- freely available
Int. J. Mol. Sci. 2013, 14(12), 23231-23243; doi:10.3390/ijms141223231
Abstract: The HOP (homeobox only protein) homeobox (HOPX) is most closely related to the homeobox protein that contains a homeobox-like domain but lacks certain conserved residues required for DNA binding. Here, we review the current understanding of HOPX in the progression of colorectal cancer (CRC). HOPX was initially reported as a differentiation marker and is expressed in various normal tissues. In the colon, HOPX is expressed uniquely in the quiescent stem cell, +4, and in differentiated mucosal cells of the colon. HOPX expression is markedly suppressed in a subset of cancers, mainly in an epigenetic manner. CRC may include separate entities which are differentially characterized by HOPX expression from a prognostic point of view. HOPX itself can regulate epigenetics, and defective expression of HOPX can result in loss of tumor suppressive function and differentiation phenotype. These findings indicate that HOPX may be both a central regulator of epigenetic dynamics and a critical determinant for differentiation in human cells. HOPX downstream targets were identified in CRC cell lines and hold promise as candidates for therapeutic targets of CRC, such as EphA2 or AP-1. Further analysis will elucidate and confirm the precise role of such proteins in CRC progression.
HOP (homeobox only protein) homeobox (HOPX) was identified in mouse and humans by searching an EST database using the PAX3 homeobox as a probe . The human and mouse HOPX proteins contain 73 amino acids, including a 60 amino acid motif homologous to HOX proteins, and share 92% identity. The mouse and human HOPX proteins are most closely related to the homeobox protein HOX6 and goosecoid, sharing approximately 40% identity within the homeobox-like domain (Figure 1a). HOPX lacks certain conserved residues required for DNA binding. In mouse, HOPX gene expression is initiated early in cardiogenesis and continues in cardiomyocytes throughout embryonic and postnatal development. Northern blot analysis of adult and embryonic mouse tissues detected a 1.2-kb transcript in embryonic and adult heart and in adult brain, lung, liver, intestine, and spleen . Shin et al. independently cloned mouse HOPX and identified the human homolog . They determined that HOPX forms three alpha helices which fold into a helix-turn-helix motif characteristic of the homeobox (Figure 1b).
HOPX is highly expressed in the developing heart, where its expression is dependent on the cardiac-restricted homeobox protein, Nkx2.5. Genetic and biochemical data indicate that mouse HOPX functions directly downstream of Nkx2.5, and that HOPX physically interacts with serum responsive factor (SRF) and inhibits SRF-dependent transcription by inhibiting SRF binding to DNA . Shin et al. confirmed that mouse HOPX does not bind DNA and acts as an antagonist of SRF, which regulates the opposing processes of proliferation and myogenesis . Kook et al. also showed that HOPX can inhibit SRF-dependent transcriptional activation by recruiting histone deacetylase (HDAC) activity and can form a complex that includes HDAC2 [3,4]. Transgenic mice overexpressing HOPX develop severe cardiac hypertrophy, cardiac fibrosis, and die prematurely. A mutant form of HOPX, which does not recruit HDAC activity, did not induce hypertrophy. Kook et al. therefore concluded that chromatin remodeling and repression of active transcriptional processes can result in hypertrophy and heart failure; intriguingly, this process can be blocked with chemical HDAC inhibitors.
Kee et al. used yeast 2-hybrid analysis to identify enhancer of polycomb 1 (EPC1), which interacts with HOPX. Expression of EPC1 was upregulated during differentiation of a rat myoblast cell line into skeletal myocytes . Differentiation was induced by EPC1 overexpression, and was severely impaired in EPC1-knockdown cells. Cotransfection of HOPX potentiated EPC1-induced transactivation of myogenin and myotube formation. Kee et al. concluded that EPC1 plays a role in initiation of skeletal muscle differentiation and that its interaction with HOPX is required for full activity. Hence, the function of HOPX is to regulate epigenetics (Figure 2).
HOPX has been reported to play a critical role in the differentiation of various cells such as trophoblasts [6,7], keratinocytes [8,9], T cells [10,11] and lung alveolar cells . Most intriguingly, HOPX is strongly expressed in quiescent colon stem cells  and hair follicle cells .
