نتایج جستجو برای: hypermethylated in cancer hic1

تعداد نتایج: 17198900  

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011

Ahmad Monabati, Mona Entezam, Mozhgan Rasti, Parastoo Tavasoli,

Background: Ras-associated domain family 1 (RASSF1A) and hypermethylated in cancer (HIC1) genes are methylated more frequently in breast cancer. Genetic factors that alter the DNA methylation levels in normal and tumor tissues could therefore influence the susceptibility to this tumor phenotype. Objective: We determined the frequency of aberrant methylation of HIC1 and RASSF1A gene promoters an...

Journal: :iranian biomedical journal 0
مژگان راستی mozhgan rasti پرستو توسلی parastoo tavasoli احمد منابتی ahmad monabati مونا انتظام mona entezam

background: ras-associated domain family 1 (rassf1a) and hypermethylated in cancer (hic1) genes are methylated more frequently in breast cancer. genetic factors that alter the dna methylation levels in normal and tumor tissues could therefore influence the susceptibility to this tumor phenotype. objective: we determined the frequency of aberrant methylation of hic1 and rassf1a gene promoters an...

Journal: :Molecular cancer research : MCR 2009
Mathias Jenal Emmanuelle Trinh Christian Britschgi Adrian Britschgi Vincent Roh Stephan A Vorburger Andreas Tobler Dominique Leprince Martin F Fey Kristian Helin Mario P Tschan

The Hypermethylated in Cancer 1 (HIC1) gene encodes a zinc finger transcriptional repressor that cooperates with p53 to suppress cancer development. We and others recently showed that HIC1 is a transcriptional target of p53. To identify additional transcriptional regulators of HIC1, we screened a set of transcription factors for regulation of a human HIC1 promoter reporter. We found that E2F1 s...

Journal: :Cell 2005
Wen Yong Chen David H. Wang RayWhay Chiu Yen Jianyuan Luo Wei Gu Stephen B. Baylin

Hypermethylated in cancer 1 (HIC1) is an epigenetically regulated transcriptional repressor that functionally cooperates with p53 to suppress age-dependent development of cancer in mice. Here we show that the mechanism by which the loss of HIC1 function promotes tumorigenesis is via activating the stress-controlling protein SIRT1 and thereby attenuating p53 function. HIC1 forms a transcriptiona...

2016
Lucie Janeckova Michal Kolar Jiri Svec Lucie Lanikova Vendula Pospichalova Nikol Baloghova Martina Vojtechova Eva Sloncova Hynek Strnad Vladimir Korinek

Neoplastic growth is frequently associated with genomic DNA methylation that causes transcriptional silencing of tumor suppressor genes. We used a collection of colorectal polyps and carcinomas in combination with bioinformatics analysis of large datasets to study the expression and methylation of Hypermethylated in cancer 1 (HIC1), a tumor suppressor gene inactivated in many neoplasms. In prem...

Journal: :Cancer research 2008
Kimberly J Briggs Charles G Eberhart D Neil Watkins

Hypermethylated in cancer-1 (HIC1) is a tumor suppressor frequently targeted for promoter hypermethylation in medulloblastoma, an embryonal tumor of the cerebellum. Recently, we showed that HIC1 is a direct transcriptional repressor of ATOH1, a proneural transcription factor required for normal cerebellar development, as well as for medulloblastoma cell viability. Because demethylating agents c...

Journal: :Journal of Immunology 2023

Abstract The group 1 innate lymphoid cell compartment is comprised of conventional natural killer (cNK) and type cells (ILC1). Within the pool, these are delineated by expression transcription factor TBET, both subtypes express surface receptors NK1.1 NKp46. Functionally, ILC1 cNK have been shown to mediate pathogen clearance tumour control through release cytokines, particularly IFN-□. While b...

2016
Wenyi Wu Liting Zhang Jianqing Lin Hanwei Huang Bai Shi Xingong Lin Zhongxin Huang Chaoyang Wang Jianlong Qiu Xiaolong Wei

Hypermethylation leading to the loss of hypermethylated in cancer-1 (HIC1) gene expression occurs in many different types of human cancer. HIC1 is a transcriptional repressor that directly binds to the promoter region of NAD-dependent deacetylase sirtuin-1 (SIRT1). SIRT1 functions in cell growth, is anti-apoptotic, protect neurons, functions in senescence, and regulates energy restriction. Epig...

Journal: :The International Journal of Biochemistry & Cell Biology 2009

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید