首页> 美国卫生研究院文献>BMC Molecular Biology >Matrix association region/scaffold attachment region (MAR/SAR) sequence: its vital role in mediating chromosome breakages in nasopharyngeal epithelial cells via oxidative stress-induced apoptosis
【2h】

Matrix association region/scaffold attachment region (MAR/SAR) sequence: its vital role in mediating chromosome breakages in nasopharyngeal epithelial cells via oxidative stress-induced apoptosis

机译:基质缔合区/支架附着区(MAR / SAR)序列:在氧化应激诱导的凋亡中介导鼻咽上皮细胞染色体断裂中的重要作用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

BackgroundOxidative stress is known to be involved in most of the aetiological factors of nasopharyngeal carcinoma (NPC). Cells that are under oxidative stress may undergo apoptosis. We have previously demonstrated that oxidative stress-induced apoptosis could be a potential mechanism mediating chromosome breakages in nasopharyngeal epithelial cells. Additionally, caspase-activated DNase (CAD) may be the vital player in mediating the chromosomal breakages during oxidative stress-induced apoptosis. Chromosomal breakage occurs during apoptosis and chromosome rearrangement. Chromosomal breakages tend to cluster in certain regions, such as matrix association region/scaffold attachment region (MAR/SAR). We hypothesised that oxidative stress-induced apoptosis may result in chromosome breaks preferentially at the MAR/SAR sites. The AF9 gene at 9p22 was targeted in this study because 9p22 is a deletion site commonly found in NPC.
机译:背景已知氧化应激涉及鼻咽癌(NPC)的大多数病因。处于氧化应激状态的细胞可能会发生凋亡。我们以前已经证明,氧化应激诱导的细胞凋亡可能是介导鼻咽上皮细胞染色体断裂的潜在机制。此外,胱天蛋白酶激活的脱氧核糖核酸酶(CAD)可能是介导氧化应激诱导的细胞凋亡过程中染色体断裂的重要因素。在细胞凋亡和染色体重排期间发生染色体断裂。染色体断裂倾向于聚集在某些区域,例如基质缔合区/支架附着区(MAR / SAR)。我们假设氧化应激诱导的细胞凋亡可能会导致MAR / SAR位点的染色体断裂。由于9p22是NPC中常见的缺失位点,因此本研究靶向9p22处的AF9基因。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号