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Promoter methylation of tumor suppressor genes in esophageal squamous cell carcinoma

Esophageal squamous cell carcinoma (ESCC) is a prevalent and fatal cancer in China and other Asian countries. Epigenetic silencing of key tumor suppressor genes (TSGs) is critical to ESCC initiation and progression. Recently, many novel TSGs silenced by promoter methylation have been identified in E...

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Autores principales: Li, Ji-Sheng, Ying, Jian-Ming, Wang, Xiu-Wen, Wang, Zhao-Hui, Tao, Qian, Li, Li-Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sun Yat-sen University Cancer Center 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3845589/
https://www.ncbi.nlm.nih.gov/pubmed/22572016
http://dx.doi.org/10.5732/cjc.011.10381
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author Li, Ji-Sheng
Ying, Jian-Ming
Wang, Xiu-Wen
Wang, Zhao-Hui
Tao, Qian
Li, Li-Li
author_facet Li, Ji-Sheng
Ying, Jian-Ming
Wang, Xiu-Wen
Wang, Zhao-Hui
Tao, Qian
Li, Li-Li
author_sort Li, Ji-Sheng
collection PubMed
description Esophageal squamous cell carcinoma (ESCC) is a prevalent and fatal cancer in China and other Asian countries. Epigenetic silencing of key tumor suppressor genes (TSGs) is critical to ESCC initiation and progression. Recently, many novel TSGs silenced by promoter methylation have been identified in ESCC, and these genes further serve as potential tumor markers for high-risk group stratification, early detection, and prognosis prediction. This review summarizes recent discoveries on aberrant promoter methylation of TSGs in ESCC, providing better understanding of the role of disrupted epigenetic regulation in tumorigenesis and insight into diagnostic and prognostic biomarkers for this malignancy.
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spelling pubmed-38455892013-12-11 Promoter methylation of tumor suppressor genes in esophageal squamous cell carcinoma Li, Ji-Sheng Ying, Jian-Ming Wang, Xiu-Wen Wang, Zhao-Hui Tao, Qian Li, Li-Li Chin J Cancer Review Esophageal squamous cell carcinoma (ESCC) is a prevalent and fatal cancer in China and other Asian countries. Epigenetic silencing of key tumor suppressor genes (TSGs) is critical to ESCC initiation and progression. Recently, many novel TSGs silenced by promoter methylation have been identified in ESCC, and these genes further serve as potential tumor markers for high-risk group stratification, early detection, and prognosis prediction. This review summarizes recent discoveries on aberrant promoter methylation of TSGs in ESCC, providing better understanding of the role of disrupted epigenetic regulation in tumorigenesis and insight into diagnostic and prognostic biomarkers for this malignancy. Sun Yat-sen University Cancer Center 2013-01 /pmc/articles/PMC3845589/ /pubmed/22572016 http://dx.doi.org/10.5732/cjc.011.10381 Text en Chinese Journal of Cancer http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission.
spellingShingle Review
Li, Ji-Sheng
Ying, Jian-Ming
Wang, Xiu-Wen
Wang, Zhao-Hui
Tao, Qian
Li, Li-Li
Promoter methylation of tumor suppressor genes in esophageal squamous cell carcinoma
title Promoter methylation of tumor suppressor genes in esophageal squamous cell carcinoma
title_full Promoter methylation of tumor suppressor genes in esophageal squamous cell carcinoma
title_fullStr Promoter methylation of tumor suppressor genes in esophageal squamous cell carcinoma
title_full_unstemmed Promoter methylation of tumor suppressor genes in esophageal squamous cell carcinoma
title_short Promoter methylation of tumor suppressor genes in esophageal squamous cell carcinoma
title_sort promoter methylation of tumor suppressor genes in esophageal squamous cell carcinoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3845589/
https://www.ncbi.nlm.nih.gov/pubmed/22572016
http://dx.doi.org/10.5732/cjc.011.10381
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