2. Genomic Structure of HOPX Gene
The International Radiation Hybrid Mapping Consortium mapped the HOPX gene to chromosome 4 (Figure 3a). Previous studies using comparative genomic hybridization have reported copy number loss at this region in hepatocellular carcinoma [15,16]. Loss of heterozygosity (LOH) at 4q12–q13 was also identified in breast  and hepatocellular carcinomas . LOH analysis was performed using three microsatellite markers, D4S189, D4S231 and D4S392, around the region of chromosome 4q12 in 29 paired primary lung tumor samples, where HOP locates. LOH was found in 4 out of 23 cases (17.4%) . These findings suggest the existence of a tumor suppressor gene at 4q11–q13, with HOPX being one of the candidate genes. Although HOPX has three spliced variants, the coded proteins are identical (HOP core). The location of CpGs in the HOPX genomic sequence is shown in Figure 3b. Of the three spliced transcript variants, only HOPX-β promoter harbors CpG islands encompassing the first exon and intron, whereas the same promoter for HOPX-α and HOPX-γ does not harbor any CpG islands near the transcription start site.
3. Colorectal Cancer (CRC) and HOPX Gene Expression
HOPX is strongly expressed in normal colorectal mucosa tissues, and this Immunohistochemical staining is absorbed by HOPX peptide pretreatment, as previously reported  (Figure 1c). On the other hand, HOPX expression is dramatically downregulated in subsets of primary CRC (Figure 1d). Recent examination of cancer genetics data revealed that down-regulation of important tumor suppressor genes is often caused by DNA hypermethylation of promoter CpG islands in a cancer-specific manner. HOPX is one of these tabulated genes [20,22–24]. Specifically, the expression of HOPX is suppressed in various primary cancer tissues [12,20,21,23,25–29] (Table 1). Among these cancers, DNA methylation is prevalent in esophagus , stomach , and pancreas  cancers, as well as colorectal cancer (CRC) .
CRC is a well-studied cancer in which both gene expression and DNA methylation status have been examined. In CRC, HOPX methylation status reflects HOPX expression levels well . Specifically, primary CRC tissues or colorectal mucosa tissues with HOPX hypermethylation show a low level of HOPX expression, and vice versa. More intriguingly, the demethylating agent 5-aza-2′-deoxycytidine, and/or the HDAC inhibitor trichostatin A, robustly reactivated HOPX expression. Reactivation was especially pronounced for HOPX-β, which harbors CpG islands in the CRC cell lines, DLD1 and HCT116. These findings suggest that HOPX expression is regulated mainly by epigenetic control in CRC.
Quantitative TaqMan MSP (methylation specific PCR) showed significantly higher methylation levels in primary CRC tissues than in the corresponding normal mucosal tissues . This analysis further elucidated that the HOPX methylation value significantly increases during progression from non-metastatic disease (pN0) to metastatic disease (pN1) in CRC. Even in patients with primary CRC and positive lymph nodes (Stage III), patients with higher HOPX methylation showed poorer prognosis than those with lower HOPX methylation. These findings suggest that HOPX hypermethylation represents an aggressive phenotype of CRC.
On the other hand, poorly differentiated CRC is relatively rare among CRC, and is characterized by dismal prognosis as compared with differentiated CRC. It is intriguing that poorly differentiated CRC harbors more highly hypermethylated HOPX than differentiated CRC [26,30].
4. Functional Role of HOPX in CRC
Cancer-specific hypermethylation of CpG islands of the promoter regions suggests that such genes have tumor suppressor function [22,31,32]. HOPX has been demonstrated to have tumor suppressor function in various cancers, including CRC (Table 2). Asanoma et al. (2003) transfected HOPX into choriocarcinoma cell lines and observed remarkable alterations in cell morphology and suppression of in vivo tumorigenesis . In vitro or in vivo tumorigenesis has been repeatedly proven to be suppressed by HOPX gene transfection in esophageal cancer , endometrial cancer , gastric cancer , and pancreatic cancer . In the CRC cell lines, DLD1 and HCT116, HOPX transfection strongly suppressed tumorigenesis in nude mice and in a soft agar assay . In DLD1 transfected with HOPX, stromal angiogenesis on day 15 was remarkably suppressed. Moreover, TUNEL assay was performed in tumors derived from HOPX or mock transfected DLD1, and apoptotic cells were significantly more recognized in HOPX transfected cells than in mock cells. Cell cycle analysis showed that HOPX transfection increased the subG1 population and the level of caspase-3 is higher in HOPX-transfected cells than in mock cells. These findings strongly indicate that HOPX is a tumor suppressor gene in CRC.
