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MTA1 of the MTA (metastasis-associated) gene family and its encoded proteins: molecular and regulatory functions and role in human cancer progression

 

Yasushi Toh1, Garth L Nicolson2*

1Department of Gastroenterological Surgery, National Kyushu Cancer Center, Fukuoka, 811-1395, Japan
2Department of Molecular Pathology, The Institute for Molecular Medicine, Huntington Beach, CA 92647, USA

*To whom correspondence and reprint requests should be addressed:
Prof. Garth L. Nicolson, Office of the President,Institute for Molecular Medicine,
P. O. Box 9355, South Laguna Beach, California 92652, USA
Email: gnicolson@immed.org

 

June 2010

 

 

Abstract

MTA1 (a metastasis-associated gene) is a newly discovered human gene (residing on chromsome 14q32.3) that belongs to a family of cancer progression-related genes (MTA). The mRNA product of MTA1 along with its protein product MTA1 have been reported to be over-expressed in a wide variety of animal and human tumors. For example, the expression of MTA1 and its encoded protein MTA1 correlates with the malignant properties of many human cancers, including cancers of the breast, colon, stomach, liver, prostate and others. The MTA proteins have been shown to be ubiquitinated transcriptional co-repressors that function in histone deacetylation and are part of the NuRD complex, a nucleosome remodeling and histone deacetylating complex whose stability appears to be regulated by ubiquitinated MTA1 binding to E3 ubiquitin ligase constitutive photomorphogenesis protein-1 (COP1). The MTA1 protein plays an essential role in c-MYC-mediated cell transformation, and its expression correlates with mammary gland tumor formation. In the latter, MTA1 helps convert mammary cells to more aggressive phenotypes by repression of the estrogen receptor (ER) via trans-activation through deacetylation of chromatin in the ER-responsive element of ER-responsive genes. Another member of the MTA family, MTA3, is induced by estrogen and represses the expression of the transcriptional repressor Snail, a master regulator of epithelial to mesenchymal transformation, resulting in the expression of the cell adhesion molecule E-cadherin and maintenance of a differentiated, normal epithelial phenotype in mammary cells. An important activity mediated by both MTA1 and MTA2 is deacylation and inactivation of tumor suppressor p53 protein, in part by controlling its stability by inhibiting ubiquitination, leading to inhibition of growth arrest and apoptosis. Another factor deacetylated and stabilized by MTA1 NuRD complex is hypoxia-inducible factor-1α (HIF-1α), which is involved in angiogenesis. Therefore, the MTA proteins represent a possible set of master co-regulatory molecules involved in the carcinogenesis and progression of various malignant tumors. As such, they could be important new tools for cancer diagnosis and treatment.

1. Introduction - The MTA gene family

An important advance in cancer research has been the discovery of a wide variety of new molecules involved in carcinogenesis and cancer progression. Although additional cancer-related molecules will be identified in the future, these molecules must fulfill two major requirements in order to be clinically useful as molecular targets useful for the diagnosis and treatment of human cancers (Toh and Nicolson, 2009). The first is that abnormalities must occur in the expression or structure of the molecules of interest, and their clinical relevance must be definitely demonstrated in independent studies on human cancers. The second is that the underlying molecular mechanisms necessary for the molecules to exert their functions in carcinogenesis or cancer progression must be determined and confirmed in animal tumor models and clinical specimens.

There have been a number of cancer-related genes and molecules that have been discovered in the last few years. In our laboratory we identified a candidate metastasis-associated gene by the use of a differential cDNA screening method. Using this approach we identified a gene that was differentially over-expressed in highly metastatic rat mammary adenocarcinoma cell lines compared to poorly metastatic lines (Toh et al., 1994; Toh et al., 1995). When this gene was sequenced, it was shown to be a completely new, novel gene without any homologous or related genes in the database at the time. This gene was named mta1 (metastasis-associated gene-1). A homologous gene was also expressed in human cancer cell lines, and its human cDNA counterpart, MTA1, was subsequently cloned (Nawa et al., 2000) and found to reside on chromosome 14q32.3 (Cui et al., 2001).

Using surgically removed human tissues we showed that high levels of MTA1 mRNA expression were correlated to the invasive and growth properties of gastrointestinal cancers, including esophageal, gastric and colorectal cancers (Toh et al., 1997; Toh et al., 1999). After these studies, several reports from other groups found similar correlations between MTA1 expression and the malignant potentials of human cancers (reviewed in Toh and Nicolson, 2009).

In addition to MTA1, other genes related to MTA1 have now been identified. This gene family, which we termed the MTA family, now has several members plus some splice variants (Toh and Nicolson, 2003; Manavathi and Kumar, 2007; Toh and Nicolson, 2009). Furthermore, studies on the molecular biological and biochemical properties of the MTA family have shown that the gene products of the main members of the family (proteins MTA1, MTA2 and MTA3) are tightly associated in a protein complex called NuRD (nucleosome remodeling and histone deacetylation), which has transcriptional regulatory functions via histone deacetylation and chromatin remodeling (Toh et al., 2000; Bowen et al., 2004). Interestingly, histone deacetylase activities correlate with squamous cell carcinoma invasion (Toh et al., 2003). At the moment, the MTA family has attracted widespread attention as one of several key molecules that play indispensable roles in the pathogenesis and progression of a wide variety of cancers (Toh and Nicolson, 2003; Kumar et al., 2003; Manavathi et al., 2007b; Toh and Nicolson, 2009). We will examine the significance of the expression of MTA family members in human cancers and the important molecular mechanisms that are currently known by which MTA proteins exert their cellular actions as well as discuss the potential clinical applications of this protein family for the diagnosis and treatment of human cancers.

2. The MTA family of proteins, their structures and cell location

The MTA proteins represent a family of gene products encoded by three distinct genes (MTA1, MTA2 and MTA3), and six reported isoforms (MTA1, MTA1s, MTA1-ZG29p, MTA2, MTA3, and MTA3L). The molecular masses of the gene products of MTA1, MTA2 and MTA3 are approximately 80 kDa, 70 kDa and 65 kDa, respectively (Manavathi and Kumar, 2007; Toh and Nicolson, 2009). The nucleotide and protein alignment homologies and the phylogenetic comparative analyses have been discussed previously (Bowen et al., 2004; Manavathi and Kumar, 2007; Toh and Nicolson, 2009).

The MTA gene family sequences, with the exception of ZG-29p, contain several common domain structures (Singh and Kumar, 2007; Toh and Nicolson, 2009). One of these, the BAH (bromo-adjacent homology) domain is involved in protein-protein interactions. Another, the SANT (SWI, ADA2, N-CoR, TFIIIB-B) domain shares a high degree of homology with the DNA-binding domain of the Myb-related proteins, suggesting that this domain may be involved in DNA-binding. The ELM (egl-27 and MTA1 homology) domain has an unknown function but could be involved in embryonic patterning (Solari et al., 1999).

The MTA family members contain a highly conserved GATA-type zinc finger motif, suggesting direct interactions with DNA (Nawa et al., 2000). The MTA1 protein has two src-homology (SH)-binding motifs at its C-terminal end-such binding domains are known to be important in signal transduction involving kinase, adaptor and scaffolding proteins (Toh et al., 1994; Toh et al., 1995; Singh and Kumar, 2007). Similarly, SH2- and SH3-binding domains are also found in MTA2 and MTA3 protein sequences (Toh et al., 1994; Toh et al., 1995; Singh and Kumar, 2007). These common domain structures demonstrate that the MTA family is involved in protein-protein and protein-DNA interactions, indicating the anticipated roles of the MTA family of proteins in signal transduction and transcriptional regulation (Toh and Nicolson, 2003; Singh and Kumar, 2007; Toh and Nicolson, 2009).

In addition to protein-protein and protein-DNA binding, MTA proteins contain basic nuclear localization signals (Toh et al., 1994; Toh et al., 1995; Singh and Kumar, 2007). They also localize in the nucleus in many human cancer cells (Toh et al.,1997; Toh et al., 1999); however, MTA1 localizes to both the cytoplasm and nucleus in some tumors (Moon et al., 2004; Balasenthil et al., 2006; Bagheri-Yarmand et al., 2007). MTA3 also localizes to the nucleus, but without any apparent nuclear localization signal (Fujita et al., 2003). A short splice-variant of MTA1, called MTA1s, is predominantly localized in the cytoplasm (Kumar et al., 2002).

3. MTA protein expression in various cancers and its possible clinical relevance

Since the report by Toh et al. (1997) that the over-expression of MTA1 was significantly correlated to the malignant properties of human gastric and colorectal cancers, there have been several reports on the expression levels of MTA family members, especially of MTA1, in various human cancers (reviewed in Toh and Nicolson, 2009). These studies revealed that the expression levels of MTA family members correlate with pathogenic significance and prognosis (Toh and Nicolson, 2009). The biological relevance of MTA proteins to carcinogenesis and cancer progression has been investigated in a few cancer models, such as breast and gastrointestinal cancers, and these will be discussed in more detail below.

