| Identity |
| Other names | Hippostasin |
| hK11 | |
| PRSS20 | |
| TLSP | |
| HGNC (Hugo) | KLK11 |
| Location | 19q13.41 |
| Location_base_pair | Starts at 56217305 and ends at 56221682 bp from pter ( according to hg18-Mar_2006) [Mapping] |
| Local_order | Telomere to centromere |
| DNA/RNA |
| Description | The KLK11 gene is about 5.8 Kb in length, consisting of 6 exons and 5 introns. |
| Transcription | Three alternatively spliced variants have been described in the literature: including isoform 1, isoform 2, and isoform 3. Isoform 1 is preferentially expressed in the brain and it encodes a protein of 250 amino acids. Isoform 2 and isoform 3 are mainly expressed in the prostate. Compared to isoform 1, isoform 2 has additional 32 amino acids at the N-terminus and isoform 3 contains extra 25 amino acids inserted in the catalytic triad. Tissue-specific expression of these isoforms is regulated by multiple promoters that locate in the first exon of each isoform. |
| Pseudogene | Not identified so far |
| Protein |
| Description | Full-length KLK11 is composed of a signal peptide (aa 1-50), a propeptide (aa 51-53), and a mature chain (aa 54-282). KLK11 is synthesized as a full-length protein intracellularly. In the secretary pathway, the signal peptide is cleaved and the zymogen is released outside the cells. Upon activation, the propetide is removed to generate the mature active protein. |
| Expression | KLK11 is mainly expressed in epithelial tissues, such as stomach, trachea, and skin, with high levels in the brain and the prostate. KLK11 has also been identified in many biological fluids. Seminal plasma, containing an average of 15 μg/mL of KLK11, is the biological fluid reported to have the most abundant KLK11 so far. Other specimens, including serum, lactating milk, cerebrospinal fluid, and amniotic fluid, all have detectable amounts of KLK11. |
| Localisation | Secreted. |
| Function | The physiology functions of KLK11 and the mechanisms of its involvement in cancer have yet to be determined. Using positional scanning combinatorial tetrapeptide substrate library, it has revealed that KLK11 preferentially cleaves peptide bonds after methionine, arginine, and lysine. However, its physiology substrates remain unidentified. One hypothesis is that KLK11 may be part of a proteolytic cascade consisting of multiple kallikreins (KLKs). Since KLK11 is unable to autoactivate, in the cascade, it is likely that KLK11 is activated by upstream KLKs, then subsequently activate/inactaivate other downstream KLKs or other proteins. Accumulating experimental evidence is in accord with this hypothesis. It has been shown in in vitro experiments that, both KLK12 and KLK14 are able to activate KLK11. Another hypothesis is that KLK11 may be involved in the homeostasis of insulin growth factor. This hypothesis comes from the observation that KLK11 is able to degrade insulin growth factor binding protein 3 (IGFBP3) to facilitate the release of insulin growth factor. KLK11 enzymatic activity is mainly regulated by internal cleavage. In seminal plasma, about half the KLK11 is in the cleaved inactive form. Some abundant serine protease inhibitors present in the circulation or in seminal plasma, such as α1-antitrypsin, protein C inhibitor, α2-antiplasmin, and C1 inhibitor, fail to show rapid inhibition of KLK11. |
| Homology | Human KLK11 protein sequence shares 98% and 82% identity with that of chimpanzee and dog/bovine/mouse/rat, respectively. |
| Mutations |
| Note | No germinal or somatic mutations are identified to be associated with cancer so far. |
| Implicated in |
| Entity | Prostate cancer |