HOPX may be involved in cell invasiveness in CRC and other cancers [12,20,21]. Matrigel invasion assays of CRC cell lines showed that HOPX transfection results in a remarkable reduction of invaded cells . F-actin labeling with Phalloidin revealed that the mock cells exhibited active filopodia, whereas HOPX-expressing cells exhibited fewer filopodia fibers and showed F-actin aggregated in the cytoplasm. Recent reports studying other cancers demonstrated the mechanism of augmented cancer invasion in HOPX knockdown cells; for example, HOPX knockdown is involved in marked phosphorylation of FAK (focal adhesion kinase) and integrin α5 in human lung cancer . In a recent report on sarcoma cells, down-regulation of the HOPX gene unexpectedly decreased metastatic activity and identified genes associated with metastasis, such as integrin α 4 . Given the prognostic relevance of HOPX in primary CRC, and findings obtained from basic research on the role of HPOX in cancer not including sarcoma, HOPX is likely implicated in the suppression of metastasis of CRC.
5. Downstream Gene of HOPX in CRC
Since HOPX is involved in epigenetic regulation of differentiation-associated genes (Figure 2), the downstream targets of HOPX may include critical onco-proteins. However, there have been few reports describing downstream genes of HOPX in human cancers [12,26]. In CRC, expression microarray revealed that HOPX down-regulated oncoproteins. Cyr61, EMP1, EphA2, c-Fos, c-Jun, EGR1, and GLUT3 were identified as candidate genes  (Figure 4). Of these, c-Fos has been repeatedly described as a HOPX downstream gene in non-colonic cells such as endometrial cancer  and regulatory T cells (Treg) .
c-Fos is a component of AP-1 transcriptional factor and forms a heterodimer with c-Jun. HOPX-sufficient iT(reg) cells downregulated expression of the transcription factor AP-1 complex and suppressed other T cells . In human cancer cells such as HEC and MCF7, forced expression of HOPX resulted in a partial block in cell proliferation, in vivo tumorigenicity, and c-fos gene expression in response to 17 beta estradiol (E2) stimulation . In these cancer cells, analysis of the serum response element (SRE) of c-fos gene promoter showed that the effect of HOPX expression is associated with inhibition of E(2)-induced c-fos activation through the serum response factor (SRF) motif. These findings suggest that AP-1 is a critical downstream protein of HOPX through SRF. Transcription factor-binding sites of AP-1 are frequently recognized in the promoter region of cancer metastasis-associated genes such as matrix metalloproteinases [34,35] and tumor growth factors/receptors  (Figure 5). Consequently, such transcription factors could be decisive therapeutic targets in CRC. EGR-1 is another transcription factor downstream of HOPX that controls cancer progression through induction of IGF-II, , PDGF , and TGF-beta .
Tyrosine kinases such as EphA2 or EMP1 could be very interesting targets in cancer therapy because these cell surface molecules are more appropriate therapeutic targets than transcription factors. EphA2 is over-expressed in patients with HOPX hypermethylation . Recent studies demonstrated that EphA2 is over-expressed in human cancers, and that EphA2 increases tumor invasion and survival, including of patients with CRC [40,41]. Thus, an EphA2 receptor antagonist, such as a specific tyrosine kinase inhibitor (in the form of an antibody, small molecule, peptide, or siRNA), or an antibody-drug conjugate that targets the EphA2 receptor, could be the basis for a novel targeted antineoplastic therapy [42–45]. EMP1 is an adhesion molecule that has been correlated with a lack of complete or partial response to gefitinib in lung cancer patient samples, as well as clinical progression to secondary gefitinib resistance. These findings suggest probable cross-talk between EMP1 and the EGFR signaling pathway . EGFR could be an optimal target of CRC. EGFR antibodies (cetuximab and panitumumab) are active against CRC with no K-ras mutation [47,48], suggesting that EMP-1 holds promise as a predictive biomarker in antibody therapy.
In CRC, abundant expression of Cyr61 is found in patients with HOPX hypermethylation (Figure 4d) . Cyr61/CCN1 is a matricellular protein and a member of the CCN family of growth factors. It is a critical downstream contributor to sonic hedgehog (SHh) that influences the pro-angiogenic tumor microenvironment . CCN1-induced activation of SHh signaling may be necessary for CCN1-dependent in vitro cancer cell migration and tumorigenicity of cancer stem cells in a xenograft in nude mice .
Importantly, HOPX is likely to suppress independent oncogenic pathways, so multi-pathway inhibition may be required to control CRC with HOPX hypermethylation and silenced expression (Figure 5).