3.1 MTA1 protein and breast cancer

MTA1 protein was originally identified as a candidate cancer progression molecule that was associated with breast cancer metastasis (Toh et al., 1994; Toh et al., 1995). Subsequently, using antisense RNA of MTA1 a role for MTA1 in the growth properties of metastatic breast cancer cells was investigated. Using MTA1 antisense RNA we found that the growth rates of highly metastatic breast cancer cell lines were inhibited significantly in a dose-dependent manner (Nawa et al., 2000). More direct evidence to demonstrate an association of MTA1 expression levels with breast cancer malignant properties was obtained by Mazumdar et al. (2001). They demonstrated that forced expression of the MTA1 protein in the human breast cancer cell line MCF-7 was accompanied by an enhancement in the ability of MCF-7 cells to invade an artificial matrix and ability to grow in an anchorage-independent manner. They also showed that the enhancement was associated with the interaction between MTA1 protein and histone deacetylase, resulting in a repression of estrogen receptor (ER) mediated transcription (Mazumdar et al., 2001).

Using an animal model the Mazumdar et al. (2001) study was extended by further experiments demonstrating a direct in vivo effect of MTA1 on the carcinogenesis of breast cancer cells (Bagheri-Yarmand et al., 2004; Singh and Kumar, 2007). This group established a transgenic mice system that over-expressed the MTA1 protein, and these MTA1-transgenic mice revealed inappropriate development of their mammary glands. The MTA1-transgenic mice eventually developed hyperplastic nodules and mammary tumors, including mammary adenocarcinomas and lymphomas.

The involvement of MTA1 in the carcinogenesis and progression of breast cancers was also shown by Martin et al. (2001; 2006). First, they mapped the chromosomal locus in 14q that might be responsible for axillary lymph node metastases in human breast cancers by comparing the rate of loss of heterozygosity between node-positive and node-negative breast cancers. The MTA1 gene was found to be contained in the same gene locus, suggesting that MTA1 is a candidate for a breast cancer metastasis-promoting gene. Next, using immunohistochemistry they examined MTA1 protein expression in primary human breast cancer samples and demonstrated that node-negative breast cancers with over-expression of MTA1 protein had a higher risk of disease relapse similar to node-positive tumors. Therefore, the over-expression of MTA1 was proposed as a potential predictor of early disease relapse independent of node status (Martin et al,. 2006).

Using surgically resected human breast cancer specimens Jang et al. (2006) showed that MTA1 over-expression was closely associated with higher tumor grade and high intratumoral microvessel density. This suggested that MTA1 could be a useful predictor of an aggressive phenotype, and the MTA1 molecule could be considered as a possible angiogenesis-promoting molecule in breast cancers (Jang et al., 2006).

3.2 MTA1 protein and gastrointestinal cancers

MTA1 over-expression has been shown to be pathogenically significant in human gastrointestinal cancers. Using a reverse-transcription polymerase chain reaction (RT-PCR) method on surgically resected human gastric and colorectal cancer specimens were compared to paired normal counterpart tissues, and we found that the higher expression of MTA1 mRNA was significantly correlated to the depth of cancer invasion and extent of lymph node metastasis (Toh et al., 1997). This study was the first to demonstrate the clinical relevance of MTA1 expression to the malignant potentials of human cancers. Over-expression of MTA1 mRNA was also shown in colorectal cancers compared to the normal counterpart tissues (Giannini et al., 2005).

Esophageal cancers have also been investigated for MTA1/MTA1 over-expression. Using a RT-PCR method we found that human esophageal squamous cell cancers over-express MTA1 mRNA (Toh et al., 1999). The over-expressing cancer cells showed significantly higher frequencies of adventitial invasion and lymph node metastasis and tended to have higher rates of lymphatic involvement (Toh et al., 1999). Using immunohistochemistry we further examined the expression levels of MTA1 protein in human esophageal squamous cell cancers and reconfirmed the results obtained by RT-PCR (Toh et al., 2004). In the same study we also demonstrated that MTA1 protein was a predictor of poor prognosis after surgery (Toh et al., 2004).

The roles of MTA1/MTA1 in small intestinal cancers have also been evaluated. Kidd et al. (2006a; 2007) and Modlin et al. (2006b) showed that it was useful to examine the expression of MTA1 mRNA and MTA1 protein in order to determine the malignant potential and the propensity to metastasize of enterochromaffin cell cancers (small intestinal carcinoid tumors). When compared to nonmetastatic primary tumors, the expression of MTA1 was increased in malignant, invasive small intestinal carcinoid tumors and in metastases to liver and lymph nodes. In these cells loss of TGFβ expression modified expression, including increased MTA1 expression, of the genes involved in malignant behavior (Kidd et al., 2007). It was further reported that MTA1 was a good candidate genetic molecular marker to discriminate between gastric carcinoids and other gastric neoplasms (Kidd et al., 2006b) as well as malignant appendiceal carcinoids from benign tissue (Modlin et al., 2006a). In these studies, MTA1 and MTA1 expression were thought to be good markers of the malignant potential of carcinoid tumors.

Other gastrointestinal-linked cancers, such as a pancreatic cancers and hepatocellular carcinomas, have also been examined for the involvement of MTA1/MTA1 over-expression in carcinogenesis and cancer progression. Iguchi et al. (2000) examined MTA1 mRNA expression in pancreatic cancer cell lines and resected pancreatic cancer tissues and found that increased levels of MTA1 mRNA expression in the more progressed pancreatic cancers. Direct evidence on the role of MTA1/MTA1 in the progression of pancreatic cancer was provided by Hofer et al. (2004). Using a pancreatic cell line (PANC-1) they transfected MTA1 cDNA into the cells and found that enhanced expression of MTA1 promoted the acquisition of an invasive and metastatic phenotype and enhanced the malignant potentials of the transformed cells (pancreatic adenocarcinomas) by modulation of the cytoskeleton via IQGAP1. In addition, Miyake et al. (2008) showed the expression level of the MTA1 protein correlated with poorer prognosis of pancreatic cancer patients.

An association between MTA1/MTA1 expression and the malignant properties of hepatocellular carcinomas (HCC) was first reported by Hamatsu et al. (2003). In this study, MTA1 mRNA level was assessed by RT-PCR in resected human HCC tissues, and its high expression predicted a lower disease-free survival rate after curative HCC hepatectomy. Using immunohistochemistry Moon et al. (2004) examined MTA1 protein expression in resected human HCC specimens and found that over-expression of MTA1 was associated with HCC growth and vascular invasion and that nuclear localization of ERa inversely correlated with MTA1 expression. This suggested that MTA1 was involved in negative regulatory mechanisms.

Recently, Yoo et al. (2008) demonstrated that hepatitis B virus (HBV) X (HBx) protein strongly induced the expression of MTA1 and histone deacetylase 1 (HDAC1). This suggests that positive crosstalk between HBx and MTA1/HDAC1 complex may occur, and this could be important in stabilizing hypoxia-inducible factor-1α (HIF1-1α), which appears to play a critical role in angiogenesis and metastasis of HBV-associated HCC (Yoo et al., 2008). Interestingly, it was reported that MTA1 was closely associated with microvascular invasion, frequent postoperative recurrence, and poor prognosis in patients with HCC, especially in those with HBV-associated HCC (Ryu et al., 2008).

3.3 MTA1 protein and other cancers

The reports on MTA1/MTA1 over-expression in human cancers have been reinforced by the experimental over-expression or under-expression of MTA1 in human cells. For example, Mahoney et al. (2002) transfected MTA1 cDNA into immortalized human keratinocytes and demonstrated that forced over-expression of MTA1 contributed to some metastatic cell properties, such as increased cell migration, invasion and survival in an anchorage independent medium. Nawa et al. (2000) used antisense MTA1 to suppress MTA1 levels and inhibit the growth of breast cancer cells in vitro. These authors subsequently showed that in vitro invasion of human MBA-MB-231 cells could be inhibited by antisense MTA1 (Nicolson et al., 2003). Similarly, using a human esophageal squamous cell carcinoma cell line, Qian et al. (2005) inhibited MTA1 expression by RNA interference and found significant inhibition of the cells' in vitro invasion and migration properties.

Possible relationships between MTA1/MTA1 expression and malignant cell properties, such as invasion and metastasis, have been investigated in other carcinoma and sarcoma systems. Using human non-small cell lung cancer cells high expression of MTA1 mRNA was correlated with lymph node metastasis (Sasaki et al., 2002). This has also been found to be the case in human ovarian cancers (Yi et al., 2003). Additionally, in thymomas advanced stage and invasiveness was related to MTA1 expression (Sasaki et al., 2001).