| Disease | A number of investigations have been reported concerning the role of KLK11 as a potential diagnostic biomarker for prostate cancer (CaP). Prostate specific antigen (PSA) is currently the most widely used diagnostic marker for CaP. However, measuring PSA alone is lack of specificity, since some benign prostatic diseases, such as benign prostatic hyperplasia (BPH) and prostatitis, can also have increased serum PSA levels, whereas some CaP patients may have only mild elevation of PSA (4-10 ng/mL). To improve the specificity, a number of additional analyses, such as measuring the molecular forms of PSA, have been proposed. Patients with low free to total PSA ratios are considered to have higher risk of developing CaP. In spite of these efforts, false positive and false negative still occur and doctors frequently need to rely on prostate biopsy to make the final diagnosis. Some investigations have shown that measuring serum KLK11 concentrations may help discriminate CaP from BPH and reduce the number of unnecessary biopsies. Similar to PSA, serum KLK11 concentrations are elevated in the majority of CaP patients. However, compared to the BPH patients, the CaP patients tend to have lower serum KLK11 concentrations and lower KLK11 to total PSA ratios. In those patients that have less than 20% free PSA, measuring KLK11 to total PSA ratio identified 54% to have BPH. As such, it seems that KLK11 to total PSA ratio might be a complementary marker for free PSA percentage and combination of these two markers results in better specificity for CaP. KLK11 might not be superior to PSA in population screening. In a retrospective study, serum KLK11 or KLK11 to PSA ratio showed no advantage over PSA alone to differentiate CaP patients from noncancer individuals whose total PSA levels are in the range of 2.5 to 10 ng/mL. |
| Prognosis | Tissue expression levels of KLK11 may be used as a prognostic indicator for prostate cancer. Lower KLK11 mRNA levels have been found to be associated with higher tumor grade, tumor stage, and Gleason score, suggesting that KLK11 might be able to indicate the aggressiveness of prostate tumors. |
| Cytogenetics | No cytogenetic abnormalities are identified so far. |
| Hybrid/Mutated Gene | Not identified so far. |
| Entity | Ovarian cancer |
| Disease | KLK11 has shown promise as a diagnostic biomarker for ovarian cancer. Earlier studies have revealed that serum KLK11 concentrations are elevated in the majority of ovarian cancer patients. Subsequent investigations further demonstrate that KLK11 is able to distinguish ovarian cancer cases from healthy controls. More importantly, it is less sensitive to benign ovarian diseases than is CA125, the most widely used diagnostic marker for ovarian cancer. Moreover, it has high temporal stability, which implies that it could be used in a longitudinal screening program for early detection. |
| Prognosis | Many investigations have clearly demonstrated that KLK11 has elevated protein levels in primary ovarian tumors than in normal tissue, benign or nonovarian metastatic tumors. In general, higher levels of KLK11 in ovarian tumor extracts are predictive of favorable outcome. They are more likely to be associated with early stage, responsive to chemotherapy, and longer progression free survival. |
| Cytogenetics | No cytogenetic abnormalities are identified so far. |
| Hybrid/Mutated Gene | Not identified so far. |
| Entity | Lung cancer |
| Prognosis | The prognostic role of KLK11 has also been explored in lung cancer both at the mRNA and protein levels. With quantitative PCR, it has shown that KLK11 mRNA levels are lower in tumor tissues in comparison with adjacent normal counterparts. No significant correlation is identified with clinical stages, tumor status, and lymph node status. However, those patients with low KLK11 mRNA expression seem to have a significantly worse prognosis than those with high levels. At the protein level, serum KLK11 concentrations in non-small cell lung cancer patients are higher than in healthy controls and they are positively correlated with tumor stages. |
