alcohol consumption and for some cases human papilloma virus (HPV) infection. More than 90% of head and neck cancers are squamous cell carcinomas, which originate from the mucosal surfaces of the lip and oral cavity, nasopharynx, oropharynx, hypopharynx, and larynx.
Oncogenesis TP53 mutation can be found in about 60 to 70% of HPV positive HNSCC cancers. The frequency is lower in HPV negative tumours (less than 10%)
  
Entity Ovary carcinoma
Disease Case per year (thousands) 238; death per year (thousands) 152 (worldwide ranks 18/13). Based on histopathology, immunohistochemistry, and molecular genetic analysis, at least five main types of ovarian carcinomas are identified: high-grade serous carcinomas (HGSCs; 70%), endometrioid carcinomas (EC; 10%), clear-cell carcinomas (CCC; 10%), mucinous carcinomas (MC; 3%), and LGSC (<5%). These tumours account for 98% of ovarian carcinomas.
 
Frequency of TP53 mutation in ovarian carcinoma
Oncogenesis In HGSC, the frequency of TP53 mutation reaches 95% and is the most frequent genetic alteration in this subtype.
  
Entity sarcoma
Disease Osteosarcoma is a primary bone malignancy with a particularly high incidence rate in children and adolescents relative to other age groups.
 
OncoPrint of genetic alterations for TP53 and MDM2 in sarcoma. The OncoPrint view provides an overview of genomic alterations in particular genes (horizontal rows) affecting particular individual samples in a large cohort (vertical columns). For each patient, alteration in a specific set of genes is immediately identified in a single column. Blue color: gene deletion; red color: gene amplification; green and black bars: mutations; gray color: no alteration. Up to 10% of TP53 gene deletion can be detected. MDM2 amplification is found predominantly in tumours that express wild-type TP53. Data from http://www.cbioportal.org/index.do
Oncogenesis Mutation of RB1, located at chromosome 13q14.2 and TP53 are frequent in osteosarcoma. Deletion or rearrangement of the TP53 gene can reach 20% and are not found in other cancer types.
  
Entity Brain Tumours
Disease Case per year (thousands) 256; death per year (thousands) 189 (worldwide ranks 17/11) Glioblastoma (GBM), also known as glioblastoma and grade IV astrocytoma, is the most common and most aggressive form and represent 15% of brain tumours. There are two subtypes of GBM: de novo (new or primary) and secondary. De novo tumours are the most common (90%) and are very aggressive. Secondary GBM (10%) typically start as low-grade or mid-grade astrocytoma and eventually transform into malignant, rapidly growing GBM.
Oncogenesis TP53 mutation is an early and frequent (over 60%) event in secondary glioblastomas while it is rare in primary glioblastomas (less than 10%). Primary glioblastomas display a high frequency of mdm2 amplification which is mutually exclusive to TP53 mutations. Isocitrate dehydrogenase 1 ( IDH1) mutations are frequent in secondary glioblastomas (60-70%) and seems to co-occur with TP53 mutations.
  
Entity Chronic lymphocytic leukaemia (CLL)
Disease Chronic lymphocytic leukaemia (CLL) represents the most common leukaemia in the Western world; it accounts for ~40% of all adult leukaemia's.
Prognosis TP53 mutations are associated with a poor response to therapy.
Cytogenetics CLL patients have acquired chromosomal abnormalities such as: deletion 13q; deletion 11q; trisomy 12 and deletion 17p
 
TP53 The frequency of TP53 mutation is low during the asymptomatic phase. Deep sequencing can pick up rare oligoclonal TP53 mutations that are selected during the progression of the disease. The frequency of TP53 mutation can reach 40 to 50% during progressive disease and are associated with therapy resistance and relapse leading to patients with a high frequency of TP53 mutation and poor prognosis.
Oncogenesis TP53 mutations are infrequent in the early phase of the disease and are mostly found in patients in progressive disease or with relapse/refractory disease.
  
Entity Non-Hodgkin lymphoma
Disease Follicular lymphoma (FL) and diffuse large B-cell lymphoma (DLBCL) are the two most common non-Hodgkin lymphomas (NHLs).
Prognosis TP53 mutation is an independent marker of poor prognosis in patients with diffuse large B-cell lymphoma (DLBCL) treated with cyclophosphamide, hydroxydaunorubicin, vincristine, and prednisone (CHOP) therapy
Oncogenesis Both FL and DLCBL are characterized by a high frequency of mutations in genes associated with chromatin modification such as KMT2D /MLL2 or . Frequency of TP53 mutation in DLBCL range between 20 and 80%. This large range is due to the heterogeneity of the various cohorts as TP53 mutations are more frequent in patients with refractory DLBCL.
  
Entity Burkitt lymphoma
Disease Burkitt lymphoma (BL) is an uncommon form of aggressive lymphoma. Three subtypes of Burkitt lymphoma are recognized: the endemic form, occurring primarily in Africa and associated with the Epstein-Barr virus (EBV); the sporadic form, representing less than 3 % of all non-Hodgkin lymphomas (NHL); and the immunodeficiency-associated form, occurring primarily in HIV-infected patients.
Oncogenesis BL is characterized by chromosomal translocations leading to the overexpression of myc. The most common rearrangement is t(8;14)(q24;q32), which accounts for most cases and involve MYC and . Other frequently mutated genes are ID3, ARID1A, SMARCA4 and TP53 which is inactivated in 40 to 50% of BL.
  
Entity Myelodysplastic syndromes
Disease Myelodysplastic syndromes (MDS) describe a heterogeneous group of bone marrow disorders that predominate in the elderly. These patients present with a dysplastic bone marrow morphology and variable cytopenias, and they have an increased risk of transformation to acute myeloid leukaemia (AML)
Oncogenesis The frequency of TP53 mutation in MDS is low but associated with a poor prognosis.
  
Entity Acute myeloid leukaemia
Disease Acute myeloid leukemia (AML) is a biologically heterogeneous disease that can be classified into 3 distinct groups: secondary AML (s-AML) represents transformation of an antecedent diagnosis of myelodysplastic syndrome (MDS) or myelo-proliferative neoplasm (MPN), therapy-related AML (t-AML) develops as a late complication in patients with prior exposure to therapies, and de novo AML arises in the absence of an identified exposure or prodromal stem cell disorder.
Oncogenesis The most frequently mutated gene in AML are FLT3, NPM1 and DNMT3A. The frequency of TP53 mutation does not exceed 10% in de novo AML. In t-AML or s-AML, the frequency of TP53 mutation can reach 30% and is associated with a poor prognosis.
  