Using various techniques the relationship between MTA1 expression and malignancy has been investigated in various cancers. For example, a potential role for MTA1 protein over-expression in the progression of human endometrial carcinomas has been found by Balasenthil et al. (2006). Whereas in prostate cancers Hofer et al. (2004) showed that metastatic prostate tumors had significantly higher levels of MTA1 protein expression and higher percentages of tissue cores staining positive for MTA1 protein over-expression than in clinically localized prostate cancers or benign prostate lesions. Most interestingly, using transgenic mice Kumar's group showed that MTA1 over-expression was accompanied by a high incidence of spontaneous B cell lymphomas, including diffuse large B cell lymphomas (Bagheri-Yarmand et al., 2007; Balasenthil et al., 2007). The high expression of MTA1 in human diffuse B-cell lymphomas has been reported (Hofer et al., 2006). In the transgene model, mammary adenocarcinomas also developed (Bagheri-Yarmand et al., 2004).

Microarrays have also been used to follow MTA1 and other genes' expression. Using DNA microarray analysis Roepman et al. (2006) investigated gene expression patterns in lymph node metastases of head and neck squamous cell carcinomas. They found that the MTA1 gene was the only single gene that showed consistent over-expression between large numbers of matched paired samples of primary tumor and lymph node metastases.

4. Biological significance of the MTA proteins

It has been demonstrated by different laboratories (see Section 3) that MTA1/MTA1 over-expression is closely correlated with cancer progression (and in some cases with carcinogenesis) in a wide range of different cancers. This strongly indicates that the MTA1 protein may be an important functional molecule in malignancy. Thus, it is necessary to clarify the molecular mechanisms by which the MTA protein family members exert their functions. Only then can MTA proteins be utilized for diagnosis or treatment of human cancers. There are several important cellular functions of MTA proteins that have been recently clarified, such as those that are related to carcinogenesis and cancer progression.

4.1 MTA proteins and the nucleosome remodeling-histone deacetylation (NuRD) complex and transcriptional regulation

The molecular and biochemical functions of the MTA1 protein were first investigated by four independent groups. In these studies, two different chromatin-modifying activities, ATP-dependent nucleosome remodeling activity and histone deacetylation, were functionally and physically linked in the same protein complex. This complex has been named the NuRD (Nucleosome Remodeling and Histone Deacetylation). The NuRD complex contains HDAC1, HDAC2, the histone binding proteins RbAp46/48 and the dermatomyositis-specific autoantigen Mi-2, which has been shown to have transcription repressing activity (Tong et al., 1998; Xue et al., 1998; Wade et al., 1999; Zhang et al., 1999; Bowen et al., 2004).

The MTA1 protein was found in the NuRD complex by Xue et al. (1998), and this complex also possessed strong transcription repressing activity. Subsequently, Zhang et al. (1999) reported that a protein similar to MTA1 (named the MTA2 protein) was also a component of the NuRD complex, and they found that MTA2 protein was highly expressed in rapidly dividing cells. Later, MTA3 protein was identified as an estrogen-inducible gene product that is present in a distinct NuRD complex (Fujita et al., 2003). We also reported the physical interaction between MTA1 protein and HDAC1 (Toh et al., 2000).

The basic functions of the MTA protein family members appear to be exerted through NuRD complexes as chromatin remodeling and histone deacetylating activities (Figure 1). Although there are also non-histone deacetylating proteins in NuRD complexes, MTA proteins appear to be among the principal components (Figure 1). In addition, the MTA-NuRD complexes show transcriptional repression activities (Feron, 2003; Kumar et al., 2003; Manavathi et al., 2007b; Singh and Kumar, 2007). Although all MTA protein family members are found in NuRD complexes, each MTA protein may form a distinct NuRD complex that targets different sets of promoters (Bowen et al., 2004).

Figure 1. MTA proteins in a chromatin remodeling and histone deacetylation complex (NuRD). This complex has transcription repression properties. The NuRD complex also contains histone deacetylases (HDAC1 and 2), major DNA binding protein 3 (MDB3), histone binding proteins RbAp46/48 and the dermatomyositis-specific autoantigen Mi-2 (from Toh and Nicolson, 2009 with permission).

4.2 MTA protein repression of the trans-activating activity of estrogen receptor-alpha

The involvement of MTA proteins in NuRD complexes suggested that such complexes might function in chromatin remodeling and histone deacetylation, but a direct target of a MTA protein had to first be identified (Mazumdar et al., 2001). MTA1 protein was identified as a molecule induced by heregulin-beta1 (HRG), a growth factor that is a natural ligand of the human epidermal growth factor receptors HER3 and HER4. It can also trans-activate HER2 (c-erbB-2) in human breast cancer cell lines. Mazumdar et al. (2001) showed that MTA1 protein directly interacted with the ligand-binding domain of the estrogen receptor ERα and that HRG stimulated the association of MTA1 and HDAC2 on the chromatin site of an ER-responsive element (ERE) in the promoter regions of estrogen responsive genes, such as pS2 and c-myc. This could explain the activation of the HRG/HER2 pathway in ER-positive breast cancers and the suppression of ERα functions, which could result in the more invasive and aggressive phenotypes observed in ER-negative breast cancers (Cui et al., 2006).

The repressive function of MTA1 protein on ERα is mediated via histone deacetylation by HDAC1 and HDAC2, suggesting that MTA1 protien has a potent co-repressor function during the trans-activation of ERα through histone deacetylation (Figures 2 and 3). MTA2 protein has also been shown to physically interact with ERα and to repress its trans-activating function. This could explain the over-expression of MTA2 protein in cells that were unresponsive to estrogen as well as suppression of estrogen-induced colony formation in breast cancer cells (Cui et al., 2006).

Figure 2. A possible role for MTA proteins in carcinogenesis and cancer progression. In this scheme the main functions of the MTA family of proteins are presented. (A) MTA1 protein is included in a NuRD complex that represses the transactivation function of estrogen receptor (ER), rendering breast cancer cells more phenotypically aggressive. MTA1 proteins in NuRD complexes are proposed to be one of the first downstream targets of c-MYC function, and it is essential for the transformation potential of c-MYC. MTA1s is a splice-variant of MTA1 that localizes in the cytoplasm where it sequesters ERα, preventing the ligand-induced nuclear translocation of Erα, thus stimulating the development of the malignant phenotype of breast cancer cells. (B) MTA3 protein induced by estrogen represses the expression of the transcriptional repressor Snail, a master regulator of epithelial to mesenchymal transitions, resulting in the expression of the cell adhesion molecule E-cadherin and maintenance of a differentiated, normal epithelial status in breast cells (from Toh and Nicolson, 2009 with permission).

MTA proteins also have other activities. For example, Khaleque et al. (2008) showed that MTA1 protien binds to a heat shock factor 1 (HSF1), the transcriptional activator of the heat shock genes, in vitro and in human breast carcinoma samples. They demonstrated that HSF1-MTA1 complex formation was strongly induced by HRG and that the complex was incorporated into a NuRD complex that participated in the repression of estrogen-dependent transcription in breast cancer cells treated with HRG (Khaleque et al., 2008).

There are apparently several molecules, such as ménage-à-trois 1 (MAT1), MTA1-interacting co-activator (MICoA) and nuclear receptor interacting factor 3 (NRIF3), that can interact with MTA1 protein and repress the trans-activation function of ERα (Manavathi et al., 2007b). These three MTA1-binding proteins themselves have co-activator properties upon ERα trans-activation. MAT1, an assembly and targeting ring finger factor for cyclin-dependent kinase-activating kinase (CAK), has been identified by Talukder et al. (2003) as a MTA1-binding protein. The interactions between CAK and MTA1 protein apparently regulate the trans-activation activity of ERα in a CAK-dependent manner in breast cancer cells. In contrast, MICoA-mediated ERα trans-activation functions are opposed by MTA1 protein through the recruitment of HDACs (Mishra et al., 2003). In addition, the interactions between MTA1 protein and NRIF3 (an estrogen-inducible gene) may be important in modulating the sensitivity of breast cancer cells to estrogen (Talukder et al., 2004).

Another MTA1-binding protein partner, Lim-only protein 4 (LMO4), has been identified by Singh et al. (2005). LMO4 was found to be a component of the MTA1 co-repressor complex, and its over-expression repressed ERα trans-activation in a HDAC-dependent manner. This has been proposed to result in the acquisition of an ERα-negative phenotype with its known increased aggressiveness in breast cancer cells (Singh et al., 2005).

Variants of MTA1 protein have also been found. For example, a truncated form of MTA1 protein has been identified and named MTA1s (Balasenthil et al., 2006). MTA1s is a splice-variant of MTA1, and it contains an ER-binding motif (nuclear binding motif) without any nuclear localization signals at its C-terminus. This truncated MTA protein localizes in the cytoplasm where it sequesters ERα, resulting in the blockage of ERα ligand-induced nuclear translocation and stimulation of acquisition of the malignant phenotype of breast cancer cells. This suggests that the regulation of the cellular localization of ERα by MTA1s protein may represent a mechanism for redirecting nuclear receptor signaling by nuclear exclusion. MTA1s protein has also been shown to associate with casein kinase I-gamma2, which is an estrogen-responsive kinase (Mishra et al., 2004).