6. Quiescent Stem Cell (+4) and HOPX in Colon Goblet Cells
In colonic mucosa, cells in the +4 niche are slow-cycling and label-retaining, whereas a different stem cell niche located at the crypt base is occupied by crypt base columnar (CBC) cells (Figure 6). It was recently reported that HOPX is a specific marker of quiescent stem cells (+4), while Lgr-5 is a specific marker of active stem cells in the colon mucosa [13,51]. CBCs are distinct from +4 cells, although both give rise to all intestinal epithelial lineages. Takeda et al. demonstrated that HOPX-expressing cells give rise to CBCs and all mature intestinal epithelial lineages. Conversely, CBCs can give rise to +4 HOPX-positive cells . These findings demonstrate a bidirectional lineage relationship between active and quiescent stem cells in their niches, although it is unknown whether HOPX is epigenetically regulated or not in the colon stem cells.
In CRC, overexpression of LGR5 was significantly associated with expression of c-MYC, p21CIP1/WAF1/CDKN1A, and GLS, and inversely associated with miR-23a/b . Immunohistochemical analysis indicated that Lgr5 may be embedded in benign adenomas, localized at the tumor-host interface, and detectable over a broad area in established tumors. A high level of LGR5 expression was associated with poor prognosis for CRC cancer patients who were curatively resected. Hence, the aggressiveness of CRC may be determined by the composite proportion of stem cells from which the cancer is generated.
In this article, we reviewed the current understanding of the relationship between HOPX and CRC. HOPX was initially reported as a differentiation marker of various tissues, and is expressed in normal organ tissues. In colon, HOPX is a quiescent colon stem cell marker and is expressed in differentiated colonic mucosa. The expression of HOPX is marked suppressed in a subset of cancers, mainly in an epigenetic manner. CRC may include separate entities which are differentially characterized by HOPX expression from a prognostic point of view. HOPX downstream targets were identified in CRC cell lines and primary CRC and could hold promise as candidates for therapeutic targets of CRC such as EphA2 or AP-1. Further analysis would elucidate and confirm the precise role of such protein molecules in CRC progression and their possible therapeutic value.
Conflicts of Interest
The authors declare no conflict of interest.
- Chen, F.; Kook, H.; Milewski, R.; Gitler, A.D.; Lu, M.M.; Li, J.; Nazarian, R.; Schnepp, R.; Jen, K.; Biben, C.; et al. Hop is an unusual homeobox gene that modulates cardiac development. Cell 2002, 110, 713–723. [Google Scholar]
- Shin, C.H.; Liu, Z.P.; Passier, R.; Zhang, C.L.; Wang, D.Z.; Harris, T.M.; Yamagishi, H.; Richardson, J.A.; Childs, G.; Olson, E.N. Modulation of cardiac growth and development by HOP, an unusual homeodomain protein. Cell 2002, 110, 725–735. [Google Scholar]
- Kook, H.; Lepore, J.J.; Gitler, A.D.; Lu, M.M.; Wing-Man Yung, W.; Mackay, J.; Zhou, R.; Ferrari, V.; Gruber, P.; Epstein, J.A. Cardiac hypertrophy and histone deacetylase-dependent transcriptional repression mediated by the atypical homeodomain protein Hop. J. Clin. Investig 2003, 112, 863–871. [Google Scholar]
- Trivedi, C.M.; Zhu, W.; Wang, Q.; Jia, C.; Kee, H.J.; Li, L.; Hannenhalli, S.; Epstein, J.A. Hopx and Hdac2 interact to modulate Gata4 acetylation and embryonic cardiac myocyte proliferation. Dev. Cell 2010, 19, 450–459. [Google Scholar]