Entity Li-Fraumeni syndrome (LFS)
Disease Autosomal dominant condition, cancer-prone disease, Li-Fraumeni syndrome (LFS) is defined by the existence of a proband with early onset sarcoma and a first degree relative with cancer before 45 years, plus another first/second degree relative with cancer at before 45 years or sarcoma at any age.
Other extended criteria have been proposed to provide better guidelines for TP53 genetic testing:
Birch definition : (1) a proband with any childhood cancer or sarcoma, brain tumour, or adrenocortical carcinoma diagnosed before age 45 years and (2) a first- or second-degree relative with a typical Li-Fraumeni cancer (sarcoma, breast cancer, brain tumour, adrenocortical carcinoma, or leukaemia) at any age and (3) a first- or second-degree relative with any cancer before age 60 years.
Eels definition: Two first- or second-degree relatives with Li-Fraumeni-related malignancies (sarcoma, breast cancer, brain tumour, leukaemia, adrenocortical tumour, melanoma, prostate cancer, pancreatic cancer) at any age.
Chompret definition: A proband who has (1) a tumour belonging to the Li-Fraumeni tumour spectrum (soft-tissue sarcoma, osteosarcoma, premenopausal breast cancer, brain tumour, adrenocortical carcinoma, leukemia, or bronchoalveolar lung cancer) before age 46 years and (2) at least one first- or second-degree relative with a Li-Fraumeni tumour (except breast cancer if the proband has breast cancer) before age 56 years or with multiple tumours or a proband with multiple tumours (except multiple breast tumours), 2 of which belong to the Li-Fraumeni tumour spectrum and the first of which occurred before age 46 years or A proband who is diagnosed with adrenocortical carcinoma or choroid plexus tumours, irrespective of family history.
Prognosis Most common cancer in Li-Fraumeni children (before the age of 10 years) are: soft tissue sarcoma, brain tumours and adrenocortical carcinomas; osteosarcoma predominates in adolescents; afterwards, female breast cancer, soft tissue sarcomas and brain tumours prevail, and other less frequent cancers such as leukemias or colon carcinomas are also observed. Multiple primary cancers are quite characteristic of Li- Fraumeni syndrome but may also be representative of Bloom's syndrome. Cancers in this disease, as in other cancer-prone diseases, often occur early in life: 50% of patients aged 30 years have had a cancer (i.e. penetrance is 50%, according to this disease definition), and penetrance is 90% at age 60 years.
Oncogenesis Approximately 70% of families with LFS have a mutation in the TP53 gene. Most of these variants are missense mutations similar to those found in colorectal carcinoma with a high frequency of mutations at CpG dinucleotides.
  

Bibliography

25 Years of p53 Research
Editors: Pierre Hainaut, Klas G. Wiman
ISBN: 978-1-4020-2920-2 (2005) Springer
 
Li-Fraumeni syndrome--a molecular and clinical review
Varley JM, Evans DG, Birch JM
Br J Cancer 1997;76(1):1-14
PMID 9218725
 
Dial 9-1-1 for p53: mechanisms of p53 activation by cellular stress
Ljungman M
Neoplasia 2000 May-Jun;2(3):208-25
PMID 10935507
 
Surfing the p53 network
Vogelstein B, Lane D, Levine AJ
Nature 2000 Nov 16;408(6810):307-10
PMID 11099028
 
p53: death star
Vousden KH
Cell 2000 Nov 22;103(5):691-4
PMID 11114324
 
P63 and P73: P53 mimics, menaces and more
Yang A, McKeon F
Nat Rev Mol Cell Biol 2000 Dec;1(3):199-207
PMID 11252895
 
Assessing TP53 status in human tumours to evaluate clinical outcome
Soussi T, Béroud C
Nat Rev Cancer 2001 Dec;1(3):233-40
PMID 11902578
 
The evolution of diverse biological responses to DNA damage: insights from yeast and p53
Wahl GM, Carr AM
Nat Cell Biol 2001 Dec;3(12):E277-86
PMID 11781586
 
p73: Friend or foe in tumorigenesis
Melino G, De Laurenzi V, Vousden KH
Nat Rev Cancer 2002 Aug;2(8):605-15
PMID 12154353
 
Li-Fraumeni and related syndromes: correlation between tumor type, family structure, and TP53 genotype
Olivier M, Goldgar DE, Sodha N, Ohgaki H, Kleihues P, Hainaut P, Eeles RA
Cancer Res 2003 Oct 15;63(20):6643-50
PMID 14583457
 
Focus on the p53 gene and cancer: advances in TP53 mutation research
Soussi T
Hum Mutat 2003 Mar;21(3):173-5
PMID 12619102
 
The p53 pathway: positive and negative feedback loops
Harris SL, Levine AJ
Oncogene 2005 Apr 18;24(17):2899-908
PMID 15838523
 
Transcription-independent pro-apoptotic functions of p53
Moll UM, Wolff S, Speidel D, Deppert W
Curr Opin Cell Biol 2005 Dec;17(6):631-6
PMID 16226451
 
p53 aerobics: the major tumor suppressor fuels your workout
Kruse JP, Gu W
Cell Metab 2006 Jul;4(1):1-3
PMID 16814724
 
p53: more research and more questions
Braithwaite AW, Prives CL
Cell Death Differ 2006 Jun;13(6):877-80
PMID 16708075
 
TP53 mutations in human cancers: functional selection and impact on cancer prognosis and outcomes
Petitjean A, Achatz MI, Borresen-Dale AL, Hainaut P, Olivier M
Oncogene 2007 Apr 2;26(15):2157-65
PMID 17401424
 
Impact of mutant p53 functional properties on TP53 mutation patterns and tumor phenotype: lessons from recent developments in the IARC TP53 database
Petitjean A, Mathe E, Kato S, Ishioka C, Tavtigian SV, Hainaut P, Olivier M
Hum Mutat 2007 Jun;28(6):622-9
PMID 17311302
 
The first 30 years of p53: growing ever more complex
Levine AJ, Oren M
Nat Rev Cancer 2009 Oct;9(10):749-58
PMID 19776744
 
Autophagy regulation by p53
Maiuri MC, Galluzzi L, Morselli E, Kepp O, Malik SA, Kroemer G
Curr Opin Cell Biol 2010 Apr;22(2):181-5
PMID 20044243
 
p53: guardian of ploidy
Aylon Y, Oren M
Mol Oncol 2011 Aug;5(4):315-23
PMID 21852209
 
Metabolic regulation by p53 family members
Berkers CR, Maddocks OD, Cheung EC, Mor I, Vousden KH
Cell Metab 2013 Nov 5;18(5):617-33
PMID 23954639
 
Mutational landscape and significance across 12 major cancer types
Kandoth C, McLellan MD, Vandin F, Ye K, Niu B, Lu C, Xie M, Zhang Q, McMichael JF, Wyczalkowski MA, Leiserson MD, Miller CA, Welch JS, Walter MJ, Wendl MC, Ley TJ, Wilson RK, Raphael BJ, Ding L
Nature 2013 Oct 17;502(7471):333-9
PMID 24132290
 