MTA3 protein is the newest addition to the MTA family. It was identified as an estrogen-dependent component of the Mi-2/NuRD transcriptional co-repressor complex in breast epithelial cells (Fujita et al., 2003). The absence of MTA3 protein as well as the absence of ER results in an aberrantly increased expression of the transcriptional repressor Snail, a master regulator of epithelial-to-mesenchymal transition (EMT). This increased expression of Snail results in reduction in expression of the cell adhesion molecule E-cadherin, which subsequently modifies epithelial cell architecture and enhances invasive growth. MTA3 protein is a transcriptional target of ERα, and in the presence of estrogen ERα directly binds to the MTA3 promoter at the SP1 site in close proximity to the ERE half-site, resulting in stimulation of MTA3 transcription (Fujita et al., 2004; Mishra et al., 2004). Thus, MTA3 protein may function to maintain a well-differentiated, normal epithelial phenotype in breast cells. This is in stark contrast to MTA1 or MTA1s protein, where up-regulation of MTA1 or MTA1s protein in breast cancer cells may repress MTA3 expression through repression of the ERα function, resulting in up-regulation of Snail, down-regulation of E-cadherin, promotion of an EMT phenotype and potentially an increase in metastatic potential.

Forced expression of MTA3 protein inhibits ductal branching in virgin and pregnant mammary glands in MTA3-transgenic mice (Zhang et al., 2006). This property is in marked contrast to MTA1-transgenic mice, where there is inappropriate development of mammary glands, resulting in the development of hyperplastic nodules and mammary tumors, including adenocarcinomas and lymphomas (Bagheri-Yarmand et al., 2004; Manavathi and Kumar, 2007). MTA3 protein also represses Wnt4 transcription and secretion by inhibiting Wnt-target genes in mammary epithelial cells. This repression of Wnt4 transcription was found to be mediated through a MTA3-NuRD complex, which interacts with the Wnt4-containing chromatin in an HDAC-dependent process (Zhang et al., 2006).

The fundamental actions of the MTA proteins are exerted via transcriptional repression by histone deacetylation; however, a transcriptional activating function has also been described for MTA complexes. Gururaj et al. (2006a, 2006b) showed that breast cancer amplified sequence 3 (BCAS3), a gene amplified and over-expressed in breast cancers, was a chromatin target of MTA1 protein, and the transcription of BCAS3 was stimulated by MTA1 protein. This suggested that MTA1 protein has a transcriptional co-activator function in addition to its co-repressor function. A similar property has been also been suggested for mouse Mta2 protein (Matsusue et al., 2001).

Figure 3. Deacetylation of non-histone proteins by MTA protein family complexes. (A) Tumor suppressor p53 protein is deacetylated and inactivated by both MTA1 and MTA2 proteins in NuRD complexes, resulting in inhibition of growth arrest and apoptosis. (B) Hypoxiainducible factor-1α (HIF-1α) is also deacetylated and stabilized by MTA1 protein, leading to angiogenesis (from Toh and Nicolson, 2009 with permission).

4.3 MTA-NuRD protein complexes and deacetylation of non-histone proteins

Chromatin histones and non-histone proteins are the protein targets for deacetylation by HDAC via NuRD complexes containing MTA proteins. The tumor suppressor gene p53 protein was the first non-histone protein that was reported to be deacetylated by MTA protein-containing NuRD complexes. Luo et al. (2000) reported that the deacetylation of p53 was mediated by an HDAC1 complex containing MTA2 protein. A MTA2-associated NuRD complex was involved, and this HDAC1/MTA2 complex interacted with p53 in vitro and in vivo and reduced significantly the steady-state levels of acetylated p53. Deacetylation of p53 causes an increase in its own degradation through MDM2 and a reduction in p53-dependent transcriptional activation. Eventually this results the repression of the normal p53 function that mediates cell growth arrest and apoptosis (Figure 3). The same phenomenon was observed between p53 and MTA1 complexes. HDAC1/MTA1 complexes possessed deacetylation activity against p53 protein in human non-small cell carcinoma and human hepatoma cells, and the complexes were found to inhibit p53-induced apoptosis by attenuating the trans-activation function of p53 (Moon et al., 2007). More recently the stability of p53 was determined to be affected by MTA1 inhibiting p53 ubiquitination by E3 ubiquitin ligases double minute 2 (Mdm2) and constitutive photomorphogenic protein 1 (COP1). MTA1 competes with COP1 to bind to p53 and/or destabilize COP1 and Mdm2 (Li et al., 2009b). MTA1 stability and degradation itself is controlled by ubiquitination, and degradation of MTA1 is promoted by COP1-mediated hydrolysis (Li et al., 2009b).

HIF-1α (hypoxia-inducible factor-1α) is another important non-histone protein that is deacetylated by HDAC1/MTA1 complexes (Figure 3). HIF-1α is a key regulator of angiogenic factors (Yoo et al., 2006). The expression of MTA1 was strongly induced under hypoxic conditions in breast cancer cell lines, and MTA1 protein over-expression enhanced the transcriptional activity and stability of HIF-1α protein. MTA1 protein physically bound to HIF-1α and deacetylated it by increasing the expression of HDAC1, leading to the stabilization of HIF-1α (Yoo et al., 2006). These results indicated possible positive cross-talk between MTA1 and HIF-1α, mediated by HDAC1 recruitment.

Moon et al. (2006) found a close connection between MTA1-associated metastasis and HIF-1α-induced tumor angiogenesis. They showed that MTA1 protein increased the transcriptional activity of HIF-1α and a target molecule of HIF-1α, vascular endothelial growth factor (VEGF). Conditioned medium collected from MTA1-transfectants increased angiogenesis in vitro and in vivo (Moon et al., 2006). Functional links between HIF-1α and MTA1 protein have been demonstrated in clinical samples of pancreatic carcinoma. Using immunohistochemistry and surgically resected pancreatic carcinomas Miyake et al. (2008) examined the expression of HIF-1α, HDAC1 and MTA1 proteins and suggested that HIF-1α expression, which is associated with a poor prognosis in patients with pancreatic cancers, might be regulated by HDAC1/MTA1 complexes. The contribution of MTA1 protein to tumor angiogenesis was also demonstrated in human breast cancers. Using immunohistochemistry Jang et al. (2006) examined MTA1 protein expression and intra-tumoral microvessel density (MVD) in clinical samples of breast cancer and showed that MTA1 protein expression was significantly correlated with higher tumor grade and higher tumor MVD.

The relationship between MTA1 protein expression and MVD was also observed in hepatitis B-associated HCC (Ryu et al., 2008). In this tumor system hepatitis B virus X protein (Hbx) induces the expression of MTA1 protein and its HDAC1 complex, which enhances hypoxia signaling in HCC (Yoo et al., 2006). This suggests that the HDAC1 complex containing MTA1 protein may be important in stabilizing HIF-1α, and thus play a role in angiogenesis and metastasis.

The relationship between the protein members of NuRD complexes, including MTA1 and MTA2 proteins, and the ataxia teleangiectasia mutated (ATM)- and Rad3-related protein (ATR) has been shown by co-immunoprocipitation of these proteins (Schmidt and Schreiber, 1999). ATR is a phosphatidylinositol-kinase-related kinase that has been implicated in the response of human cells to multiple forms of DNA damage and may play a role in the DNA replication checkpoint. This suggests that MTA proteins may contribute to the regulation of DNA checkpoints (Toh and Nicolson, 2009).

4.4 MTA proteins: other possible functions in cancer cells

Other reports have been forthcoming suggesting some possible roles of MTA proteins in carcinogenesis and cancer progression. The most important of these may be the relationship of MTA1 protein with c-MYC oncoprotein (Figure 2). Using expression profiling, Zhang et al. (2005) identified the MTA1 protein as a target of the c-MYC protein in primary human cancer cells. They showed that c-MYC binds to the genomic MTA1 locus and recruits transcriptional co-activators. They also found that the MTA1 proteins in NuRD complexes were one of the first downstream targets of c-MYC function, and this was essential for the transformation potential of c-MYC. Indeed, reduction of MTA1 expression by a short hairpin RNA blocked the ability of c-MYC to transform mammalian cells (Zhang et al., 2005).