- Kee, H.J.; Kim, J.R.; Nam, K.I.; Park, H.Y.; Shin, S.; Kim, J.C.; Shimono, Y.; Takahashi, M.; Jeong, M.H.; Kim, N.; et al. Enhancer of polycomb1, a novel homeodomain only protein-binding partner, induces skeletal muscle differentiation. J. Biol. Chem 2007, 282, 7700–7709. [Google Scholar]
- Asanoma, K.; Kato, H.; Inoue, T.; Matsuda, T.; Wake, N. Analysis of a candidate gene associated with growth suppression of choriocarcinoma and differentiation of trophoblasts. J. Reprod. Med 2004, 49, 617–626. [Google Scholar]
- Asanoma, K.; Kato, H.; Yamaguchi, S.; Shin, C.H.; Liu, Z.P.; Kato, K.; Inoue, T.; Miyanari, Y.; Yoshikawa, K.; Sonoda, K.; et al. HOP/NECC1, a novel regulator of mouse trophoblast differentiation. J. Biol. Chem 2007, 282, 24065–24074. [Google Scholar]
- Yang, J.M.; Sim, S.M.; Kim, H.Y.; Park, G.T. Expression of the homeobox gene, HOPX, is modulated by cell differentiation in human keratinocytes and is involved in the expression of differentiation markers. Eur. J. Cell Biol 2010, 89, 537–546. [Google Scholar]
- Obarzanek-Fojt, M.; Favre, B.; Kypriotou, M.; Ryser, S.; Huber, M.; Hohl, D. Homeodomain-only protein HOP is a novel modulator of late differentiation in keratinocytes. Eur. J. Cell Biol 2011, 90, 279–290. [Google Scholar]
- Hawiger, D.; Wan, Y.Y.; Eynon, E.E.; Flavell, R.A. The transcription cofactor Hopx is required for regulatory T cell function in dendritic cell-mediated peripheral T cell unresponsiveness. Nat. Immunol 2010, 11, 962–968. [Google Scholar]
- Albrecht, I.; Niesner, U.; Janke, M.; Menning, A.; Loddenkemper, C.; Kühl, A.A.; Lepenies, I.; Lexberg, M.H.; Westendorf, K.; Hradilkova, K.; et al. Persistence of effector memory Th1 cells is regulated by Hopx. Eur. J. Immunol 2010, 40, 2993–3006. [Google Scholar]
- Cheung, W.K.; Zhao, M.; Liu, Z.; Stevens, L.E.; Cao, P.D.; Fang, J.E.; Westbrook, T.F.; Nguyen, D.X. Control of alveolar differentiation by the lineage transcription factors GATA6 and HOPX inhibits lung adenocarcinoma metastasis. Cancer Cell 2013, 23, 725–738. [Google Scholar]
- Takeda, N.; Jain, R.; LeBoeuf, M.R.; Wang, Q.; Lu, M.M.; Epstein, J.A. Interconversion between intestinal stem cell populations in distinct niches. Science 2011, 334, 1420–1424. [Google Scholar]
- Takeda, N.; Jain, R.; Leboeuf, M.R.; Padmanabhan, A.; Wang, Q.; Li, L.; Lu, M.M.; Millar, S.E.; Epstein, J.A. Hopx expression defines a subset of multipotent hair follicle stem cells and a progenitor population primed to give rise to K6+ niche cells. Development 2013, 140, 1655–1664. [Google Scholar]
- Sakakura, C.; Hagiwara, A.; Taniguchi, H.; Yamaguchi, T.; Yamagishi, H.; Takahashi, T.; Koyama, K.; Nakamura, Y.; Abe, T.; Inazawa, J. Chromosomal aberrations in human hepatocellular carcinomas associated with hepatitis C virus infection detected by comparative genomic hybridization. Br. J. Cancer 1999, 80, 2034–2039. [Google Scholar]
- Wong, N.; Lai, P.; Lee, S.W.; Fan, S.; Pang, E.; Liew, C.T.; Sheng, Z.; Lau, J.W.; Johnson, P.J. Assessment of genetic changes in hepatocellular carcinoma by comparative genomic hybridization analysis: Relationship to disease stage, tumor size, and cirrhosis. Am. J. Pathol 1999, 154, 37–43. [Google Scholar]
- Burger, A.M.; Zhang, X.; Li, H.; Ostrowski, J.L.; Beatty, B.; Venanzoni, M.; Papas, T.; Seth, A. Down-regulation of T1A12/mac25, a novel insulin-like growth factor binding protein related gene, is associated with disease progression in breast carcinomas. Oncogene 1998, 16, 2459–2467. [Google Scholar]
- Leon, M.; Kew, M.C. Loss of heterozygosity in chromosome 4q12–q13 in hepatocellular carcinoma in southern African blacks. Anticancer Res 1996, 16, 349–351. [Google Scholar]
