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TIN2对人胃上皮细胞系GES-1中端粒和染色体的影响。

Effects of TIN2 on telomeres and chromosomes in the human gastric epithelial cell line GES-1.

作者信息

Fu Fan, Hu Hua, Yang Shuai, Liang Xiaoqiu

机构信息

Cancer Research Institute, Key Laboratory of Tumor Cellular and Molecular Pathology, College of Hunan, University of South China, Hengyang, Hunan 421001, P.R. China.

Department of Pathology, The Fourth Hospital of Changsha, Changsha, Hunan 410006, P.R. China.

出版信息

Oncol Lett. 2018 Apr;15(4):5161-5166. doi: 10.3892/ol.2018.7927. Epub 2018 Feb 2.

DOI:10.3892/ol.2018.7927
PMID:29552152
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5840751/
Abstract

TERF1-interacting nuclear factor 2 (TIN2) is a key member of the protein complexes that protect telomeres. TIN2 contributes an important role in biological processes. In a previous study by the present authors, an association was reported between high TIN2 protein expression and gastric cancer. Therefore, it was hypothesized that abnormal TIN2 expression may cause the development of malignancies, including, gastric carcinomas. To investigate this hypothesis, the present study employed peptide nucleic acid fluorescence hybridization technology to analyze the human gastric epithelial GES-1 cells with high TIN2 expression or inhibited TIN2 expression. The results indicated that GES-1 cell lines with high TIN2 expression exhibited greater telomere dysfunction-induced damage compared with GES-1 cell lines with inhibited TIN2 expression. Chromosome analysis indicated that GES-1 cells with high TIN2 expression exhibited 2.48±1.30 aberrant chromosomal changes per 100 cells, that may contribute to telomere DNA damage. Therefore, aberrant chromosomal alterations may provide a novel perspective for the pathogenesis of gastric cancer.

摘要

端粒重复结合因子1相互作用核因子2(TIN2)是保护端粒的蛋白质复合物的关键成员。TIN2在生物过程中发挥着重要作用。在本作者之前的一项研究中,报道了TIN2蛋白高表达与胃癌之间的关联。因此,推测TIN2表达异常可能导致包括胃癌在内的恶性肿瘤的发生。为了验证这一假设,本研究采用肽核酸荧光杂交技术分析TIN2高表达或TIN2表达受抑制的人胃上皮GES-1细胞。结果表明,与TIN2表达受抑制的GES-1细胞系相比,TIN2高表达的GES-1细胞系表现出更大的端粒功能障碍诱导损伤。染色体分析表明,TIN2高表达的GES-1细胞每100个细胞表现出2.48±1.30个异常染色体变化,这可能导致端粒DNA损伤。因此,异常染色体改变可能为胃癌的发病机制提供一个新的视角。

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本文引用的文献

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Use of Fluorescence Quantitative Polymerase Chain Reaction (PCR) for the Detection of Escherichia coli Adhesion to Pig Intestinal Epithelial Cells.利用荧光定量聚合酶链反应(PCR)检测大肠杆菌对猪肠道上皮细胞的黏附
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Gene dosage reductions of Trf1 and/or Tin2 induce telomere DNA damage and lymphoma formation in aging mice.Trf1和/或Tin2的基因剂量降低会在衰老小鼠中诱导端粒DNA损伤和淋巴瘤形成。
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Binding of TPP1 protein to TIN2 protein is required for POT1a,b protein-mediated telomere protection.POT1a、b蛋白介导的端粒保护需要TPP1蛋白与TIN2蛋白结合。
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7
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Mol Cell Biol. 2014 Apr;34(7):1349-62. doi: 10.1128/MCB.01052-13. Epub 2014 Jan 27.
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A TIN2 dyskeratosis congenita mutation causes telomerase-independent telomere shortening in mice.TIN2 发育不良性角化不良突变导致小鼠端粒酶非依赖性端粒缩短。
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Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy.短端粒:从先天性角化不良到特发性再生障碍性贫血和恶性肿瘤。
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