نتایج جستجو برای: hypermethylated in cancer hic1

تعداد نتایج: 17198900  

Journal: :Science translational medicine 2013
Martin J Aryee Wennuan Liu Julia C Engelmann Philipp Nuhn Meltem Gurel Michael C Haffner David Esopi Rafael A Irizarry Robert H Getzenberg William G Nelson Jun Luo Jianfeng Xu William B Isaacs G Steven Bova Srinivasan Yegnasubramanian

Human cancers almost ubiquitously harbor epigenetic alterations. Although such alterations in epigenetic marks, including DNA methylation, are potentially heritable, they can also be dynamically altered. Given this potential for plasticity, the degree to which epigenetic changes can be subject to selection and act as drivers of neoplasia has been questioned. We carried out genome-scale analyses...

Journal: :Journal of the National Cancer Institute 2013
Lina Sun He Li Junliang Chen Vanessa Dehennaut Yuhao Zhao Yuyu Yang Yasumasa Iwasaki Brigitte Kahn-Perles Dominique Leprince Qi Chen Aiguo Shen Yong Xu

BACKGROUND Epithelial-to-mesenchymal transition (EMT) plays a pivotal role in lung cancer metastasis. The class III deacetylase sirtuin 1 (SIRT1) possesses both pro- and anticarcinogenic properties. The role of SIRT1 in lung cancer EMT is largely undefined. METHODS The effect of SIRT1 on migration of lung cancer cells was evaluated by wound healing assay in vitro and metastasis assay in nude ...

Journal: :PLoS Genetics 2006
Kevin Pruitt Rebekah L Zinn Joyce E Ohm Kelly M McGarvey Sung-Hae L Kang D. Neil Watkins James G Herman Stephen B Baylin

The class III histone deactylase (HDAC), SIRT1, has cancer relevance because it regulates lifespan in multiple organisms, down-regulates p53 function through deacetylation, and is linked to polycomb gene silencing in Drosophila. However, it has not been reported to mediate heterochromatin formation or heritable silencing for endogenous mammalian genes. Herein, we show that SIRT1 localizes to pr...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2011
Audrey Vincent Noriyuki Omura Seung-Mo Hong Andrew Jaffe James Eshleman Michael Goggins

PURPOSE The goal of this study was to comprehensively identify CpG island methylation alterations between pancreatic cancers and normal pancreata and their associated gene expression alterations. EXPERIMENTAL DESIGN We employed methylated CpG island amplification followed by CpG island microarray, a method previously validated for its accuracy and reproducibility, to analyze the methylation p...

Journal: :Human molecular genetics 1999
T H Huang M R Perry D E Laux

CpG island hypermethylation is known to be associated with gene silencing in cancer. This epigenetic event is generally accepted as a stochastic process in tumor cells resulting from aberrant DNA methyltransferase (DNA-MTase) activities. Specific patterns of CpG island methylation could result from clonal selection of cells having growth advantages due to silencing of associated tumor suppresso...

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