- Chen, Y.; Pacyna-Gengelbach, M.; Deutschmann, N.; Niesporek, S.; Petersen, I. Homeobox gene HOP has a potential tumor suppressive activity in human lung cancer. Int. J. Cancer 2007, 121, 1021–1027. [Google Scholar]
- Ooki, A.; Yamashita, K.; Kikuchi, S.; Sakuramoto, S.; Katada, N.; Kokubo, K.; Kobayashi, H.; Kim, M.S.; Sidransky, D.; Watanabe, M. Potential utility of HOP homeobox gene promoter methylation as a marker of tumor aggressiveness in gastric cancer. Oncogene 2010, 29, 3263–3275. [Google Scholar]
- Waraya, M.; Yamashita, K.; Katoh, H.; Ooki, A.; Kawamata, H.; Nishimiya, H.; Nakamura, K.; Ema, A.; Watanabe, M. Cancer specific promoter CpG Islands hypermethylation of HOP homeobox (HOPX) gene and its potential tumor suppressive role in pancreatic carcinogenesis. BMC Cancer 2012, 12. [Google Scholar] [CrossRef]
- Yamashita, K.; Upadhyay, S.; Osada, M.; Hoque, M.O.; Xiao, Y.; Mori, M.; Sato, F.; Meltzer, S.J.; Sidransky, D. Pharmacologic unmasking of epigenetically silenced tumor suppressor genes in esophageal squamous cell carcinoma. Cancer Cell 2002, 2, 485–495. [Google Scholar]
- Yamashita, K.; Kim, M.S.; Park, H.L.; Tokumaru, Y.; Osada, M.; Inoue, H.; Mori, M.; Sidransky, D. HOP/OB1/NECC1 promoter DNA is frequently hypermethylated and involved in tumorigenic ability in esophageal squamous cell carcinoma. Mol. Cancer Res 2008, 6, 31–41. [Google Scholar]
- Yamashita, K.; Sakuramoto, S.; Watanabe, M. Genomic and epigenetic profiles of gastric cancer: Potential diagnostic and therapeutic applications. Surg. Today 2011, 41, 24–38. [Google Scholar]
- Lemaire, F.; Millon, R.; Muller, D.; Rabouel, Y.; Bracco, L.; Abecassis, J.; Wasylyk, B. Loss of HOP tumour suppressor expression in head and neck squamous cell carcinoma. Br. J. Cancer 2004, 91, 258–261. [Google Scholar]
- Katoh, H.; Yamashita, K.; Waraya, M.; Margalit, O.; Ooki, A.; Tamaki, H.; Sakagami, H.; Kokubo, K.; Sidransky, D.; Watanabe, M. Epigenetic silencing of HOPX promotes cancer progression in colorectal cancer. Neoplasia 2012, 14, 559–571. [Google Scholar]
- Chen, Y.; Petersen, S.; Pacyna-Gengelbach, M.; Pietas, A.; Petersen, I. Identification of a novel homeobox-containing gene, LAGY, which is downregulated in lung cancer. Oncology 2003, 64, 450–458. [Google Scholar]
- Asanoma, K.; Matsuda, T.; Kondo, H.; Kato, K.; Kishino, T.; Niikawa, N.; Wake, N.; Kato, H. NECC1, a candidate choriocarcinoma suppressor gene that encodes a homeodomain consensus motif. Genomics 2003, 81, 15–25. [Google Scholar]
- Yamaguchi, S.; Asanoma, K.; Takao, T.; Kato, K.; Wake, N. Homeobox gene HOPX is epigenetically silenced in human uterine endometrial cancer and suppresses estrogen-stimulated proliferation of cancer cells by inhibiting serum response factor. Int. J. Cancer 2009, 124, 2577–2588. [Google Scholar]
- Harada, Y.; Kijima, K.; Shinmura, K.; Sakata, M.; Sakuraba, K.; Yokomizo, K.; Kitamura, Y.; Shirahata, A.; Goto, T.; Mizukami, H.; et al. Methylation of the homeobox gene, HOPX, is frequently detected in poorly differentiated colorectal cancer. Anticancer Res 2011, 31, 2889–2892. [Google Scholar]
- Kim, M.S.; Yamashita, K.; Baek, J.H.; Park, H.L.; Carvalho, A.L.; Osada, M.; Hoque, M.O.; Upadhyay, S.; Mori, M.; Moon, C.; et al. N-methyl-d-aspartate receptor type 2B is epigenetically inactivated and exhibits tumor-suppressive activity in human esophageal cancer. Cancer Res 2006, 66, 3409–3418. [Google Scholar]
- Kim, M.S.; Lee, J.; Sidransky, D. DNA methylation markers in colorectal cancer. Cancer Metastasis Rev 2010, 29, 181–206. [Google Scholar]