Impact of neonatal screening and surveillance for the TP53 R337H mutation on early detection of childhood adrenocortical tumors
Custódio G, Parise GA, Kiesel Filho N, Komechen H, Sabbaga CC, Rosati R, Grisa L, Parise IZ, Pianovski MA, Fiori CM, Ledesma JA, Barbosa JR, Figueiredo FR, Sade ER, Ibañez H, Arram SB, Stinghen ST, Mengarelli LR, Figueiredo MM, Carvalho DC, Avilla SG, Woiski TD, Poncio LC, Lima GF, Pontarolo R, Lalli E, Zhou Y, Zambetti GP, Ribeiro RC, Figueiredo BC
J Clin Oncol 2013 Jul 10;31(20):2619-26
PMID 23733769
 
Deciphering signatures of mutational processes operative in human cancer
Alexandrov LB, Nik-Zainal S, Wedge DC, Campbell PJ, Stratton MR
Cell Rep 2013 Jan 31;3(1):246-59
PMID 23318258
 
Unravelling mechanisms of p53-mediated tumour suppression
Bieging KT, Mello SS, Attardi LD
Nat Rev Cancer 2014 May;14(5):359-70
PMID 24739573
 
Mutant p53 in cancer: new functions and therapeutic opportunities
Muller PA, Vousden KH
Cancer Cell 2014 Mar 17;25(3):304-17
PMID 24651012
 
Recommendations for analyzing and reporting TP53 gene variants in the high-throughput sequencing era
Soussi T, Leroy B, Taschner PE
Hum Mutat 2014 Jun;35(6):766-78
 
Locus-specific databases in cancer: what future in a post-genomic era? The TP53 LSDB paradigm
Soussi T
Hum Mutat 2014 Jun;35(6):643-53
PMID 24478183
 
p53 orchestrates between normal differentiation and cancer
Rivlin N, Koifman G, Rotter V
Semin Cancer Biol 2015 Jun;32:10-7
PMID 24406212
 
p53 in survival, death and metabolic health: a lifeguard with a licence to kill
Kruiswijk F, Labuschagne CF, Vousden KH
Nat Rev Mol Cell Biol 2015 Jul;16(7):393-405
PMID 26122615
 
Cancer: A piece of the p53 puzzle
Bieging KT, Attardi LD
Nature 2015 Apr 2;520(7545):37-8
PMID 25799989
 
TP53: an oncogene in disguise
Soussi T, Wiman KG
Cell Death Differ 2015 Aug;22(8):1239-49
PMID 26024390
 
p53 in survival, death and metabolic health: a lifeguard with a licence to kill
Kruiswijk F, Labuschagne CF, Vousden KH
Nat Rev Mol Cell Biol 2015 Jul;16(7):393-405
PMID 26122615
 
Surveillance recommendations for patients with germline TP53 mutations
Ballinger ML, Mitchell G, Thomas DM
Curr Opin Oncol 2015 Jul;27(4):332-7
PMID 26049273
 

Citation

This paper should be referenced as such :
Soussi T
TP53 (Tumour protein p53 (Li-Fraumeni syndrome));
Atlas Genet Cytogenet Oncol Haematol. in press
On line version : http://AtlasGeneticsOncology.org/Genes/P53ID88.html
History of this paper:
Hamelin, R ; Huret, JL. P53 (protein 53 kDa). Atlas Genet Cytogenet Oncol Haematol. 1998;2(4):119-119.
http://documents.irevues.inist.fr/bitstream/handle/2042/37452/07-1998-P53ID88.pdf
Hamelin, R ; Huret, JL. P53 (protein 53 kDa). Atlas Genet Cytogenet Oncol Haematol. 1999;3(1):8-10.
http://documents.irevues.inist.fr/bitstream/handle/2042/37475/10-1998-P53ID88.pdf
Soussi, T. P53 (protein 53 kDa). Atlas Genet Cytogenet Oncol Haematol. 2002;6(2):90-92.
http://documents.irevues.inist.fr/bitstream/handle/2042/37831/12-2001-P53ID88.pdf
Soussi, T. P53 (protein 53 kDa). Atlas Genet Cytogenet Oncol Haematol. 2003;7(1):6-9.
http://documents.irevues.inist.fr/bitstream/handle/2042/37921/10-2002-P53ID88.pdf
Olivier, Magali. TP53 (tumor protein p53 (Li-Fraumeni syndrome)) - an update. Atlas Genet Cytogenet Oncol Haematol. 2007;11(4):276-280.
http://documents.irevues.inist.fr/bitstream/handle/2042/15937/12-2007-P53ID88.pdf


Other Leukemias implicated (Data extracted from papers in the Atlas) [ 39 ]
  Classification of B-cell chronic lymphoproliferative disorders (CLD)
Classification of B-cell non-Hodgkin lymphomas (NHL)
Burkitt's lymphoma (BL)
Classification of myelodysplastic syndromes 2015
Classification of myelodysplasic syndromes 1999
Chronic lymphocytic leukaemia (CLL)
Chronic myelogenous leukaemia (CML)
Chronic Myelomonocytic Leukemia (CMML)
del(17p) in myeloid malignancies
del(17p) in non-Hodgkin's lymphoma (NHL)
dic(17;20)(p11.2;q11.2)
Diffuse large cell lymphoma
Hairy Cell Leukemia (HCL) and Hairy Cell Leukemia Variant (HCL-V)
Hodgkin lymphoma
i(17q) solely in myeloid malignancies
Marginal Zone B-cell lymphoma
MLL amplification in leukemia
Nasal T cell lymphoma
Peripheral T-cell lymphoma not otherwise specified (PTCL-NOS)
Plasma cell leukemia (PCL)
Small lymphocytic lymphoma
t(1;3)(q25;q27) GAS5/BCL6
t(1;9)(p13;p12) PAX5/HIPK1
t(3;3)(q27;q27) ST6GAL1/BCL6;del(3)(q27q27) ST6GAL1/BCL6
t(3;5)(q25;q34) NPM1/MLF1
t(3;6)(q27;p22) HIST1H4I/BCL6
t(3;6)(q27;q14) SNHG5/BCL6
t(3;6)(q27;q15) ?/BCL6
t(3;7)(q27;q32) MIR29A/BCL6
t(3;7)(q27;q32) FRA7H/BCL6
t(3;9)(q27;p13) GRHPR/BCL6
t(3;9)(q27;p24) DMRT1/BCL6
t(3;11)(q27;q23) POU2AF1/BCL6
t(3;12)(q27;p12) LRMP/BCL6
t(3;14)(q27;q32) HSP90AA1/BCL6
t(3;19)(q27;q13) NAPA/BCL6
t(9;10)(q34;q22) ZMIZ1/ABL1
Classification of T-Cell disorders

