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ARID2: A new tumor suppressor gene in hepatocellular carcinoma

Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide, however, genetic-environmental interactions and mechanisms associated with the development of HCC remains largely unclear. Our recent work described novel inactivating mutations of ARID2 (AT-rich interactive domain 2) i...

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Autores principales: Zhao, Hong, Wang, Jian, Han, Yongqing, Huang, Zhen, Ying, Jianming, Bi, Xinyu, Zhao, Jianjun, Fang, Yi, Zhou, Haitao, Zhou, Jianguo, Li, Zhiyu, Zhang, Yefan, Yang, Xue, Yan, Tao, Wang, Linfang, Torbenson, Michael S., Cai, Jianqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3259997/
https://www.ncbi.nlm.nih.gov/pubmed/22095441
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author Zhao, Hong
Wang, Jian
Han, Yongqing
Huang, Zhen
Ying, Jianming
Bi, Xinyu
Zhao, Jianjun
Fang, Yi
Zhou, Haitao
Zhou, Jianguo
Li, Zhiyu
Zhang, Yefan
Yang, Xue
Yan, Tao
Wang, Linfang
Torbenson, Michael S.
Cai, Jianqiang
author_facet Zhao, Hong
Wang, Jian
Han, Yongqing
Huang, Zhen
Ying, Jianming
Bi, Xinyu
Zhao, Jianjun
Fang, Yi
Zhou, Haitao
Zhou, Jianguo
Li, Zhiyu
Zhang, Yefan
Yang, Xue
Yan, Tao
Wang, Linfang
Torbenson, Michael S.
Cai, Jianqiang
author_sort Zhao, Hong
collection PubMed
description Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide, however, genetic-environmental interactions and mechanisms associated with the development of HCC remains largely unclear. Our recent work described novel inactivating mutations of ARID2 (AT-rich interactive domain 2) in four major subtypes of HCC through exomic sequencing of ten HCV-associated HCCs and subsequent evaluation of the tumors from additional affected individuals. Here, we summarize the current knowledge about the relevance of ARID2 in HCC and the implication in future patient care.
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spelling pubmed-32599972012-01-18 ARID2: A new tumor suppressor gene in hepatocellular carcinoma Zhao, Hong Wang, Jian Han, Yongqing Huang, Zhen Ying, Jianming Bi, Xinyu Zhao, Jianjun Fang, Yi Zhou, Haitao Zhou, Jianguo Li, Zhiyu Zhang, Yefan Yang, Xue Yan, Tao Wang, Linfang Torbenson, Michael S. Cai, Jianqiang Oncotarget Research Perspectives Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide, however, genetic-environmental interactions and mechanisms associated with the development of HCC remains largely unclear. Our recent work described novel inactivating mutations of ARID2 (AT-rich interactive domain 2) in four major subtypes of HCC through exomic sequencing of ten HCV-associated HCCs and subsequent evaluation of the tumors from additional affected individuals. Here, we summarize the current knowledge about the relevance of ARID2 in HCC and the implication in future patient care. Impact Journals LLC 2011-11-16 /pmc/articles/PMC3259997/ /pubmed/22095441 Text en Copyright: © 2011 Zhao et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
spellingShingle Research Perspectives
Zhao, Hong
Wang, Jian
Han, Yongqing
Huang, Zhen
Ying, Jianming
Bi, Xinyu
Zhao, Jianjun
Fang, Yi
Zhou, Haitao
Zhou, Jianguo
Li, Zhiyu
Zhang, Yefan
Yang, Xue
Yan, Tao
Wang, Linfang
Torbenson, Michael S.
Cai, Jianqiang
ARID2: A new tumor suppressor gene in hepatocellular carcinoma
title ARID2: A new tumor suppressor gene in hepatocellular carcinoma
title_full ARID2: A new tumor suppressor gene in hepatocellular carcinoma
title_fullStr ARID2: A new tumor suppressor gene in hepatocellular carcinoma
title_full_unstemmed ARID2: A new tumor suppressor gene in hepatocellular carcinoma
title_short ARID2: A new tumor suppressor gene in hepatocellular carcinoma
title_sort arid2: a new tumor suppressor gene in hepatocellular carcinoma
topic Research Perspectives
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3259997/
https://www.ncbi.nlm.nih.gov/pubmed/22095441
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