- Kovarova, D.; Plachy, J.; Kosla, J.; Trejbalova, K.; Cermak, V.; Hejnar, J. Downregulation of the HOPX gene decreases metastatic activity in a chicken sarcoma cell line model and identifies genes associated with metastasis. Mol. Cancer Res 2013, 11, 1235–1247. [Google Scholar]
- Crowe, D.L.; Brown, T.N. Transcriptional inhibition of matrix metalloproteinase 9 (MMP-9) activity by a c-fos/estrogen receptor fusion protein is mediated by the proximal AP-1 site of the MMP-9 promoter and correlates with reduced tumor cell invasion. Neoplasia 1999, 1, 368–372. [Google Scholar]
- Kajanne, R.; Miettinen, P.; Mehlem, A.; Leivonen, S.K.; Birrer, M.; Foschi, M.; Kähäri, V.M.; Leppä, S. EGF-R regulates MMP function in fibroblasts through MAPK and AP-1 pathways. J. Cell Physiol 2007, 212, 489–497. [Google Scholar]
- Dong, W.; Li, Y.; Gao, M.; Hu, M.; Li, X.; Mai, S.; Guo, N.; Yuan, S.; Song, L. IKKα contributes to UVB-induced VEGF expression by regulating AP-1 transactivation. Nucleic Acids Res 2012, 40, 2940–2955. [Google Scholar]
- Bae, S.K.; Bae, M.H.; Ahn, M.Y.; Son, M.J.; Lee, Y.M.; Bae, M.K.; Lee, O.H.; Park, B.C.; Kim, K.W. Egr-1 mediates transcriptional activation of IGF-II gene in response to hypoxia. Cancer Res 1999, 59, 5989–5994. [Google Scholar]
- Worden, B.; Yang, X.P.; Lee, T.L.; Bagain, L.; Yeh, N.T.; Cohen, J.G.; Van Waes, C.; Chen, Z. Hepatocyte growth factor/scatter factor differentially regulates expression of proangiogenic factors through Egr-1 in head and neck squamous cell carcinoma. Cancer Res 2005, 65, 7071–7080. [Google Scholar]
- Baron, V.; De Gregorio, G.; Krones-Herzig, A.; Virolle, T.; Calogero, A.; Urcis, R.; Mercola, D. Inhibition of Egr-1 expression reverses transformation of prostate cancer cells in vitro and in vivo. Oncogene 2003, 22, 4194–4204. [Google Scholar]
- Herath, N.I.; Boyd, A.W. The role of Eph receptors and ephrin ligands in colorectal cancer. Int. J. Cancer 2010, 126, 2003–2011. [Google Scholar]
- Biao-Xue, R.; Xi-Guang, C.; Shuan-ying, Y.; Wei, L.; Zong-juan, M. EphA2-dependent molecular targeting therapy for malignant tumors. Curr. Cancer Drug Targets 2011, 11, 1082–1097. [Google Scholar]
- Binda, E.; Visioli, A.; Giani, F.; Lamorte, G.; Copetti, M.; Pitter, K.L.; Huse, J.T.; Cajola, L.; Zanetti, N.; di Meco, F.; et al. The EphA2 receptor drives self-renewal and tumorigenicity in stem-like tumor-propagating cells from human glioblastomas. Cancer Cell 2012, 22, 765–780. [Google Scholar]
- Salaita, K.; Nair, P.M.; Petit, R.S.; Neve, R.M.; Das, D.; Gray, J.W.; Groves, J.T. Restriction of receptor movement alters cellular response: Physical force sensing by EphA2. Science 2010, 327, 1380–1385. [Google Scholar]
- Lee, J.W.; Han, H.D.; Shahzad, M.M.; Kim, S.W.; Mangala, L.S.; Nick, A.M.; Lu, C.; Langley, R.R.; Schmandt, R.; Kim, H.S.; et al. EphA2 immunoconjugate as molecularly targeted chemotherapy for ovarian carcinoma. J. Natl. Cancer Inst 2009, 101, 1193–1205. [Google Scholar]
- Miao, H.; Li, D.Q.; Mukherjee, A.; Guo, H.; Petty, A.; Cutter, J.; Basilion, J.P.; Sedor, J.; Wu, J.; Danielpour, D.; et al. EphA2 mediates ligand-dependent inhibition and ligand-independent promotion of cell migration and invasion via a reciprocal regulatory loop with Akt. Cancer Cell 2009, 16, 9–20. [Google Scholar]
- Jain, A.; Tindell, C.A.; Laux, I.; Hunter, J.B.; Curran, J.; Galkin, A.; Afar, D.E.; Aronson, N.; Shak, S.; Natale, R.B.; et al. Epithelial membrane protein-1 is a biomarker of gefitinib resistance. Proc. Natl. Acad. Sci. USA 2005, 102, 11858–11863. [Google Scholar]
- Karapetis, C.S.; Khambata-Ford, S.; Jonker, D.J.; O’Callaghan, C.J.; Tu, D.; Tebbutt, N.C.; Simes, R.J.; Chalchal, H.; Shapiro, J.D.; Robitaille, S.; et al. K-ras mutations and benefit from cetuximab in advanced colorectal cancer. N. Engl. J. Med 2008, 359, 1757–1765. [Google Scholar]