Other Solid tumors implicated (Data extracted from papers in the Atlas) [ 61 ]
  Neuro-Endocrine/Endocrine System: Adrenal cortical carcinoma
Thyroid: Anaplastic (undifferentiated) carcinoma
Nervous system: Astrocytic tumors
Esophagus: Barrett's esophagus, dysplasia and adenocarcinoma
Bladder: Squamous cell carcinoma
Bladder: Urothelial carcinomas
Breast tumors : an overview
Uterus: Carcinoma of the cervix
Colon: Colorectal adenocarcinoma
Bone: Conventional Osteosarcoma
Bone: Dedifferentiated chondrosarcoma
Soft Tissues: Desmoplastic small round cell tumor
Breast: Ductal carcinoma
Nervous system: Ependymomas
Fallopian tube tumors: an overview
Gallbladder: Carcinoma of the gallbladder and extrahepatic bile ducts
Gastric Tumors: an overview
Nervous System: Glioma: an overview
Head and Neck: Squamous cell carcinoma: an overview
Head and Neck: Epidermoid carcinoma
Liver: Hepatoblastoma
Liver: Hepatocellular carcinoma
Liver: Combined hepatocellular and cholangiocarcinoma
Gallbladder: Intrahepatic cholangiocarcinoma
Head and Neck: Laryngeal tumors: an overview
Head and Neck: Laryngeal squamous cell carcinoma
Lung: Non-small cell carcinoma
Lung: small cell cancer
Lung tumors: an overview
Testis: Germ cell tumors
Thyroid: Medullary carcinoma
Nervous system: Medulloblastoma
Liver: Nested stromal epithelial tumor
Head and Neck: Oral leukoplakia
Head and Neck: Oral squamous cell carcinoma
Bone: Osteoblastoma
Bone: Osteosarcoma
Ovarian tumours : an overview
Ovary: Sex cord-stromal tumors
Ovary: Choriocarcinoma
Ovary: Epithelial tumors
Pancreatic tumors: an overview
Penile tumors: an overview
Nervous system: Peripheral nerve sheath tumors
Lung: Pleuropulmonary blastoma
Prostate tumors: an overview
Kidney: Renal cell carcinoma
Soft Tissues: Rhabdomyosarcoma
Head and Neck: Salivary gland tumors: an overview
Skin: Melanoma
Soft tissue tumors: an overview
Testis: Spermatocytic seminoma
Squamous cell cancer
Kidney: Clear cell sarcoma with t(10;17)(q22;p13) YWHAE/NUTM2E
Head and Neck: Thymus: Thymoma: an overview
Lung: Translocations in Adenocarcinoma
Lung: Translocations in Small Cell Carcinoma
Lung: Translocations in Squamous Cell Carcinoma
Uterus Tumours: an Overview
Eye: Posterior uveal melanoma
Soft Tissues: Well-differentiated liposarcoma
Kidney: Nephroblastoma (Wilms tumor)

Other Cancer prone implicated (Data extracted from papers in the Atlas) [ 5 ]
  Dysplastic nevus syndrome (DNS) Familial nervous system tumour syndromes Hereditary breast cancer Hereditary pancreatic cancer Li-Fraumeni syndrome