Another milestone was the establishment of a transgenic mice model that over-expressed MTA1 protein. Kumar and his collaborators found that the MTA1-transgenic mice showed inappropriate development of mammary glands. These mice also developed hyperplastic nodules and mammary tumors (Bagheri-Yarmand et al., 2004; Singh and Kumar, 2007). In this study, the underlying molecular mechanisms of MTA1 protein action and its regulation were also examined, and the results suggested that MTA1 protein dysregulation in mammary epithelium and cancer cells triggered down-regulation of the progesterone receptor-B isoform and up-regulation of the progesterone receptor-A isoform, resulting in the up-regulation of the progesterone receptor-A target genes Bcl-XL and cyclin D1 in mammary glands of virgin mice. These authors also found that spontaneous B-cell lymphomas were induced in the MTA1-transgenic mice (Bagheri-Yarmand et al., 2007).

Recently, Molli et al. (2008) reported that MTA1/NuRD complexes negatively regulated BRCA1 transcription by physically associating with ERE of the BRCA1 promoter in an ERα-dependent manner. This repressive effect of MTA1 on BRCA1 expression resulted in the acquisition of abnormal centrosomes and chromosomal instability (Molli et al., 2008).

The expression of MTA1 and HDAC1 proteins can also be increased by the interaction of hepatitis B virus X (HBx) protein at the transcriptional level (Yoo et al., 2008). Since MTA1 and HDAC1/2 proteins are physically associated with HIF-1α in vivo in the presence of HBx protein, HBx-induced deacetylation stabilizes HIF-1α by inhibiting proteosomal degradation. These results indicated the existence of positive cross-talk between HBx and the MTA1/HDAC complex, and it further suggests that such cross-talk may play a role in angiogenesis and metastasis of HBV-associated hepatocellular carcinomas.

Direct interactions between MTA1 protein and endophilin 3 have also been reported by Aramaki et al. (2005). This suggests that MTA1 protein might be involved in the regulation of endocytosis mediated by endophilin 3.

An important treatment modality in cancer is the use of ionizing radiation. MTA1 protein has been implicated in ionizing radiation-induced DNA damage response by regulating p53-dependent DNA repair (Li et al., 2009a).

5. MTA/MTA genes and proteins as new clinical targets

This review and others (Nicolson et al., 2003; Manavathi and Kumar, 2007; Toh and Nicolson, 2009) have discussed the available data on the likelyhood that MTA proteins have important and critical roles in the genesis and progression of a wide variety of cancers. MTA1 protein can be thought of as a master co-regulatory molecule (Manavathi and Kumar, 2007; Toh and Nicolson, 2009). This clearly suggests the possibility that MTA1 protein (or the MTA1 gene or its RNA product) could be an excellent molecular target for cancer therapy as well as its use in cancer diagnosis/prognosis.

The first studies that suggested the possibility of targeting MTA1 RNA were reported by Nawa et al. (2000) and Nicolson et al. (2003). Using antisense phosphorothioate oligonucleotides against MTA1 mRNA, these authors found growth inhibitory effects and inhibition of invasion of human metastatic breast cancer cell lines.

Different techniques have been used to regulate MTA1/MTA1 expression in order to determine the effects of MTA1 protein on cellular functions. Using RNA interference (RNAi) Qian et al. (2007) inhibited MTA1 expression in a human esophageal squamous cell carcinoma cell line and demonstrated significant inhibition of in vitro invasion and migration properties of the cancer cells (Qian et al., 2005). In a metastasis model based on murine melanoma Qian et al. (2007) examined the therapeutic use of lowering MTA1 protein levels in the melanoma cells and demonstrated that down-regulation of MTA1 protein by RNAi successfully suppressed growth in vitro and experimental metastasis in vivo. Using microRNAs against MTA1 Reddy et al. (2009) were able to inhibit the expression of MTA1 protein in human breast cancer cells, resulting in decreased cell mobility, invasiveness, anchorage-dependent growth and tumorigenicity. Results such as these suggest a potential role of the MTA1 gene as a target for cancer gene therapy.

Other MTA/MTA genes and proteins may also be useful targets. For example, MTA1s may be a useful target in the treatment of breast cancer. MTA1s functions as a repressor of ERα transcriptional activity by binding and sequestering the ERα in the cytoplasm (Kumar et al., 2002). MTA1s has a unique C-terminal 33-amino acid region containing a nuclear receptor-box motif that mediates the interaction of MTA1s protein with ERα. Singh et al. (2006) showed that the MTA1s peptide containing this motif could effectively repress the ERα transactivation function, measured by estrogen-induced proliferation and anchorage-independent growth of the human breast cancer cell line MCF-7. Using an animal model they also showed the effect of MTA1s peptide in blocking tumor progression of MCF-7 breast cancer cells that over-expressed ERα (Singh et al., 2006).

The use of MTA1 protein as a target of immunotherapy has also been considered. MTA1 protein is a promising antigen for tumor rejection, because it is over-expressed in many different tumors and is only expressed at lower levels in normal tissues (Toh and Nicolson, 2009). In reviewing a model for immunotherapy Assudani et al. (2006) proposed using a vector that contained disabled infectious single cycle-herpes simplex virus (DISC-HSV). Their initial studies demonstrated the presence of immunogenic MHC class I-restricted peptides of MTA1 protein. Next, MTA1 protein was identified as a SEREX antigen, and hence it is likely to be capable of inducing a T-cell response in cancer patients (Chen and Han, 2001).

6. MTA/MTA genes and proteins: future directions

This and previous reviews (Toh and Nicolson, 2003; Manavathi and Kumar, 2007; Toh and Nicolson, 2009) have focused on the clinical and biological significance of the newly emerging gene family named MTA. The family of MTA proteins is made up of transcriptional co-repressors that function via NuRD complexes containing chromatin remodeling and histone deacetylating molecules. These actions clearly have a role in tumor formation and progression. For example, the repression of ERα trans-activation function by MTA1 protein through deacetylation of ERE chromatin of the ER-responsive genes has been the most extensively investigated, and the data clearly demonstrated that MTA1 expression results in tumor formation in mammary glands and renders breast cancer cells phenotypically more aggressive (reviewed in Manavathi and Kumar, 2007).

In addition to chromatin histones, MTA proteins also deacetylate non-histone proteins. For example, the tumor suppressor p53 protein is deacetylated and inactivated by both MTA1 and MTA2 proteins, resulting in inhibition of growth arrest and apoptosis. HIF-1α is also deacetylated and stabilized by MTA1, leading to angiogenesis. Thus, it has been proposed that MTA proteins, especially MTA1 protein, represent master co-regulatory molecules involved in the carcinogenesis and progression of various malignant tumors (Manavathi and Kumar, 2007; Toh and Nicolson, 2009). Since, it is assumed that these properties are important to the survival and progression of cancer cells, ultimately this could lead to novel clinical applications of MTA genes or MTA proteins as new molecular targets for cancer therapy.

There are other examples of the potential use of MTA proteins as therapeutic targets. Inhibition of MTA1 protein expression or function may enhance the chemosensitivity of cancer cells by restoring tumor suppressor function of p53, or it may inhibit tumor angiogenesis by destabilizing the angiogenesis promoting function of HIF-1α. Moreover, MTA proteins may cooperate with HDAC inhibitors, which are now expected to be the target of a new class of anticancer agents (Toh and Nicolson, 2009).

MTA1 will also be clinically useful for the prognosis or prediction of the malignant potentials of various human cancers, such as esophageal, gastric and colorectal cancers (Toh and Nicolson, 2009). Thus, evaluating the expression levels of MTA proteins in individual cases of various cancers may provide us with important clues.

Finally, the MTA proteins are clearly present in completely normal cells to provide them with certain necessary functions. Thus, it will be important to understand their physiological functions and underlying mechanisms in normal cells. For example, C. elegans has MTA1 homologues, egl-27 and egr-1, that function in embryonic patterning and development (Solari et al., 1999; Chen and Han, 2001), suggesting that MTA1 protein may have an embryonic developmental function. MTA1 protein is also thought to play a crucial role in postnatal testis development and spermatogenesis (Li et al., 2007a; Li et al., 2007b), and MTA1 protein is a direct stimulator of rhodopsin expression (Manavathi et al., 2007a). These are only a few of the known physiological functions of MTA1 protein (Toh and Nicolson, 2009), and it is expected that other MTA proteins have important roles in normal physiology and development. Thus, determining the normal physiological functions of MTA proteins will be absolutely necessary in understanding the pathological functions of MTA proteins in human cancers

Bibliography

A novel candidate metastasis-associated gene, mta1, differentially expressed in highly metastatic mammary adenocarcinoma cell lines. cDNA cloning, expression, and protein analyses.
Toh Y, Pencil SD, Nicolson GL.
J Biol Chem. 1994 Sep 16;269(37):22958-63.
PMID 8083195
 
Analysis of the complete sequence of the novel metastasis-associated candidate gene, mta1, differentially expressed in mammary adenocarcinoma and breast cancer cell lines.
Toh Y, Pencil SD, Nicolson GL.
Gene. 1995 Jun 14;159(1):97-104.
PMID 7607577
 