- Carrato, A.; Gómez, A.; Escudero, P.; Chaves, M.; Rivera, F.; Marcuello, E.; González, E.; Grávalos, C.; Constenla, M.; Manzano, J.L.; et al. Panitumumab and irinotecan every 3 weeks is an active and convenient regimen for second-line treatment of patients with wild-type K-RAS metastatic colorectal cancer. Clin. Transl. Oncol 2013, 15, 705–711. [Google Scholar]
- Harris, L.G.; Pannell, L.K.; Singh, S.; Samant, R.S.; Shevde, L.A. Increased vascularity and spontaneous metastasis of breast cancer by hedgehog signaling mediated upregulation of cyr61. Oncogene 2012, 31, 3370–3380. [Google Scholar]
- Haque, I.; De, A.; Majumder, M.; Mehta, S.; McGregor, D.; Banerjee, S.K.; van Veldhuizen, P.; Banerjee, S. The matricellular protein CCN1/Cyr61 is a critical regulator of Sonic Hedgehog in pancreatic carcinogenesis. J. Biol. Chem 2012, 287, 38569–38579. [Google Scholar]
- Barker, N.; van Es, J.H.; Kuipers, J.; Kujala, P.; van den Born, M.; Cozijnsen, M.; Haegebarth, A.; Korving, J.; Begthel, H.; Peters, P.J.; et al. Identification of stem cells in small intestine and colon by marker gene Lgr5. Nature 2007, 449, 1003–1007. [Google Scholar]
- Takahashi, H.; Ishii, H.; Nishida, N.; Takemasa, I.; Mizushima, T.; Ikeda, M.; Yokobori, T.; Mimori, K.; Yamamoto, H.; Sekimoto, M.; et al. Significance of Lgr5(+ve) cancer stem cells in the colon and rectum. Ann. Surg. Oncol 2011, 18, 1166–1174. [Google Scholar]
|Cancer Kinds||Histology||HOPX expression||DNA methylation||Prognostic relevance||References||Published year|
|Lung||SCC||Reduced in cancer||Not assessed||Not assessed||||2003|
|Adeno||Reduced in cancer||Not assessed||Yes||||2013|
|Placenta||Tropho||Reduced in cancer||Not assessed||Not assessed||||2003|
|Head and Neck||SCC||Reduced in cancer||Not assessed||Not assessed||||2004|
|Esophagus||SCC||Reduced in cancer||Cancer-prone||Yes||||2008|
|Uterine||Endo||Reduced in cancer||Cancer-prone||Not assessed||||2009|
|Stomach||Adeno||Reduced in cancer||Cancer-prone||Yes||||2010|
|Colon/Rectum||Adeno||Not assessed||Cancer-prone||Not assessed||||2011|
|Adeno||Reduced in cancer||Cancer-prone||Yes||||2012|
|Pancreas||Adeno||Reduced in cancer||Cancer-prone||No||||2012|
SCC, squamous cell carcinoma; Adeno, adenocarcinoma; Tropho, trophoblast; Endo, endometrial carcinoma.
|Cancer Kinds||In vivo tumorigenesis||In vitro tumorigenesis||Proliferaion||Apoptosis||Invasion||Angiogenesis||Mets in animial||Ref.||Published year|
|Placenta||Yes||Not assessed||Not assessed||Not assessed||Not assessed||Not assessed||Not assessed||||2003|
|Esophagus||Not assessed||Yes||Not assessed||Not assessed||Not assessed||Not assessed||Not assessed||||2008|
|Head and Neck||Not assessed||Yes||Not assessed||Not assessed||Not assessed||Not assessed||Not assessed||||2008|
|Lung||Yes||Yes||Yes||Not assessed||Not assessed||Not assessed||Not assessed||||2007|
|Not assessed||Not assessed||No||No||Yes||Not assessed||Yes||||2013|
|Uterine||Yes||Not assessed||Yes||Not assessed||Not assessed||Not assessed||Not assessed||||2009|
|Breast||Yes||Not assessed||Yes||Not assessed||Not assessed||Not assessed||Not assessed||||2009|
|Stomach||Not assessed||Yes||Yes||Yes||Yes||Not assessed||Not assessed||||2010|
|Pancreas||Not assessed||Yes||Yes||Yes||Yes||Not assessed||Not assessed||||2012|
SCC, squamous cell carcinoma; Adeno, adenocarcinoma; Tropho, trophoblast; Endo, endometrial carcinoma; Mets, metastasis.
© 2013 by the authors; licensee MDPI, Basel, Switzerland This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).