External links

Nomenclature
HGNC (Hugo)TP53   11998
Cards
AtlasP53ID88
Entrez_Gene (NCBI)TP53  7157  tumor protein p53
GeneCards (Weizmann)TP53
Ensembl hg19 (Hinxton)ENSG00000141510 [Gene_View]  chr17:7571720-7590868 [Contig_View]  TP53 [Vega]
Ensembl hg38 (Hinxton)ENSG00000141510 [Gene_View]  chr17:7571720-7590868 [Contig_View]  TP53 [Vega]
ICGC DataPortalENSG00000141510
TCGA cBioPortalTP53
AceView (NCBI)TP53
Genatlas (Paris)TP53
WikiGenes7157
SOURCE (Princeton)TP53
Genomic and cartography
GoldenPath hg19 (UCSC)TP53  -     chr17:7571720-7590868 -  17p13.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)TP53  -     17p13.1   [Description]    (hg38-Dec_2013)
EnsemblTP53 - 17p13.1 [CytoView hg19]  TP53 - 17p13.1 [CytoView hg38]
Mapping of homologs : NCBITP53 [Mapview hg19]  TP53 [Mapview hg38]
OMIM114480   114500   114550   137800   151623   191170   202300   259500   260350   260500   607107   614740   
Gene and transcription
Genbank (Entrez)AB082923 AF052180 AF307851 AK223026 AK225838
RefSeq transcript (Entrez)NM_000546 NM_001126112 NM_001126113 NM_001126114 NM_001126115 NM_001126116 NM_001126117 NM_001126118 NM_001276695 NM_001276696 NM_001276697 NM_001276698 NM_001276699 NM_001276760 NM_001276761
RefSeq genomic (Entrez)NC_000017 NC_018928 NG_017013 NT_010718 NW_004929405
Consensus coding sequences : CCDS (NCBI)TP53
Cluster EST : UnigeneHs.740601 [ NCBI ]
CGAP (NCI)Hs.740601
Alternative Splicing GalleryENSG00000141510
Gene ExpressionTP53 [ NCBI-GEO ]   TP53 [ EBI - ARRAY_EXPRESS ]   TP53 [ SEEK ]   TP53 [ MEM ]
Gene Expression Viewer (FireBrowse)TP53 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)7157
GTEX Portal (Tissue expression)TP53
Protein : pattern, domain, 3D structure
UniProt/SwissProtP04637 (Uniprot)
NextProtP04637  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP04637
Splice isoforms : SwissVarP04637 (Swissvar)
PhosPhoSitePlusP04637
Domaine pattern : Prosite (Expaxy)P53 (PS00348)   
Domains : Interpro (EBI)p53-like_TF_DNA-bd    p53/RUNT-type_TF_DNA-bd    p53_DNA-bd    p53_tetrameristn    p53_transactivation_domain    p53_tumour_suppressor   
Domain families : Pfam (Sanger)P53 (PF00870)    P53_TAD (PF08563)    P53_tetramer (PF07710)   
Domain families : Pfam (NCBI)pfam00870    pfam08563    pfam07710   
DMDM Disease mutations7157
Blocks (Seattle)TP53
PDB (SRS)1A1U    1AIE    1C26    1DT7    1GZH    1H26    1HS5    1JSP    1KZY    1MA3    1OLG    1OLH    1PES    1PET    1SAE    1SAF    1SAK    1SAL    1TSR    1TUP    1UOL    1XQH    1YC5    1YCQ    1YCR    1YCS    2AC0    2ADY    2AHI    2ATA    2B3G    2BIM    2BIN    2BIO    2BIP    2BIQ    2F1X    2FEJ    2FOJ    2FOO    2GS0    2H1L    2H2D    2H2F    2H4F    2H4H    2H4J    2H59    2J0Z    2J10    2J11    2J1W    2J1X    2J1Y    2J1Z    2J20    2J21    2K8F    2L14    2LY4    2MEJ    2MWO    2MWP    2MWY    2MZD    2OCJ    2PCX    2RUK    2VUK    2WGX    2X0U    2X0V    2X0W    2XWR    2YBG    2YDR    2Z5S    2Z5T    3D05    3D06    3D07    3D08    3D09    3D0A    3DAB    3DAC    3IGK    3IGL    3KMD    3KZ8    3LW1    3OQ5    3PDH    3Q01    3Q05    3Q06    3SAK    3TG5    3TS8    3ZME    4AGL    4AGM    4AGN    4AGO    4AGP    4AGQ    4BUZ    4BV2    4HFZ    4HJE    4IBQ    4IBS    4IBT    4IBU    4IBV    4IBW    4IBY    4IBZ    4IJT    4KVP    4LO9    4LOE    4LOF    4MZI    4MZR    4QO1    4RP6    4RP7    4X34    4XR8    4ZZJ    5A7B    5AB9    5ABA    5AOI    5AOJ    5AOK    5AOL    5AOM    5ECG   
PDB (PDBSum)1A1U    1AIE    1C26    1DT7    1GZH    1H26    1HS5    1JSP    1KZY    1MA3    1OLG    1OLH    1PES    1PET    1SAE    1SAF    1SAK    1SAL    1TSR    1TUP    1UOL    1XQH    1YC5    1YCQ    1YCR    1YCS    2AC0    2ADY    2AHI    2ATA    2B3G    2BIM    2BIN    2BIO    2BIP    2BIQ    2F1X    2FEJ    2FOJ    2FOO    2GS0    2H1L    2H2D    2H2F    2H4F    2H4H    2H4J    2H59    2J0Z    2J10    2J11    2J1W    2J1X    2J1Y    2J1Z    2J20    2J21    2K8F    2L14    2LY4    2MEJ    2MWO    2MWP    2MWY    2MZD    2OCJ    2PCX    2RUK    2VUK    2WGX    2X0U    2X0V    2X0W    2XWR    2YBG    2YDR    2Z5S    2Z5T    3D05    3D06    3D07    3D08    3D09    3D0A    3DAB    3DAC    3IGK    3IGL    3KMD    3KZ8    3LW1    3OQ5    3PDH    3Q01    3Q05    3Q06    3SAK    3TG5    3TS8    3ZME    4AGL    4AGM    4AGN    4AGO    4AGP    4AGQ    4BUZ    4BV2    4HFZ    4HJE    4IBQ    4IBS    4IBT    4IBU    4IBV    4IBW    4IBY    4IBZ    4IJT    4KVP    4LO9    4LOE    4LOF    4MZI    4MZR    4QO1    4RP6    4RP7    4X34    4XR8    4ZZJ    5A7B    5AB9    5ABA    5AOI    5AOJ    5AOK    5AOL    5AOM    5ECG   
PDB (IMB)1A1U    1AIE    1C26    1DT7    1GZH    1H26    1HS5    1JSP    1KZY    1MA3    1OLG    1OLH    1PES    1PET    1SAE    1SAF    1SAK    1SAL    1TSR    1TUP    1UOL    1XQH    1YC5    1YCQ    1YCR    1YCS    2AC0    2ADY    2AHI    2ATA    2B3G    2BIM    2BIN    2BIO    2BIP    2BIQ    2F1X    2FEJ    2FOJ    2FOO    2GS0    2H1L    2H2D    2H2F    2H4F    2H4H    2H4J    2H59    2J0Z    2J10    2J11    2J1W    2J1X    2J1Y    2J1Z    2J20    2J21    2K8F    2L14    2LY4    2MEJ    2MWO    2MWP    2MWY    2MZD    2OCJ    2PCX    2RUK    2VUK    2WGX    2X0U    2X0V    2X0W    2XWR    2YBG    2YDR    2Z5S    2Z5T    3D05    3D06    3D07    3D08    3D09    3D0A    3DAB    3DAC    3IGK    3IGL    3KMD    3KZ8    3LW1    3OQ5    3PDH    3Q01    3Q05    3Q06    3SAK    3TG5    3TS8    3ZME    4AGL    4AGM    4AGN    4AGO    4AGP    4AGQ    4BUZ    4BV2    4HFZ    4HJE    4IBQ    4IBS    4IBT    4IBU    4IBV    4IBW    4IBY    4IBZ    4IJT    4KVP    4LO9    4LOE    4LOF    4MZI    4MZR    4QO1    4RP6    4RP7    4X34    4XR8    4ZZJ    5A7B    5AB9    5ABA    5AOI    5AOJ    5AOK    5AOL    5AOM    5ECG   
PDB (RSDB)1A1U    1AIE    1C26    1DT7    1GZH    1H26    1HS5    1JSP    1KZY    1MA3    1OLG    1OLH    1PES    1PET    1SAE    1SAF    1SAK    1SAL    1TSR    1TUP    1UOL    1XQH    1YC5    1YCQ    1YCR    1YCS    2AC0    2ADY    2AHI    2ATA    2B3G    2BIM    2BIN    2BIO    2BIP    2BIQ    2F1X    2FEJ    2FOJ    2FOO    2GS0    2H1L    2H2D    2H2F    2H4F    2H4H    2H4J    2H59    2J0Z    2J10    2J11    2J1W    2J1X    2J1Y    2J1Z    2J20    2J21    2K8F    2L14    2LY4    2MEJ    2MWO    2MWP    2MWY    2MZD    2OCJ    2PCX    2RUK    2VUK    2WGX    2X0U    2X0V    2X0W    2XWR    2YBG    2YDR    2Z5S    2Z5T    3D05    3D06    3D07    3D08    3D09    3D0A    3DAB    3DAC    3IGK    3IGL    3KMD    3KZ8    3LW1    3OQ5    3PDH    3Q01    3Q05    3Q06    3SAK    3TG5    3TS8    3ZME    4AGL    4AGM    4AGN    4AGO    4AGP    4AGQ    4BUZ    4BV2    4HFZ    4HJE    4IBQ    4IBS    4IBT    4IBU    4IBV    4IBW    4IBY    4IBZ    4IJT    4KVP    4LO9    4LOE    4LOF    4MZI    4MZR    4QO1    4RP6    4RP7    4X34    4XR8    4ZZJ    5A7B    5AB9    5ABA    5AOI    5AOJ    5AOK    5AOL    5AOM    5ECG   
