نتایج جستجو برای: runx3 ecad

تعداد نتایج: 857  

Journal: :Blood 2008
Chi Keung Cheng Libby Li Suk Hang Cheng Kin Mang Lau Natalie P H Chan Raymond S M Wong Matthew M K Shing Chi Kong Li Margaret H L Ng

RUNX3/AML2 is a Runt domain transcription factor like RUNX1/AML1 and RUNX2/AML3. Regulated by 2 promoters P1 and P2, RUNX3 is frequently inactivated by P2 methylation in solid tumors. Growing evidence has suggested a role of this transcription factor in hematopoiesis. However, genetic alterations have not been reported in blood cancers. In this study on 73 acute myeloid leukemia (AML) patients ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2004
Ori Brenner Ditsa Levanon Varda Negreanu Olga Golubkov Ofer Fainaru Eilon Woolf Yoram Groner

RUNX transcription factors are key regulators of lineage-specific gene expression and might be involved in autoimmune diseases. Runx3 plays a role during the development of sensory neurons and T cells and regulates transforming growth factor beta (TGF-beta) signaling in dendritic cells. Here, we report that at 4 weeks of age, Runx3 knockout (KO) mice spontaneously develop inflammatory bowel dis...

2018
Karolin Heinze Daniel Kritsch Alexander S Mosig Matthias Dürst Norman Häfner Ingo B Runnebaum

(1) Background: Epithelial ovarian cancer (EOC) is the most lethal cancer of the female reproductive system. In an earlier study, we identified multiple genes as hypermethylated in tumors of patients with poor prognosis. The most promising combination of markers to predict a patient's outcome was CaMKIINα and RUNX3. Aim of this study was to functionally validate the importance of both genes. (2...

Journal: :The Journal of biological chemistry 2007
Ken-ichi Inoue Kosei Ito Motomi Osato Bernett Lee Suk-Chul Bae Yoshiaki Ito

Runx3, a Runt domain transcription factor, determines neurotrophin receptor phenotype in dorsal root ganglion (DRG) neurons. Molecular mechanisms by which Runx3 controls distinct neurotrophin receptors are largely unknown. Here, we show that RUNX3 abolished mRNA induction of TRKB expression, and concomitantly altered the neurotrophin response in a differentiating neuroblastoma cell line. In con...

Journal: :Asian Pacific journal of cancer prevention : APJCP 2009
Somkid Dachrut S Banthaisong M Sripa A Paeyao C Ho S A Lee C Kosinski M A Patil J Zhang X Chen Banchob Sripa Chawalit Pairojkul

Runt-related transcription factor 3 (RUNX3) is a candidate tumor suppressor gene, localized on 1p36, involved in TGF-beta-Smads signaling. To assess its role in liver fluke-associated intrahepatic cholangiocarcinoma (ICC), the promoter methylation status was investigated in 53 ICCs by methylation-specific PCR, with determination of loss of 1p36.1 by microarray comparative genomic hybridization ...

Journal: :Mechanisms of Development 2001
Ditsa Levanon Ori Brenner Varda Negreanu David Bettoun Eilon Woolf Raya Eilam Joseph Lotem Uri Gat Florian Otto Nancy Speck Yoram Groner

The human RUNX3/AML2 gene belongs to the 'runt domain' family of transcription factors that act as gene expression regulators in major developmental pathways. Here, we describe the expression pattern of Runx3 during mouse embryogenesis compared to the expression pattern of Runx1. E10.5 and E14.5-E16.5 embryos were analyzed using both immunohistochemistry and beta-galactosidase activity of targe...

Journal: :Journal of immunology 2012
Duy Pham Joshua W Vincentz Anthony B Firulli Mark H Kaplan

A transcription factor network that includes STAT4, T-bet, and Runx3 promotes the differentiation of Th1 cells and inflammatory immune responses. How additional transcription factors regulate the function of Th1 cells has not been defined. In this study we show that the negative regulatory factor Twist1 decreases expression of T-bet, Runx3, and IL-12Rβ2 as it inhibits IFN-γ production. Ectopic ...

2018
Matteo Vecellio Adrian Cortes Amity R Roberts Jonathan Ellis Carla Jayne Cohen Julian C Knight Matthew A Brown Paul Bowness Bryan Paul Wordsworth

Objectives To explore the functions of RUNX3 single nucleotide polymorphisms (SNPs) associated with ankylosing spondylitis (AS). Methods Individual SNP associations were evaluated in 4230 UK cases. Their effects on transcription factor (TF) binding, transcription regulation, chromatin modifications, gene expression and gene interactions were tested by database interrogation, luciferase report...

2015
Yuting Zhu Jianhua Fu Haiping Yang Yuqing Pan Li Yao Xindong Xue

BACKGROUND Bronchopulmonary dysplasia (BPD) in premature infants is a predominantly secondary occurrence to intrauterine inflammation/infection and postpartum mechanical ventilation; in recent years, an association with epigenetics has also been found. DNA methylation, catalyzed by DNA methyl transferases (DNMTs), and tri-methylation of lysine 27 on histone H3 (H3K27me3), mediated by the methyl...

Journal: :Oncology reports 2007
Sing-Huang Tan Hiroshi Ida Quek-Choon Lau Boon-Cher Goh Wei-Shieng Chieng Marie Loh Yoshiaki Ito

The purpose was to validate the use of RUNX3 as a potential biomarker for detection of cancer in serum samples and to determine its sensitivity alone and in combination with p16, RASSF1A and CDH1 using methylation-specific polymerase chain reaction (MSP). We examined the promoter methylation status of RUNX3, p16, RASSF1A and CDH1 by MSP using the serum of 70 metastatic breast, non-small cell lu...

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