| Cytogenetics | No cytogenetic abnormalities are identified so far. |
| Hybrid/Mutated Gene | Not identified so far. |
| Breakpoints |
| Note | Not described so far. |
| External links |
| Bibliography |
| A novel isoform of a kallikrein-like protease, TLSP/hippostasin, (PRSS20), is expressed in the human brain and prostate. |
| Mitsui S, Yamada T, Okui A, Kominami K, Uemura H, Yamaguchi N. |
| Biochem Biophys Res Commun 2000; 272: 205-211. |
| PMID 10872828 |
| Alternative splicing isoforms of hippostasin (PRSS20/KLK11) in prostate cancer cell lines. |
| Nakamura T, Mitsui S, Okui A, Kominami K, Nomoto T, Ukimura O, Kawauchi A, Miki T, Yamaguchi N. |
| Prostate 2001; 49: 72-78. |
| PMID 11550212 |
| Human kallikrein 11: a new biomarker of prostate and ovarian carcinoma. |
| Diamandis EP, Okui A, Mitsui S, Luo LY, Soosaipillai A, Grass L, Nakamura T, Howarth DJ, Yamaguchi N. |
| Cancer Res 2002; 62(1): 295-300. |
| PMID 11782391 |
| Favorable prognostic value of tissue human kallikrein 11 (hK11) in patients with ovarian carcinoma. |
| Borgoño CA, Fracchioli S, Yousef GM, Rigault de la Longrais IA, Luo LY, Soosaipillai A, Puopolo M, Grass L, Scorilas A, Diamandis EP, Katsaros D. |
| Int J Cancer 2003; 106: 605-610. |
| PMID 12845660 |
| Molecular cloning and expression of a variant form of hippostasin/KLK11 in prostate. |
| Nakamura T, Mitsui S, Okui A, Miki T, Yamaguchi N. |
| Prostate 2003; 54: 299-305. |
| PMID 12539228 |
| The usefulness of serum human kallikrein 11 for discriminating between prostate cancer and benign prostatic hyperplasia. |
| Nakamura T, Scorilas A, Stephan C, Jung K, Soosaipillai AR, Diamandis EP. |
| Cancer Res 2003; 63: 6543-6546. |
| PMID 14559849 |
| Quantitative analysis of hippostasin/KLK11 gene expression in cancerous and noncancerous prostatic tissues. |
| Nakamura T, Stephan C, Scorilas A, Yousef GM, Jung K, Diamandis EP. |
| Urology 2003; 61: 1042-1046. |
| PMID 12736044 |
| Parallel overexpression of seven kallikrein genes in ovarian cancer. |
| Yousef GM, Polymeris ME, Yacoub GM, Scorilas A, Soosaipillai A, Popalis C, Fracchioli S, Katsaros D, Diamandis EP. |
| Cancer Res 2003; 63: 2223-2227. |
| PMID 12727843 |
| Human kallikrein gene 11 (KLK11) mRNA overexpression is associated with poor prognosis in patients with epithelial ovarian cancer. |
| Shigemasa K, Gu L, Tanimoto H, O'Brien TJ, Ohama K. |
| Clin Cancer Res 2004; 10: 2766-2770. |
| PMID 15102682 |
| Expression analysis and prognostic significance of human kallikrein 11 in prostate cancer. |
| Stavropoulou P, Gregorakis AK, Plebani M, Scorilas A. |
| Clin Chim Acta 2005; 357: 190-195. |
| PMID 15893744 |
| Specificity profiling of seven human tissue kallikreins reveals individual subsite preferences. |
| Debela M, Magdolen V, Schechter N, Valachova M, Lottspeich F, Craik CS, Choe Y, Bode W, Goettig P. |
| J Biol Chem 2006; 281: 25678-25688. |
| PMID 16740631 |
| Inhibition profiles of human tissue kallikreins by serine protease inhibitors. |
| Luo LY, Jiang W. |
| Biol Chem 2006; 387: 813-816. |
| PMID 16800745 |
| Purification and characterization of human kallikrein 11, a candidate prostate and ovarian cancer biomarker, from seminal plasma. |
| Luo LY, Shan SJ, Elliott MB, Soosaipillai A, Diamandis EP. |
| Clin Cancer Res 2006; 12: 742-750. |
| PMID 16467084 |
| Multiple promoters regulate tissue-specific alternative splicing of the human kallikrein gene, KLK11/hippostasin |