Structural Biology KnowledgeBase1A1U    1AIE    1C26    1DT7    1GZH    1H26    1HS5    1JSP    1KZY    1MA3    1OLG    1OLH    1PES    1PET    1SAE    1SAF    1SAK    1SAL    1TSR    1TUP    1UOL    1XQH    1YC5    1YCQ    1YCR    1YCS    2AC0    2ADY    2AHI    2ATA    2B3G    2BIM    2BIN    2BIO    2BIP    2BIQ    2F1X    2FEJ    2FOJ    2FOO    2GS0    2H1L    2H2D    2H2F    2H4F    2H4H    2H4J    2H59    2J0Z    2J10    2J11    2J1W    2J1X    2J1Y    2J1Z    2J20    2J21    2K8F    2L14    2LY4    2MEJ    2MWO    2MWP    2MWY    2MZD    2OCJ    2PCX    2RUK    2VUK    2WGX    2X0U    2X0V    2X0W    2XWR    2YBG    2YDR    2Z5S    2Z5T    3D05    3D06    3D07    3D08    3D09    3D0A    3DAB    3DAC    3IGK    3IGL    3KMD    3KZ8    3LW1    3OQ5    3PDH    3Q01    3Q05    3Q06    3SAK    3TG5    3TS8    3ZME    4AGL    4AGM    4AGN    4AGO    4AGP    4AGQ    4BUZ    4BV2    4HFZ    4HJE    4IBQ    4IBS    4IBT    4IBU    4IBV    4IBW    4IBY    4IBZ    4IJT    4KVP    4LO9    4LOE    4LOF    4MZI    4MZR    4QO1    4RP6    4RP7    4X34    4XR8    4ZZJ    5A7B    5AB9    5ABA    5AOI    5AOJ    5AOK    5AOL    5AOM    5ECG   
SCOP (Structural Classification of Proteins)1A1U    1AIE    1C26    1DT7    1GZH    1H26    1HS5    1JSP    1KZY    1MA3    1OLG    1OLH    1PES    1PET    1SAE    1SAF    1SAK    1SAL    1TSR    1TUP    1UOL    1XQH    1YC5    1YCQ    1YCR    1YCS    2AC0    2ADY    2AHI    2ATA    2B3G    2BIM    2BIN    2BIO    2BIP    2BIQ    2F1X    2FEJ    2FOJ    2FOO    2GS0    2H1L    2H2D    2H2F    2H4F    2H4H    2H4J    2H59    2J0Z    2J10    2J11    2J1W    2J1X    2J1Y    2J1Z    2J20    2J21    2K8F    2L14    2LY4    2MEJ    2MWO    2MWP    2MWY    2MZD    2OCJ    2PCX    2RUK    2VUK    2WGX    2X0U    2X0V    2X0W    2XWR    2YBG    2YDR    2Z5S    2Z5T    3D05    3D06    3D07    3D08    3D09    3D0A    3DAB    3DAC    3IGK    3IGL    3KMD    3KZ8    3LW1    3OQ5    3PDH    3Q01    3Q05    3Q06    3SAK    3TG5    3TS8    3ZME    4AGL    4AGM    4AGN    4AGO    4AGP    4AGQ    4BUZ    4BV2    4HFZ    4HJE    4IBQ    4IBS    4IBT    4IBU    4IBV    4IBW    4IBY    4IBZ    4IJT    4KVP    4LO9    4LOE    4LOF    4MZI    4MZR    4QO1    4RP6    4RP7    4X34    4XR8    4ZZJ    5A7B    5AB9    5ABA    5AOI    5AOJ    5AOK    5AOL    5AOM    5ECG   
CATH (Classification of proteins structures)1A1U    1AIE    1C26    1DT7    1GZH    1H26    1HS5    1JSP    1KZY    1MA3    1OLG    1OLH    1PES    1PET    1SAE    1SAF    1SAK    1SAL    1TSR    1TUP    1UOL    1XQH    1YC5    1YCQ    1YCR    1YCS    2AC0    2ADY    2AHI    2ATA    2B3G    2BIM    2BIN    2BIO    2BIP    2BIQ    2F1X    2FEJ    2FOJ    2FOO    2GS0    2H1L    2H2D    2H2F    2H4F    2H4H    2H4J    2H59    2J0Z    2J10    2J11    2J1W    2J1X    2J1Y    2J1Z    2J20    2J21    2K8F    2L14    2LY4    2MEJ    2MWO    2MWP    2MWY    2MZD    2OCJ    2PCX    2RUK    2VUK    2WGX    2X0U    2X0V    2X0W    2XWR    2YBG    2YDR    2Z5S    2Z5T    3D05    3D06    3D07    3D08    3D09    3D0A    3DAB    3DAC    3IGK    3IGL    3KMD    3KZ8    3LW1    3OQ5    3PDH    3Q01    3Q05    3Q06    3SAK    3TG5    3TS8    3ZME    4AGL    4AGM    4AGN    4AGO    4AGP    4AGQ    4BUZ    4BV2    4HFZ    4HJE    4IBQ    4IBS    4IBT    4IBU    4IBV    4IBW    4IBY    4IBZ    4IJT    4KVP    4LO9    4LOE    4LOF    4MZI    4MZR    4QO1    4RP6    4RP7    4X34    4XR8    4ZZJ    5A7B    5AB9    5ABA    5AOI    5AOJ    5AOK    5AOL    5AOM    5ECG   
SuperfamilyP04637
Human Protein AtlasENSG00000141510
Peptide AtlasP04637
HPRD01859
IPIIPI00025087   IPI00375319   IPI00973801   IPI01009016   IPI01009039   IPI01008713   IPI00796188   IPI00894418   IPI00895905   IPI01018116   IPI00902894   IPI00965012   IPI00816804   IPI01011775   IPI00967077   IPI00968201   
Protein Interaction databases
DIP (DOE-UCLA)P04637
IntAct (EBI)P04637
FunCoupENSG00000141510
BioGRIDTP53
STRING (EMBL)TP53
ZODIACTP53
Ontologies - Pathways
QuickGOP04637
Ontology : AmiGOnegative regulation of transcription from RNA polymerase II promoter  negative regulation of transcription from RNA polymerase II promoter  DNA strand renaturation  nuclear chromatin  RNA polymerase II transcription factor activity, sequence-specific DNA binding  core promoter sequence-specific DNA binding  RNA polymerase II transcription factor binding  transcriptional activator activity, RNA polymerase II transcription regulatory region sequence-specific binding  protease binding  p53 binding  DNA binding  chromatin binding  damaged DNA binding  double-stranded DNA binding  transcription factor activity, sequence-specific DNA binding  copper ion binding  protein binding  ATP binding  nucleus  nucleoplasm  nucleoplasm  replication fork  transcription factor TFIID complex  nucleolus  cytoplasm  mitochondrion  mitochondrial matrix  endoplasmic reticulum  cytosol  cytosol  base-excision repair  nucleotide-excision repair  regulation of transcription, DNA-templated  transcription from RNA polymerase II promoter  protein complex assembly  cellular response to DNA damage stimulus  DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest  DNA damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediator  ER overload response  cell cycle arrest  cell cycle arrest  Ras protein signal transduction  multicellular organism development  cell aging  protein localization  transcription factor binding  zinc ion binding  cell proliferation  negative regulation of cell proliferation  negative regulation of cell proliferation  negative regulation of cell proliferation  determination of adult lifespan  response to X-ray  response to gamma radiation  positive regulation of gene expression  viral process  nuclear matrix  nuclear body  PML body  protein sumoylation  enzyme binding  protein kinase binding  protein phosphatase binding  cell differentiation  negative regulation of cell growth  DNA damage response, signal transduction by p53 class mediator  DNA damage response, signal transduction by p53 class mediator  receptor tyrosine kinase binding  positive regulation of histone deacetylation  chromatin assembly  mitotic G1 DNA damage