Reduced Expression and Aberrant Splicing of ING4 in Human Stomach Adencarcinoma

来源 :第八次全国医学遗传学学术会议(中华医学会2009年医学遗传学年会) | 被引量 : 0次 | 上传用户:wgp121554715
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
  As a member of ING gene family which harbor the PHD domain and NLS domain, ING4 was reported to interact with tumor suppressor p53 and found to be involved in various biological activities, including cell cycle arrest, regulation of gene transcription, DNA repair and apoptosis.ING4_vl was located in nucleus whereas other three variants were located in cytoplasm.To clarify the role of ING4 in human stomach adencarcinoma, we first compared ING4 expression in four human gastric adenocarcinoma cell lines by RT-PCR and Real-time PCR.Low ING4 mRNA level was found in all cell lines, while there was lower ING4 expression found in poorly differentiated cell lines.
其他文献
会议
Background Toll like receptor 4 (TLR4), a member of the pathogen recognition receptors (PRR), has been shown to be implicated in atherosclerotic pathogenesis.But its precise mechanism remains unclear.
Background Recent reports suggest that GAG triplet expansions of spinocerebellar ataxia type 2 and 3 (SCA2 and SCA3/MJD) genes (ATXN2 and MJD1) are the cause of typical levodopa-responsive Parkinson s
会议
Background The SPINK5 gene was found to be responsible for Netherton syndrome, a rare recessive skin disease that is accompanied by severe atopic manifestations including atopic dermatitis, allergic r
Objective Chronic hepatitis B virus (HBV) infection is the most common cause of hepatic fibrosis and hepatocellular carcinoma (HCC).Chronic hepatitis B (CHB) appears to progress more rapidly in males
The aim of this study was to investigate the association of single nucleotide polymorphisms (SNPs) in tissue non-specific alkaline phosphatase (TNAP) with ankylosing spondylitis (AS) in the Chinese Ha
Background Genetic variations of the human RETN gene are associated with metabolic phenotypes, including obesity, insulin sensitivity, diabetes and coronary heart disease.There are few studies of two
Suicidal behavior (SB) as a serious public health problem is partly heritable.Identifying the genes and the neurobiologic pathways relevant to suicidal behavior is important for preventative strategie
会议
In order to explore the different genetic background of non-obese and obese type 2 diabetes, we tried to genotype six SNPs (-11391G/A,-11377C/G,-10068G/A, G54V,Y111H and 4545G/C) inthe adipose most ab
5-HT2C, a serotonin (5-hydroxytryptamine, 5-HT) receptor, has been the subject of considerable research because of its high affinity for risperidone, an effective first-line atypical neurolepic drug.R
会议