Involvement of heregulin-beta2 in the acquisition of the hormone-independent phenotype of breast cancer cells.
Tang CK, Perez C, Grunt T, Waibel C, Cho C, Lupu R.
Cancer Res. 1996 Jul 15;56(14):3350-8.
PMID 8764133
 
Overexpression of the MTA1 gene in gastrointestinal carcinomas: correlation with invasion and metastasis.
Toh Y, Oki E, Oda S, Tokunaga E, Ohno S, Maehara Y, Nicolson GL, Sugimachi K.
Int J Cancer. 1997 Aug 22;74(4):459-63.
PMID 9291440
 
Chromatin deacetylation by an ATP-dependent nucleosome remodelling complex.
Tong JK, Hassig CA, Schnitzler GR, Kingston RE, Schreiber SL.
Nature. 1998 Oct 29;395(6705):917-21.
PMID 9804427
 
NURD, a novel complex with both ATP-dependent chromatin-remodeling and histone deacetylase activities.
Xue Y, Wong J, Moreno GT, Young MK, Cote J, Wang W.
Mol Cell. 1998 Dec;2(6):851-61.
PMID 9885572
 
Overexpression of metastasis-associated MTA1 mRNA in invasive oesophageal carcinomas.
Toh Y, Kuwano H, Mori M, Nicolson GL, Sugimachi K.
Br J Cancer. 1999 Apr;79(11-12):1723-6.
PMID 10206283
 
Molecular association between ATR and two components of the nucleosome remodeling and deacetylating complex, HDAC2 and CHD4.
Schmidt DR, Schreiber SL.
Biochemistry. 1999 Nov 2;38(44):14711-7.
PMID 10545197
 
The Caenorhabditis elegans genes egl-27 and egr-1 are similar to MTA1, a member of a chromatin regulatory complex, and are redundantly required for embryonic patterning.
Solari F, Bateman A, Ahringer J.
Development. 1999 Jun;126(11):2483-94.
PMID 10226007
 
Mi-2 complex couples DNA methylation to chromatin remodelling and histone deacetylation.
Wade PA, Gegonne A, Jones PL, Ballestar E, Aubry F, Wolffe AP.
Nat Genet. 1999 Sep;23(1):62-6.
PMID 10471500
 
Analysis of the NuRD subunits reveals a histone deacetylase core complex and a connection with DNA methylation.
Zhang Y, Ng HH, Erdjument-Bromage H, Tempst P, Bird A, Reinberg D.
Genes Dev. 1999 Aug 1;13(15):1924-35.
PMID 10444591
 
Expression of MTA1, a metastasis-associated gene with histone deacetylase activity in pancreatic cancer.
Iguchi H, Imura G, Toh Y, Ogata Y.
Int J Oncol. 2000 Jun;16(6):1211-4.
PMID 10811997
 
Deacetylation of p53 modulates its effect on cell growth and apoptosis.
Luo J, Su F, Chen D, Shiloh A, Gu W.
Nature. 2000 Nov 16;408(6810):377-81.
PMID 11099047
 
Tumor metastasis-associated human MTA1 gene: its deduced protein sequence, localization, and association with breast cancer cell proliferation using antisense phosphorothioate oligonucleotides.
Nawa A, Nishimori K, Lin P, Maki Y, Moue K, Sawada H, Toh Y, Fumitaka K, Nicolson GL.
J Cell Biochem. 2000 Aug 2;79(2):202-12.
PMID 10967548
 
Molecular analysis of a candidate metastasis-associated gene, MTA1: possible interaction with histone deacetylase 1.
Toh Y, Kuninaka S, Endo K, Oshiro T, Ikeda Y, Nakashima H, Baba H, Kohnoe S, Okamura T, Nicolson GL, Sugimachi K.
J Exp Clin Cancer Res. 2000 Mar;19(1):105-11.
PMID 10840944
 
Role of C. elegans lin-40 MTA in vulval fate specification and morphogenesis.
Chen Z, Han M.
Development. 2001 Dec;128(23):4911-21.
PMID 11731470
 
Assignment of the human metastasis-associated gene 1 (MTA1) to human chromosome band 14q32.3 by fluorescence in situ hybridization.
Cui Q, Takiguchi S, Matsusue K, Toh Y, Yoshida MA.
Cytogenet Cell Genet. 2001;93(1-2):139-40.
PMID 11474200
 
Loss of heterozygosity events impeding breast cancer metastasis contain the MTA1 gene.
Martin MD, Fischbach K, Osborne CK, Mohsin SK, Allred DC, O'Connell P.
Cancer Res. 2001 May 1;61(9):3578-80.
PMID 11325822
 
Characterization of mouse metastasis-associated gene 2: genomic structure, nuclear localization signal, and alternative potentials as transcriptional activator and repressor.
Matsusue K, Takiguchi S, Toh Y, Kono A.
DNA Cell Biol. 2001 Oct;20(10):603-11.
PMID 11749719
 
Transcriptional repression of oestrogen receptor by metastasis-associated protein 1 corepressor.
Mazumdar A, Wang RA, Mishra SK, Adam L, Bagheri-Yarmand R, Mandal M, Vadlamudi RK, Kumar R.
Nat Cell Biol. 2001 Jan;3(1):30-7.
PMID 11146623
 
Expression of the MTA1 mRNA in thymoma patients.
Sasaki H, Yukiue H, Kobayashi Y, Nakashima Y, Kaji M, Fukai I, Kiriyama M, Yamakawa Y, Fujii Y.
Cancer Lett. 2001 Dec 28;174(2):159-63.
PMID 11689291
 
A naturally occurring MTA1 variant sequesters oestrogen receptor-alpha in the cytoplasm.
Kumar R, Wang RA, Mazumdar A, Talukder AH, Mandal M, Yang Z, Bagheri-Yarmand R, Sahin A, Hortobagyi G, Adam L, Barnes CJ, Vadlamudi RK.
Nature. 2002 Aug 8;418(6898):654-7.
PMID 12167865
 
Metastasis-associated protein (MTA)1 enhances migration, invasion, and anchorage-independent survival of immortalized human keratinocytes.
Mahoney MG, Simpson A, Jost M, Noe M, Kari C, Pepe D, Choi YW, Uitto J, Rodeck U.
Oncogene. 2002 Mar 28;21(14):2161-70.
PMID 11948399
 
Expression of the MTA1 mRNA in advanced lung cancer.
Sasaki H, Moriyama S, Nakashima Y, Kobayashi Y, Yukiue H, Kaji M, Fukai I, Kiriyama M, Yamakawa Y, Fujii Y.
Lung Cancer. 2002 Feb;35(2):149-54.
PMID 11804687
 
Connecting estrogen receptor function, transcriptional repression, and E-cadherin expression in breast cancer.
Fearon ER.
Cancer Cell. 2003 Apr;3(4):307-10. (REVIEW)
PMID 12726856
 
MTA3, a Mi-2/NuRD complex subunit, regulates an invasive growth pathway in breast cancer.
Fujita N, Jaye DL, Kajita M, Geigerman C, Moreno CS, Wade PA.
Cell. 2003 Apr 18;113(2):207-19.
PMID 12705869
 
Emerging roles of MTA family members in human cancers.
Kumar R, Wang RA, Bagheri-Yarmand R.
Semin Oncol. 2003 Oct;30(5 Suppl 16):30-7. (REVIEW)
PMID 14613024
 
MICoA, a novel metastasis-associated protein 1 (MTA1) interacting protein coactivator, regulates estrogen receptor-alpha transactivation functions.
Mishra SK, Mazumdar A, Vadlamudi RK, Li F, Wang RA, Yu W, Jordan VC, Santen RJ, Kumar R.
J Biol Chem. 2003 May 23;278(21):19209-19. Epub 2003 Mar 14.
PMID 12639951
 
Tumor metastasis-associated human MTA1 gene and its MTA1 protein product: role in epithelial cancer cell invasion, proliferation and nuclear regulation.
Nicolson GL, Nawa A, Toh Y, Taniguchi S, Nishimori K, Moustafa A.
Clin Exp Metastasis. 2003;20(1):19-24. (REVIEW)
PMID 12650603
 
Histone H4 acetylation and histone deacetylase 1 expression in esophageal squamous cell carcinoma.
Toh Y, Yamamoto M, Endo K, Ikeda Y, Baba H, Kohnoe S, Yonemasu H, Hachitanda Y, Okamura T, Sugimachi K.
Oncol Rep. 2003 Mar-Apr;10(2):333-8.
PMID 12579268
 
MTA1 interacts with MAT1, a cyclin-dependent kinase-activating kinase complex ring finger factor, and regulates estrogen receptor transactivation functions.
Talukder AH, Mishra SK, Mandal M, Balasenthil S, Mehta S, Sahin AA, Barnes CJ, Kumar R.
J Biol Chem. 2003 Mar 28;278(13):11676-85. Epub 2003 Jan 13.
PMID 12527756
 