| Mitsui S, Nakamura T, Okui A, Kominami K, Uemura H, Yamaguchi N. |
| FEBS J 2006; 273: 3678-3686. |
| PMID 16911518 |
| Expression of the human kallikrein genes 10 (KLK10) and 11 (KLK11) in cancerous and non-cancerous lung tissues. |
| Planque C, Aïnciburu M, Heuzé-Vourc'h N, Régina S, de Monte M, Courty Y. |
| Biol Chem 2006; 387: 783-788. |
| PMID 16800740 |
| Decreased kallikrein 11 messenger RNA expression in lung cancer. |
| Sasaki H, Kawano O, Endo K, Suzuki E, Haneda H, Yukiue H, Kobayashi Y, Yano M, Fujii Y. |
| Clin Lung Cancer 2006; 8: 45-48. |
| PMID 16870045 |
| mRNA expression analysis of human kallikrein 11 (KLK11) may be useful in the discrimination of benign prostatic hyperplasia from prostate cancer after needle prostate biopsy. |
| Scorilas A, Gregorakis AK. |
| Biol Chem 2006; 387: 789-793. |
| PMID 16800741 |
| Improved prostate cancer detection with a human kallikrein 11 and percentage free PSA-based artificial neural network. |
| Stephan C, Meyer HA, Cammann H, Nakamura T, Diamandis EP, Jung K. |
| Biol Chem 2006; 387: 801-805. |
| PMID 16800743 |
| Primary tumor levels of human tissue kallikreins affect surgical success and survival in ovarian cancer patients. |
| Dorn J, Schmitt M, Kates R, Schmalfeldt B, Kiechle M, Scorilas A, Diamandis EP, Harbeck N. |
| Clin Cancer Res 2007; 13: 1742-1748. |
| PMID 17363527 |
| Validation and characterization of human kallikrein 11 as a serum marker for diagnosis of ovarian carcinoma. |
| McIntosh MW, Liu Y, Drescher C, Urban N, Diamandis EP. |
| Clin Cancer Res 2007; 13: 4422-4428. |
| PMID 17671125 |
| Enzymatic properties of human kallikrein-related peptidase 12 (KLK12). |
| Memari N, Jiang W, Diamandis EP, Luo LY. |
| Biol Chem 2007; 388: 427-435. |
| PMID 17391064 |
| Is there a role for serum human tissue kallikrein in detection of prostate cancer? |
| Ochiai A, Shukla A, Davis JW, Fritsche HA, Bhadkamkar V, Babaian RJ. |
| Urology 2007; 70: 519-522. |
| PMID 17905108 |
| Kallikrein 11 expressed in human breast cancer cells releases insulin-like growth factor through degradation of IGFBP-3. |
| Sano A, Sangai T, Maeda H, Nakamura M, Hasebe T, Ochiai A. |
| Int J Oncol 2007; 30: 1493-1498. |
| PMID 17487371 |
| A multiparametric panel for ovarian cancer diagnosis, prognosis, and response to chemotherapy. |
| Zheng Y, Katsaros D, Shan SJ, de la Longrais IR, Porpiglia M, Scorilas A, Kim NW, Wolfert RL, Simon I, Li L, Feng Z, Diamandis EP. |
| Clin Cancer Res 2007; 13: 6984-6992. |
| PMID 18056174 |
| Human kallikrein-related peptidase 14 (KLK14) is a new activator component of the KLK proteolytic cascade. Possible function in seminal plasma and skin. |
| Emami N, Diamandis EP. |
| J Biol Chem 2008; 283: 3031-304. |
| PMID 18056261 |
| A multiparametric serum kallikrein panel for diagnosis of non-small cell lung carcinoma. |
| Planque C, Li L, Zheng Y, Soosaipillai A, Reckamp K, Chia D, Diamandis EP. Goodglick L. |
| Clin Cancer Res 2008; 14: 1355-1362. |
| PMID 18316555 |
| REVIEW articles | automatic search in PubMed |
| Last year publications | automatic search in PubMed |
| Contributor(s) |
| Written | 03-2008 | Liu-Ying Luo, Eleftherios P Diamandis |
| R&D Systems, Inc. 614 McKinley Place, N. E. Minneapolis, MN 55413, USA (LYL); Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, 600 University Ave. Toronto, ON M5G 1X5, Canada (EPD) |
| Citation |
| This paper should be referenced as such : |
| Luo LY, Diamandis EP . KLK11 (Kallikrein-related peptidase 11). Atlas Genet Cytogenet Oncol Haematol. March 2008 . URL : http://AtlasGeneticsOncology.org/Genes/KLK11ID41077ch19q13.html |
| © Atlas of Genetics and Cytogenetics in Oncology and Haematology | indexed on : Sat Feb 6 13:37:52 CET 2010 |
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