checkpoint  ubiquitin protein ligase binding  positive regulation of protein oligomerization  cellular protein localization  cellular response to UV  histone acetyltransferase binding  cellular response to drug  cellular response to glucose starvation  intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator  identical protein binding  regulation of apoptotic process  regulation of apoptotic process  positive regulation of apoptotic process  negative regulation of apoptotic process  negative regulation of apoptotic process  entrainment of circadian clock by photoperiod  proteasome-mediated ubiquitin-dependent protein catabolic process  protein complex  positive regulation of neuron apoptotic process  sequence-specific DNA binding  protein self-association  transcription regulatory region DNA binding  negative regulation of transcription, DNA-templated  negative regulation of transcription, DNA-templated  positive regulation of transcription, DNA-templated  positive regulation of transcription, DNA-templated  positive regulation of transcription from RNA polymerase II promoter  positive regulation of transcription from RNA polymerase II promoter  positive regulation of transcription from RNA polymerase II promoter  response to antibiotic  positive regulation of protein export from nucleus  regulation of mitochondrial membrane permeability  protein heterodimerization activity  protein N-terminus binding  negative regulation of fibroblast proliferation  circadian behavior  positive regulation of peptidyl-tyrosine phosphorylation  chaperone binding  negative regulation of helicase activity  protein tetramerization  protein phosphatase 2A binding  negative regulation of telomerase activity  positive regulation of thymocyte apoptotic process  positive regulation of cell cycle arrest  cellular response to hypoxia  cellular response to ionizing radiation  intrinsic apoptotic signaling pathway by p53 class mediator  positive regulation of release of cytochrome c from mitochondria  replicative senescence  oxidative stress-induced premature senescence  intrinsic apoptotic signaling pathway  oligodendrocyte apoptotic process  positive regulation of execution phase of apoptosis  positive regulation of protein insertion into mitochondrial membrane involved in apoptotic signaling pathway  regulation of signal transduction by p53 class mediator  regulation of cell cycle G2/M phase transition  positive regulation of transcription from RNA polymerase II promoter in response to endoplasmic reticulum stress  positive regulation of reactive oxygen species metabolic process  positive regulation of intrinsic apoptotic signaling pathway  
Ontology : EGO-EBInegative regulation of transcription from RNA polymerase II promoter  negative regulation of transcription from RNA polymerase II promoter  DNA strand renaturation  nuclear chromatin  RNA polymerase II transcription factor activity, sequence-specific DNA binding  core promoter sequence-specific DNA binding  RNA polymerase II transcription factor binding  transcriptional activator activity, RNA polymerase II transcription regulatory region sequence-specific binding  protease binding  p53 binding  DNA binding  chromatin binding  damaged DNA binding  double-stranded DNA binding  transcription factor activity, sequence-specific DNA binding  copper ion binding  protein binding  ATP binding  nucleus  nucleoplasm  nucleoplasm  replication fork  transcription factor TFIID complex  nucleolus  cytoplasm  mitochondrion  mitochondrial matrix  endoplasmic reticulum  cytosol  cytosol  base-excision repair  nucleotide-excision repair  regulation of transcription, DNA-templated  transcription from RNA polymerase II promoter  protein complex assembly  cellular response to DNA damage stimulus  DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest  DNA damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediator  ER overload response  cell cycle arrest  cell cycle arrest  Ras protein signal transduction  multicellular organism development  cell aging  protein localization  transcription factor binding  zinc ion binding  cell proliferation  negative regulation of cell proliferation  negative regulation of cell proliferation  negative regulation of cell proliferation  determination of adult lifespan  response to X-ray  response to gamma radiation  positive regulation of gene expression  viral process  nuclear matrix  nuclear body  PML body  protein sumoylation  enzyme binding  protein kinase binding  protein phosphatase binding  cell differentiation  negative regulation of cell growth  DNA damage response, signal transduction by p53 class mediator  DNA damage response, signal transduction by p53 class mediator  receptor tyrosine kinase binding  positive regulation of histone deacetylation  chromatin assembly  mitotic G1 DNA damage checkpoint  ubiquitin protein ligase binding  positive regulation of protein oligomerization  cellular protein localization  cellular response to UV  histone acetyltransferase binding  cellular response to drug  cellular response to glucose starvation  intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator  identical protein binding  regulation of apoptotic process  regulation of apoptotic process  positive regulation of apoptotic process  negative regulation of apoptotic process  negative regulation of apoptotic process  entrainment of circadian clock by photoperiod  proteasome-mediated ubiquitin-dependent protein catabolic process  protein complex  positive regulation of neuron apoptotic process  sequence-specific DNA binding  protein self-association  transcription regulatory region DNA binding  negative regulation of transcription, DNA-templated  negative regulation of transcription, DNA-templated  positive regulation of transcription, DNA-templated  positive regulation of transcription, DNA-templated  positive regulation of transcription from RNA polymerase II promoter  positive regulation of transcription from RNA polymerase II promoter  positive regulation of transcription from RNA polymerase II promoter  response to antibiotic  positive regulation of protein export from nucleus  regulation of mitochondrial membrane permeability  protein heterodimerization activity  protein N-terminus binding  negative regulation of fibroblast proliferation  circadian behavior  positive regulation of peptidyl-tyrosine phosphorylation  chaperone binding  negative regulation of helicase activity  protein tetramerization  protein