Cancer specific promoter CpG Islands hypermethylation of HOP homeobox (HOPX) gene and its potential tumor suppressive role in pancreatic carcinogenesis

<p>Abstract</p> <p>Background</p> <p>We have recently identified HOP hoemobox (HOPX) as a tumor suppressor gene candidate, characterized by tumor-specific promoter DNA hypermethylation in human cancers, and it can remarkably inhibit tumors’ aggressive phenotypes. In thi...

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Main Authors: Waraya Mina, Yamashita Keishi, Katoh Hiroshi, Ooki Akira, Kawamata Hiroshi, Nishimiya Hiroshi, Nakamura Kazunori, Ema Akira, Watanabe Masahiko
Format: Article
Language:English
Published: BMC 2012-09-01
Series:BMC Cancer
Subjects:
Online Access:http://www.biomedcentral.com/1471-2407/12/397
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author Waraya Mina
Yamashita Keishi
Katoh Hiroshi
Ooki Akira
Kawamata Hiroshi
Nishimiya Hiroshi
Nakamura Kazunori
Ema Akira
Watanabe Masahiko
author_facet Waraya Mina
Yamashita Keishi
Katoh Hiroshi
Ooki Akira
Kawamata Hiroshi
Nishimiya Hiroshi
Nakamura Kazunori
Ema Akira
Watanabe Masahiko
author_sort Waraya Mina
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>We have recently identified HOP hoemobox (HOPX) as a tumor suppressor gene candidate, characterized by tumor-specific promoter DNA hypermethylation in human cancers, and it can remarkably inhibit tumors’ aggressive phenotypes. In this current study, we for the first time examined methylation level of HOPX and tested the functional relevance in pancreatic cancer (PC).</p> <p>Methods</p> <p>Clinical features of HOPX promoter hypermethylation was investigated in 89 PC tissues, and immunohistochemistry was added. We also examined its functional relevance in phenotype assays such as soft agar, proliferation, invasion, and cell cycle analysis.</p> <p>Results</p> <p>PC tissues had HOPX gene hypermethylation as compared to the corresponding normal pancreas tissues, and its uniqueness was robust to discriminate tumor from normal tissues (AUC = 0.85, P < 0.0001). Unexpectedly, HOPX was increased in expression in tumor tissues, and immunohistochemistry revealed its predominant expression in the Langerhans islet cells, where HOPX was reduced in expression for PC cells with promoter hypermethylation. HOPX transfectants exhibited G1 arrest with subG1 accumulation, and inhibited tumor forming and invasive ability.</p> <p>Conclusion</p> <p>Defective expression of HOPX which is consistent with promoter DNA hypermethylation may explain aggressive phenotype of pancreatic cancer, and intense expression of HOPX in the Langerhans cells may in turn uniquely contribute to pancreatic carcinogenesis.</p>
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spelling doaj.art-ae473bb549584c5aba73fd557075e0b92022-12-22T03:04:39ZengBMCBMC Cancer1471-24072012-09-0112139710.1186/1471-2407-12-397Cancer specific promoter CpG Islands hypermethylation of HOP homeobox (HOPX) gene and its potential tumor suppressive role in pancreatic carcinogenesisWaraya MinaYamashita KeishiKatoh HiroshiOoki AkiraKawamata HiroshiNishimiya HiroshiNakamura KazunoriEma AkiraWatanabe Masahiko<p>Abstract</p> <p>Background</p> <p>We have recently identified HOP hoemobox (HOPX) as a tumor suppressor gene candidate, characterized by tumor-specific promoter DNA hypermethylation in human cancers, and it can remarkably inhibit tumors’ aggressive phenotypes. In this current study, we for the first time examined methylation level of HOPX and tested the functional relevance in pancreatic cancer (PC).</p> <p>Methods</p> <p>Clinical features of HOPX promoter hypermethylation was investigated in 89 PC tissues, and immunohistochemistry was added. We also examined its functional relevance in phenotype assays such as soft agar, proliferation, invasion, and cell cycle analysis.</p> <p>Results</p> <p>PC tissues had HOPX gene hypermethylation as compared to the corresponding normal pancreas tissues, and its uniqueness was robust to discriminate tumor from normal tissues (AUC = 0.85, P < 0.0001). Unexpectedly, HOPX was increased in expression in tumor tissues, and immunohistochemistry revealed its predominant expression in the Langerhans islet cells, where HOPX was reduced in expression for PC cells with promoter hypermethylation. HOPX transfectants exhibited G1 arrest with subG1 accumulation, and inhibited tumor forming and invasive ability.</p> <p>Conclusion</p> <p>Defective expression of HOPX which is consistent with promoter DNA hypermethylation may explain aggressive phenotype of pancreatic cancer, and intense expression of HOPX in the Langerhans cells may in turn uniquely contribute to pancreatic carcinogenesis.</p>http://www.biomedcentral.com/1471-2407/12/397HOP homeoboxPancreatic cancerMethylation
spellingShingle Waraya Mina
Yamashita Keishi
Katoh Hiroshi
Ooki Akira
Kawamata Hiroshi
Nishimiya Hiroshi
Nakamura Kazunori
Ema Akira
Watanabe Masahiko
Cancer specific promoter CpG Islands hypermethylation of HOP homeobox (HOPX) gene and its potential tumor suppressive role in pancreatic carcinogenesis
BMC Cancer
HOP homeobox
Pancreatic cancer
Methylation
title Cancer specific promoter CpG Islands hypermethylation of HOP homeobox (HOPX) gene and its potential tumor suppressive role in pancreatic carcinogenesis
title_full Cancer specific promoter CpG Islands hypermethylation of HOP homeobox (HOPX) gene and its potential tumor suppressive role in pancreatic carcinogenesis
title_fullStr Cancer specific promoter CpG Islands hypermethylation of HOP homeobox (HOPX) gene and its potential tumor suppressive role in pancreatic carcinogenesis
title_full_unstemmed Cancer specific promoter CpG Islands hypermethylation of HOP homeobox (HOPX) gene and its potential tumor suppressive role in pancreatic carcinogenesis
title_short Cancer specific promoter CpG Islands hypermethylation of HOP homeobox (HOPX) gene and its potential tumor suppressive role in pancreatic carcinogenesis
title_sort cancer specific promoter cpg islands hypermethylation of hop homeobox hopx gene and its potential tumor suppressive role in pancreatic carcinogenesis
topic HOP homeobox
Pancreatic cancer
Methylation
url http://www.biomedcentral.com/1471-2407/12/397
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