The association of the expression of MTA1, nm23H1 with the invasion, metastasis of ovarian carcinoma.
Yi S, Guangqi H, Guoli H.
Chin Med Sci J. 2003 Jun;18(2):87-92.
PMID 12903788
 
Metastasis-associated protein 1 deregulation causes inappropriate mammary gland development and tumorigenesis.
Bagheri-Yarmand R, Talukder AH, Wang RA, Vadlamudi RK, Kumar R.
Development. 2004 Jul;131(14):3469-79.
PMID 15226262
 
Mi-2/NuRD: multiple complexes for many purposes.
Bowen NJ, Fujita N, Kajita M, Wade PA.
Biochim Biophys Acta. 2004 Mar 15;1677(1-3):52-7. (REVIEW)
PMID 15020045
 
Hormonal regulation of metastasis-associated protein 3 transcription in breast cancer cells.
Fujita N, Kajita M, Taysavang P, Wade PA.
Mol Endocrinol. 2004 Dec;18(12):2937-49. Epub 2004 Sep 9.
PMID 15358836
 
The role of metastasis-associated protein 1 in prostate cancer progression.
Hofer MD, Kuefer R, Varambally S, Li H, Ma J, Shapiro GI, Gschwend JE, Hautmann RE, Sanda MG, Giehl K, Menke A, Chinnaiyan AM, Rubin MA.
Cancer Res. 2004 Feb 1;64(3):825-9.
PMID 14871807
 
Expression of MTA1 promotes motility and invasiveness of PANC-1 pancreatic carcinoma cells.
Hofer MD, Menke A, Genze F, Gierschik P, Giehl K.
Br J Cancer. 2004 Jan 26;90(2):455-62.
PMID 14735193
 
Identification of tumour antigens by serological analysis of cDNA expression cloning.
Li G, Miles A, Line A, Rees RC.
Cancer Immunol Immunother. 2004 Mar;53(3):139-43. Epub 2004 Jan 13. (REVIEW)
PMID 14722670
 
Metastatic tumor antigen 1 short form (MTA1s) associates with casein kinase I-gamma2, an estrogen-responsive kinase.
Mishra SK, Yang Z, Mazumdar A, Talukder AH, Larose L, Kumar R.
Oncogene. 2004 May 27;23(25):4422-9.
PMID 15077195
 
Upstream determinants of estrogen receptor-alpha regulation of metastatic tumor antigen 3 pathway.
Mishra SK, Talukder AH, Gururaj AE, Yang Z, Singh RR, Mahoney MG, Franci C, Vadlamudi RK, Kumar R.
J Biol Chem. 2004 Jul 30;279(31):32709-15. Epub 2004 May 28.
PMID 15169784
 
Overexpression of metastatic tumor antigen 1 in hepatocellular carcinoma: Relationship to vascular invasion and estrogen receptor-alpha.
Moon WS, Chang K, Tarnawski AS.
Hum Pathol. 2004 Apr;35(4):424-9.
PMID 15116322
 
Metastasis-associated protein 1 interacts with NRIF3, an estrogen-inducible nuclear receptor coregulator.
Talukder AH, Gururaj A, Mishra SK, Vadlamudi RK, Kumar R.
Mol Cell Biol. 2004 Aug;24(15):6581-91.
PMID 15254226
 
Expression of the metastasis-associated MTA1 protein and its relationship to deacetylation of the histone H4 in esophageal squamous cell carcinomas.
Toh Y, Ohga T, Endo K, Adachi E, Kusumoto H, Haraguchi M, Okamura T, Nicolson GL.
Int J Cancer. 2004 Jun 20;110(3):362-7.
PMID 15095300
 
Direct interaction between metastasis-associated protein 1 and endophilin 3.
Aramaki Y, Ogawa K, Toh Y, Ito T, Akimitsu N, Hamamoto H, Sekimizu K, Matsusue K, Kono A, Iguchi H, Takiguchi S.
FEBS Lett. 2005 Jul 4;579(17):3731-6.
PMID 15978591
 
Expression analysis of a subset of coregulators and three nuclear receptors in human colorectal carcinoma.
Giannini R, Cavallini A.
Anticancer Res. 2005 Nov-Dec;25(6B):4287-92.
PMID 16309230
 
Reduced MTA1 expression by RNAi inhibits in vitro invasion and migration of esophageal squamous cell carcinoma cell line.
Qian H, Lu N, Xue L, Liang X, Zhang X, Fu M, Xie Y, Zhan Q, Liu Z, Lin C.
Clin Exp Metastasis. 2005;22(8):653-62. Epub 2006 May 16.
PMID 16703414
 
Negative regulation of estrogen receptor alpha transactivation functions by LIM domain only 4 protein.
Singh RR, Barnes CJ, Talukder AH, Fuqua SA, Kumar R.
Cancer Res. 2005 Nov 15;65(22):10594-601.
PMID 16288053
 
Metastasis-associated protein 1 (MTA1) is an essential downstream effector of the c-MYC oncoprotein.
Zhang XY, DeSalle LM, Patel JH, Capobianco AJ, Yu D, Thomas-Tikhonenko A, McMahon SB.
Proc Natl Acad Sci U S A. 2005 Sep 27;102(39):13968-73. Epub 2005 Sep 19.
PMID 16172399
 
Immunotherapeutic potential of DISC-HSV and OX40L in cancer.
Assudani DP, Ahmad M, Li G, Rees RC, Ali SA.
Cancer Immunol Immunother. 2006 Jan;55(1):104-11. Epub 2005 Oct 27. (REVIEW)
PMID 16001161
 
Expression of metastasis-associated protein 1 (MTA1) in benign endometrium and endometrial adenocarcinomas.
Balasenthil S, Broaddus RR, Kumar R.
Hum Pathol. 2006 Jun;37(6):656-61.
PMID 16733204
 
Metastasis-associated protein 2 is a repressor of estrogen receptor alpha whose overexpression leads to estrogen-independent growth of human breast cancer cells.
Cui Y, Niu A, Pestell R, Kumar R, Curran EM, Liu Y, Fuqua SA.
Mol Endocrinol. 2006 Sep;20(9):2020-35. Epub 2006 Apr 27.
PMID 16645043
 
Breast cancer-amplified sequence 3, a target of metastasis-associated protein 1, contributes to tamoxifen resistance in premenopausal patients with breast cancer.
Gururaj AE, Holm C, Landberg G, Kumar R.
Cell Cycle. 2006a Jul;5(13):1407-10. Epub 2006 Jul 1.
PMID 16855396
 
MTA1, a transcriptional activator of breast cancer amplified sequence 3.
Gururaj AE, Singh RR, Rayala SK, Holm C, den Hollander P, Zhang H, Balasenthil S, Talukder AH, Landberg G, Kumar R.
Proc Natl Acad Sci U S A. 2006b Apr 25;103(17):6670-5. Epub 2006 Apr 14.
PMID 16617102
 
Comprehensive analysis of the expression of the metastasis-associated gene 1 in human neoplastic tissue.
Hofer MD, Tapia C, Browne TJ, Mirlacher M, Sauter G, Rubin MA.
Arch Pathol Lab Med. 2006 Jul;130(7):989-96.
PMID 16831056
 
MTA1 overexpression correlates significantly with tumor grade and angiogenesis in human breast cancers.
Jang KS, Paik SS, Chung H, Oh YH, Kong G.
Cancer Sci. 2006 May;97(5):374-9.
PMID 16630134
 
The role of genetic markers--NAP1L1, MAGE-D2, and MTA1--in defining small-intestinal carcinoid neoplasia.
Kidd M, Modlin IM, Mane SM, Camp RL, Eick G, Latich I.
Ann Surg Oncol. 2006a Feb;13(2):253-62. Epub 2006 Jan 20.
PMID 16424981
 
Utility of molecular genetic signatures in the delineation of gastric neoplasia.
Kidd M, Modlin IM, Mane SM, Camp RL, Eick GN, Latich I, Zikusoka MN.
Cancer. 2006b Apr 1;106(7):1480-8.
PMID 16502410
 
Breast tumors that overexpress nuclear metastasis-associated 1 (MTA1) protein have high recurrence risks but enhanced responses to systemic therapies.
Martin MD, Hilsenbeck SG, Mohsin SK, Hopp TA, Clark GM, Osborne CK, Allred DC, O'Connell P.
Breast Cancer Res Treat. 2006 Jan;95(1):7-12. Epub 2005 Oct 22.
PMID 16244788
 
Genetic differentiation of appendiceal tumor malignancy: a guide for the perplexed.
Modlin IM, Kidd M, Latich I, Zikusoka MN, Eick GN, Mane SM, Camp RL.
Ann Surg. 2006a Jul;244(1):52-60.
PMID 16794389
 
