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The H3K9 methyltransferase G9a is a marker of aggressive ovarian cancer that promotes peritoneal metastasis
BACKGROUND: Ovarian cancer (OCa) peritoneal metastasis is the leading cause of cancer–related deaths in women with limited therapeutic options available for treating it and poor prognosis, as the underlying mechanism is not fully understood. METHOD: The clinicopathological correlation of G9a express...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4260797/ https://www.ncbi.nlm.nih.gov/pubmed/25115793 http://dx.doi.org/10.1186/1476-4598-13-189 |
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author | Hua, Kuo-Tai Wang, Ming-Yang Chen, Min-Wei Wei, Lin-Hung Chen, Chi-Kuan Ko, Ching-Huai Jeng, Yung-Ming Sung, Pi-Lin Jan, Yi-Hua Hsiao, Michael Kuo, Min-Liang Yen, Men-Luh |
author_facet | Hua, Kuo-Tai Wang, Ming-Yang Chen, Min-Wei Wei, Lin-Hung Chen, Chi-Kuan Ko, Ching-Huai Jeng, Yung-Ming Sung, Pi-Lin Jan, Yi-Hua Hsiao, Michael Kuo, Min-Liang Yen, Men-Luh |
author_sort | Hua, Kuo-Tai |
collection | PubMed |
description | BACKGROUND: Ovarian cancer (OCa) peritoneal metastasis is the leading cause of cancer–related deaths in women with limited therapeutic options available for treating it and poor prognosis, as the underlying mechanism is not fully understood. METHOD: The clinicopathological correlation of G9a expression was assessed in tumor specimens of ovarian cancer patients. Knockdown or overexpression of G9a in ovarian cancer cell lines was analysed with regard to its effect on adhesion, migration, invasion and anoikis-resistance. In vivo biological functions of G9a were tested by i.p. xenograft ovarian cancer models. Microarray and quantitative RT-PCR were used to analyze G9a-regulated downstream target genes. RESULTS: We found that the expression of histone methyltransferase G9a was highly correlated with late stage, high grade, and serous-type OCa. Higher G9a expression predicted a shorter survival in ovarian cancer patients. Furthermore, G9a expression was higher in metastatic lesions compared with their corresponding ovarian primary tumors. Knockdown of G9a expression suppressed prometastatic cellular activities including adhesion, migration, invasion and anoikis-resistance of ovarian cancer cell lines, while G9a over-expression promoted these cellular properties. G9a depletion significantly attenuated the development of ascites and tumor nodules in a peritoneal dissemination model. Importantly, microarray and quantitative RT-PCR analysis revealed that G9a regulates a cohort of tumor suppressor genes including CDH1, DUSP5, SPRY4, and PPP1R15A in ovarian cancer. Expression of these genes was also inversely correlated with G9a expression in OCa specimens. CONCLUSION: We propose that G9a contributes to multiple steps of ovarian cancer metastasis and represents a novel target to combat this deadly disease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1476-4598-13-189) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4260797 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42607972014-12-10 The H3K9 methyltransferase G9a is a marker of aggressive ovarian cancer that promotes peritoneal metastasis Hua, Kuo-Tai Wang, Ming-Yang Chen, Min-Wei Wei, Lin-Hung Chen, Chi-Kuan Ko, Ching-Huai Jeng, Yung-Ming Sung, Pi-Lin Jan, Yi-Hua Hsiao, Michael Kuo, Min-Liang Yen, Men-Luh Mol Cancer Research BACKGROUND: Ovarian cancer (OCa) peritoneal metastasis is the leading cause of cancer–related deaths in women with limited therapeutic options available for treating it and poor prognosis, as the underlying mechanism is not fully understood. METHOD: The clinicopathological correlation of G9a expression was assessed in tumor specimens of ovarian cancer patients. Knockdown or overexpression of G9a in ovarian cancer cell lines was analysed with regard to its effect on adhesion, migration, invasion and anoikis-resistance. In vivo biological functions of G9a were tested by i.p. xenograft ovarian cancer models. Microarray and quantitative RT-PCR were used to analyze G9a-regulated downstream target genes. RESULTS: We found that the expression of histone methyltransferase G9a was highly correlated with late stage, high grade, and serous-type OCa. Higher G9a expression predicted a shorter survival in ovarian cancer patients. Furthermore, G9a expression was higher in metastatic lesions compared with their corresponding ovarian primary tumors. Knockdown of G9a expression suppressed prometastatic cellular activities including adhesion, migration, invasion and anoikis-resistance of ovarian cancer cell lines, while G9a over-expression promoted these cellular properties. G9a depletion significantly attenuated the development of ascites and tumor nodules in a peritoneal dissemination model. Importantly, microarray and quantitative RT-PCR analysis revealed that G9a regulates a cohort of tumor suppressor genes including CDH1, DUSP5, SPRY4, and PPP1R15A in ovarian cancer. Expression of these genes was also inversely correlated with G9a expression in OCa specimens. CONCLUSION: We propose that G9a contributes to multiple steps of ovarian cancer metastasis and represents a novel target to combat this deadly disease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1476-4598-13-189) contains supplementary material, which is available to authorized users. BioMed Central 2014-08-12 /pmc/articles/PMC4260797/ /pubmed/25115793 http://dx.doi.org/10.1186/1476-4598-13-189 Text en © Hua et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Hua, Kuo-Tai Wang, Ming-Yang Chen, Min-Wei Wei, Lin-Hung Chen, Chi-Kuan Ko, Ching-Huai Jeng, Yung-Ming Sung, Pi-Lin Jan, Yi-Hua Hsiao, Michael Kuo, Min-Liang Yen, Men-Luh The H3K9 methyltransferase G9a is a marker of aggressive ovarian cancer that promotes peritoneal metastasis |
title | The H3K9 methyltransferase G9a is a marker of aggressive ovarian cancer that promotes peritoneal metastasis |
title_full | The H3K9 methyltransferase G9a is a marker of aggressive ovarian cancer that promotes peritoneal metastasis |
title_fullStr | The H3K9 methyltransferase G9a is a marker of aggressive ovarian cancer that promotes peritoneal metastasis |
title_full_unstemmed | The H3K9 methyltransferase G9a is a marker of aggressive ovarian cancer that promotes peritoneal metastasis |
title_short | The H3K9 methyltransferase G9a is a marker of aggressive ovarian cancer that promotes peritoneal metastasis |
title_sort | h3k9 methyltransferase g9a is a marker of aggressive ovarian cancer that promotes peritoneal metastasis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4260797/ https://www.ncbi.nlm.nih.gov/pubmed/25115793 http://dx.doi.org/10.1186/1476-4598-13-189 |
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