phosphatase 2A binding  negative regulation of telomerase activity  positive regulation of thymocyte apoptotic process  positive regulation of cell cycle arrest  cellular response to hypoxia  cellular response to ionizing radiation  intrinsic apoptotic signaling pathway by p53 class mediator  positive regulation of release of cytochrome c from mitochondria  replicative senescence  oxidative stress-induced premature senescence  intrinsic apoptotic signaling pathway  oligodendrocyte apoptotic process  positive regulation of execution phase of apoptosis  positive regulation of protein insertion into mitochondrial membrane involved in apoptotic signaling pathway  regulation of signal transduction by p53 class mediator  regulation of cell cycle G2/M phase transition  positive regulation of transcription from RNA polymerase II promoter in response to endoplasmic reticulum stress  positive regulation of reactive oxygen species metabolic process  positive regulation of intrinsic apoptotic signaling pathway  
Pathways : BIOCARTAATM Signaling Pathway [Genes]    Telomeres, Telomerase, Cellular Aging, and Immortality [Genes]    Hypoxia and p53 in the Cardiovascular system [Genes]    Regulation of transcriptional activity by PML [Genes]    BTG family proteins and cell cycle regulation [Genes]    RB Tumor Suppressor/Checkpoint Signaling in response to DNA damage [Genes]    Double Stranded RNA Induced Gene Expression [Genes]    Overview of telomerase protein component gene hTert Transcriptional Regulation [Genes]    Chaperones modulate interferon Signaling Pathway [Genes]    Apoptotic Signaling in Response to DNA Damage [Genes]    Regulation of cell cycle progression by Plk3 [Genes]    CTCF: First Multivalent Nuclear Factor [Genes]    Estrogen-responsive protein Efp controls cell cycle and breast tumors growth [Genes]    Role of BRCA1, BRCA2 and ATR in Cancer Susceptibility [Genes]    Cell Cycle: G1/S Check Point [Genes]    Tumor Suppressor Arf Inhibits Ribosomal Biogenesis [Genes]    Cell Cycle: G2/M Checkpoint [Genes]    p53 Signaling Pathway [Genes]   
Pathways : KEGGMAPK signaling pathway    Cell cycle    p53 signaling pathway    PI3K-Akt signaling pathway    Apoptosis    Wnt signaling pathway    Neurotrophin signaling pathway    Thyroid hormone signaling pathway    Amyotrophic lateral sclerosis (ALS)    Huntington's disease    Hepatitis C    Hepatitis B    Measles    HTLV-I infection    Herpes simplex infection    Epstein-Barr virus infection    Pathways in cancer    Transcriptional misregulation in cancer    Viral carcinogenesis    Proteoglycans in cancer    MicroRNAs in cancer    Colorectal cancer    Pancreatic cancer    Endometrial cancer    Glioma    Prostate cancer    Thyroid cancer    Basal cell carcinoma    Melanoma    Bladder cancer    Chronic myeloid leukemia    Small cell lung cancer    Non-small cell lung cancer   
REACTOMEP04637 [protein]
REACTOME PathwaysR-HSA-69895 Transcriptional activation of cell cycle inhibitor p21 [pathway]
REACTOME PathwaysR-HSA-111448 Activation of NOXA and translocation to mitochondria [pathway]
REACTOME PathwaysR-HSA-5628897 TP53 Regulates Metabolic Genes [pathway]
REACTOME PathwaysR-HSA-2559584 Formation of Senescence-Associated Heterochromatin Foci (SAHF) [pathway]
REACTOME PathwaysR-HSA-2559586 DNA Damage/Telomere Stress Induced Senescence [pathway]
REACTOME PathwaysR-HSA-1912408 Pre-NOTCH Transcription and Translation [pathway]
REACTOME PathwaysR-HSA-349425 Autodegradation of the E3 ubiquitin ligase COP1 [pathway]
REACTOME PathwaysR-HSA-2559580 Oxidative Stress Induced Senescence [pathway]
REACTOME PathwaysR-HSA-69541 Stabilization of p53 [pathway]
REACTOME PathwaysR-HSA-139915 Activation of PUMA and translocation to mitochondria [pathway]
REACTOME PathwaysR-HSA-983231 Factors involved in megakaryocyte development and platelet production [pathway]
REACTOME PathwaysR-HSA-2559585 Oncogene Induced Senescence [pathway]
NDEx Network
Atlas of Cancer Signalling NetworkTP53
Wikipedia pathwaysTP53
Orthology - Evolution
OrthoDB7157
GeneTree (enSembl)ENSG00000141510
Phylogenetic Trees/Animal Genes : TreeFamTP53
Homologs : HomoloGeneTP53
Homology/Alignments : Family Browser (UCSC)TP53
Gene fusions - Rearrangements
Fusion : MitelmanMPRIP/TP53 [17p11.2/17p13.1]  [t(17;17)(p11;p13)]  
Fusion : MitelmanRBBP8/TP53 [18q11.2/17p13.1]  [t(17;18)(p13;q11)]  
Fusion : MitelmanTP53/FARP2 [17p13.1/2q37.3]  [t(2;17)(q37;p13)]  
Fusion : MitelmanTP53/GID4 [17p13.1/17p11.2]  [t(17;17)(p11;p13)]  
Fusion : COSMICTP53 [17p13.1]  -  NTRK1 [1q23.1]  [fusion_1655]  [fusion_1657]  [fusion_1658]  [fusion_1659]  [fusion_1660]  
Fusion: TCGARBBP8 18q11.2 TP53 17p13.1 BLCA
Fusion: TCGATP53 17p13.1 C17orf39 LGG
Fusion: TCGATP53 17p13.1 FARP2 2q37.3 PRAD
Polymorphisms : SNP, variants
NCBI Variation ViewerTP53 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TP53
dbVarTP53
ClinVarTP53
1000_GenomesTP53 
Exome Variant ServerTP53
ExAC (Exome Aggregation Consortium)TP53 (select the gene name)
Genetic variants : HAPMAP7157
Genomic Variants (DGV)TP53 [DGVbeta]
Mutations
ICGC Data PortalTP53 
TCGA Data PortalTP53 
Broad Tumor PortalTP53
OASIS PortalTP53 [ Somatic mutations - Copy number]
Cancer Gene: CensusTP53 
Somatic Mutations in Cancer : COSMICTP53 
intOGen PortalTP53
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
LOVD (Leiden Open Variation Database)MSeqDR-LSDB Mitochondrial Disease Locus Specific Database
BioMutasearch TP53
DgiDB (Drug Gene Interaction Database)TP53
DoCM (Curated mutations)TP53 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)TP53 (select a term)
intoGenTP53
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] 
Diseases
DECIPHER (Syndromes)17:7571720-7590868  ENSG00000141510
CONAN: Copy Number AnalysisTP53 
Mutations and Diseases : HGMDTP53
OMIM114480    114500    114550    137800    151623    191170    202300    259500    260350    260500    607107    614740   
MedgenTP53
Genetic Testing Registry TP53
NextProtP04637 [Medical]
TSGene7157
GENETestsTP53
Huge Navigator TP53 [HugePedia]
snp3D : Map Gene to Disease7157
BioCentury BCIQTP53
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD7157
Chemical/Pharm GKB GenePA36679
Drug Sensitivity TP53
Clinical trialTP53
Miscellaneous
canSAR (ICR)TP53 (select the gene name)
Probes
Litterature
PubMed499 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineTP53
EVEXTP53
GoPubMedTP53
iHOPTP53
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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