The functional characterization of normal and neoplastic human enterochromaffin cells.
Modlin IM, Kidd M, Pfragner R, Eick GN, Champaneria MC.
J Clin Endocrinol Metab. 2006b Jun;91(6):2340-8. Epub 2006 Mar 14.
PMID 16537680
 
Metastasis-associated protein 1 enhances angiogenesis by stabilization of HIF-1alpha.
Moon HE, Cheon H, Chun KH, Lee SK, Kim YS, Jung BK, Park JA, Kim SH, Jeong JW, Lee MS.
Oncol Rep. 2006 Oct;16(4):929-35.
PMID 16969516
 
Maintenance of head and neck tumor gene expression profiles upon lymph node metastasis.
Roepman P, de Jager A, Groot Koerkamp MJ, Kummer JA, Slootweg PJ, Holstege FC.
Cancer Res. 2006 Dec 1;66(23):11110-4.
PMID 17145852
 
Solution structure and antiestrogenic activity of the unique C-terminal, NR-box motif-containing region of MTA1s.
Singh RR, Kaluarachchi K, Chen M, Rayala SK, Balasenthil S, Ma J, Kumar R.
J Biol Chem. 2006 Sep 1;281(35):25612-21. Epub 2006 Jun 27.
PMID 16807247
 
Metastasis-associated protein 1 enhances stability of hypoxia-inducible factor-1alpha protein by recruiting histone deacetylase 1.
Yoo YG, Kong G, Lee MO.
EMBO J. 2006 Mar 22;25(6):1231-41. Epub 2006 Mar 2.
PMID 16511565
 
Metastatic tumor antigen 3 is a direct corepressor of the Wnt4 pathway.
Zhang H, Singh RR, Talukder AH, Kumar R.
Genes Dev. 2006 Nov 1;20(21):2943-8. Epub 2006 Oct 18.
PMID 17050676
 
Metastasis-associated protein 1 transgenic mice: a new model of spontaneous B-cell lymphomas.
Bagheri-Yarmand R, Balasenthil S, Gururaj AE, Talukder AH, Wang YH, Lee JH, Kim YS, Zhang X, Jones DM, Medeiros LJ, Stephens LC, Liu YJ, Lee N, Kim I, Kumar R.
Cancer Res. 2007 Aug 1;67(15):7062-7.
PMID 17671172
 
Identification of Pax5 as a target of MTA1 in B-cell lymphomas.
Balasenthil S, Gururaj AE, Talukder AH, Bagheri-Yarmand R, Arrington T, Haas BJ, Braisted JC, Kim I, Lee NH, Kumar R.
Cancer Res. 2007 Aug 1;67(15):7132-8.
PMID 17671180
 
Small bowel carcinoid (enterochromaffin cell) neoplasia exhibits transforming growth factor-beta1-mediated regulatory abnormalities including up-regulation of C-Myc and MTA1.
Kidd M, Modlin IM, Pfragner R, Eick GN, Champaneria MC, Chan AK, Camp RL, Mane SM.
Cancer. 2007 Jun 15;109(12):2420-31.
PMID 17469181
 
Correlation of appearance of metastasis-associated protein1 (Mta1) with spermatogenesis in developing mouse testis.
Li W, Zhang J, Liu X, Xu R, Zhang Y.
Cell Tissue Res. 2007a Aug;329(2):351-62. Epub 2007 Apr 2.
PMID 17401724
 
Immunolocalization assessment of metastasis-associated protein 1 in human and mouse mature testes and its association with spermatogenesis.
Li W, Liu XP, Xu RJ, Zhang YQ.
Asian J Androl. 2007b May;9(3):345-52.
PMID 17486275
 
Metastasis tumor antigens, an emerging family of multifaceted master coregulators.
Manavathi B, Kumar R.
J Biol Chem. 2007 Jan 19;282(3):1529-33. Epub 2006 Dec 1.
PMID 17142453
 
Repression of Six3 by a corepressor regulates rhodopsin expression.
Manavathi B, Peng S, Rayala SK, Talukder AH, Wang MH, Wang RA, Balasenthil S, Agarwal N, Frishman LJ, Kumar R.
Proc Natl Acad Sci U S A. 2007a Aug 7;104(32):13128-33. Epub 2007 Jul 31.
PMID 17666527
 
MTA family of coregulators in nuclear receptor biology and pathology.
Manavathi B, Singh K, Kumar R.
Nucl Recept Signal. 2007b Nov 30;5:e010. (REVIEW)
PMID 18174918
 
Metastasis-associated protein 1 inhibits p53-induced apoptosis.
Moon HE, Cheon H, Lee MS.
Oncol Rep. 2007 Nov;18(5):1311-4.
PMID 17914590
 
RNA interference of metastasis-associated gene 1 inhibits metastasis of B16F10 melanoma cells in a C57BL/6 mouse model.
Qian H, Yu J, Li Y, Wang H, Song C, Zhang X, Liang X, Fu M, Lin C.
Biol Cell. 2007 Oct;99(10):573-81.
PMID 17868030
 
MTA family of transcriptional metaregulators in mammary gland morphogenesis and breast cancer.
Singh RR, Kumar R.
J Mammary Gland Biol Neoplasia. 2007 Sep;12(2-3):115-25. (REVIEW)
PMID 17549610
 
Heat shock factor 1 represses estrogen-dependent transcription through association with MTA1.
Khaleque MA, Bharti A, Gong J, Gray PJ, Sachdev V, Ciocca DR, Stati A, Fanelli M, Calderwood SK.
Oncogene. 2008 Mar 20;27(13):1886-93. Epub 2007 Oct 8.
PMID 17922035
 
Expression of hypoxia-inducible factor-1alpha, histone deacetylase 1, and metastasis-associated protein 1 in pancreatic carcinoma: correlation with poor prognosis with possible regulation.
Miyake K, Yoshizumi T, Imura S, Sugimoto K, Batmunkh E, Kanemura H, Morine Y, Shimada M.
Pancreas. 2008 Apr;36(3):e1-9.
PMID 18362831
 
MTA1-mediated transcriptional repression of BRCA1 tumor suppressor gene.
Molli PR, Singh RR, Lee SW, Kumar R.
Oncogene. 2008 Mar 27;27(14):1971-80. Epub 2007 Oct 8.
PMID 17922032
 
Metastatic tumor antigen 1 is closely associated with frequent postoperative recurrence and poor survival in patients with hepatocellular carcinoma.
Ryu SH, Chung YH, Lee H, Kim JA, Shin HD, Min HJ, Seo DD, Jang MK, Yu E, Kim KW.
Hepatology. 2008 Mar;47(3):929-36.
PMID 18306220
 
Hepatitis B virus X protein induces the expression of MTA1 and HDAC1, which enhances hypoxia signaling in hepatocellular carcinoma cells.
Yoo YG, Na TY, Seo HW, Seong JK, Park CK, Shin YK, Lee MO.
Oncogene. 2008 May 29;27(24):3405-13. Epub 2008 Feb 11.
PMID 18264140
 
MTA1 coregulator regulates p53 stability and function.
Li DQ, Divijendra Natha Reddy S, Pakala SB, Wu X, Zhang Y, Rayala SK, Kumar R.
J Biol Chem. 2009a Dec 11;284(50):34545-52. Epub 2009 Oct 16.
PMID 19837670
 
E3 ubiquitin ligase COP1 regulates the stability and functions of MTA1.
Li DQ, Ohshiro K, Reddy SD, Pakala SB, Lee MH, Zhang Y, Rayala SK, Kumar R.
Proc Natl Acad Sci U S A. 2009b Oct 13;106(41):17493-8. Epub 2009 Sep 24.
PMID 19805145
 
MicroRNA-661, a c/EBPalpha target, inhibits metastatic tumor antigen 1 and regulates its functions.
Reddy SD, Pakala SB, Ohshiro K, Rayala SK, Kumar R.
Cancer Res. 2009 Jul 15;69(14):5639-42. Epub 2009 Jul 7.
PMID 19584269
 
The role of the MTA family and their encoded proteins in human cancers: molecular functions and clinical implications.
Toh Y, Nicolson GL.
Clin Exp Metastasis. 2009;26(3):215-27. Epub 2008 Dec 31. (REVIEW)
PMID 19116762
 
Written2010-06Yasushi Toh, Garth L Nicolson
of Gastroenterological Surgery, National Kyushu Cancer Center, Fukuoka, 811-1395, Japan (YT); Department of Molecular Pathology, The Institute for Molecular Medicine, Huntington Beach, CA 92647, USA (GLN)

Citation

This paper should be referenced as such :
Toh, Y ; Nicolson, GL
MTA1 of the MTA (metastasis-associated) gene family, its encoded proteins: molecular, regulatory functions, role in human cancer progression
Atlas Genet Cytogenet Oncol Haematol. 2011;15(3):303-315.
Free journal version : [ pdf ]   [ DOI ]
On line version : http://AtlasGeneticsOncology.org/Deep/MTAinCancerID20088.htm

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