首页> 外文期刊>Pathobiology: journal of immunopathology, molecular and cellular biology >Expression of MRE11 complex (MRE11, RAD50, NBS1) and hRap1 and its relation with telomere regulation, telomerase activity in human gastric carcinomas.
【24h】

Expression of MRE11 complex (MRE11, RAD50, NBS1) and hRap1 and its relation with telomere regulation, telomerase activity in human gastric carcinomas.

机译:MRE11复合物(MRE11,RAD50,NBS1)和hRap1的表达及其与端粒调节,端粒酶活性在人胃癌中的关系。

获取原文
获取原文并翻译 | 示例
       

摘要

The MRE11 complex (MRE11, RAD50, NBS1) are required for the repair of DNA double-strand breaks and have another important function in regulating telomere length. The silent information regulator (Sir) proteins required for telomere position effect also bind telomeres. hRap1 protein is a human ortholog of yeast Rap1 which regulates telomere length by interacting with TRF2 and is recruited to telomeres by TRF2. We examined the expression of the MRE11 complex (MRE11, RAD50, NBS1), Sir2 and hRAP1 in 20 gastric carcinomas by reverse transcription polymerase chain reaction and then analyzed the relation between telomerase activity and other telomerase components such as human telomerase reverse transcriptase (TERT), human telomerase RNA component (hTR), human telomerase-associated protein (TEP1), telomeric repeat binding factor 1 (TRF1), TRF2- and TRF1-interacting, ankyrin-related ADP-ribose polymerase (tankyrase) as well as TRF1-interacting nuclear protein 2 (TIN2). Of twenty gastric carcinomas examined, 13 (65%), 14 (70%), 16 (80%), 12 (60%) and 13 (65%) expressed MRE11, RAD50, NBS1, Sir2 and hRap1 at higher levels than corresponding nonneoplastic gastric mucosa, respectively. No obvious correlation was observed between MRE11 complex expression and telomerase activity or expression of TERT, hTR, TEP1, tankyrase and TIN2. Carcinomas with high TRF1 expression expressed significantly higher levels of MRE11 and RAD50 than those with low TRF1 expression (p < 0.05). On the other hand, carcinomas with high TRF2 expression expressed significantly higher levels of MRE11, NBS1 and hRap1 than those with low TRF2 expression (p < 0.05). These results suggest that gastric carcinomas with high TRF1 and TRF2 expression may need a large quantity of the MRE11 complex. Moreover, gastric carcinomas with high TRF1 expression may require a large quantity of hRap1. Copyright 2002 S. Karger AG, Basel
机译:MRE11复合物(MRE11,RAD50,NBS1)是修复DNA双链断裂所必需的,并且在调节端粒长度方面具有另一重要功能。端粒位置效应所需的沉默信息调节剂(Sir)蛋白也结合端粒。 hRap1蛋白是酵母Rap1的人类直系同源基因,它通过与TRF2相互作用来调节端粒长度,并被TRF2募集到端粒中。我们通过逆转录聚合酶链反应检查了20种胃癌中MRE11复合物(MRE11,RAD50,NBS1),Sir2和hRAP1的表达,然后分析了端粒酶活性与其他端粒酶成分(例如人端粒酶逆转录酶(TERT))之间的关系。 ,人类端粒酶RNA成分(hTR),人类端粒酶相关蛋白(TEP1),端粒重复结合因子1(TRF1),TRF2-和TRF1相互作用,锚蛋白相关的ADP-核糖聚合酶(tankyrase)以及TRF1相互作用核蛋白2(TIN2)。在检查的二十种胃癌中,有13种(65%),14种(70%),16种(80%),12种(60%)和13种(65%)的MRE11,RAD50,NBS1,Sir2和hRap1的表达水平高于相应水平。非肿瘤性胃黏膜,分别。在MRE11复合物表达与端粒酶活性或TERT,hTR,TEP1,tankyrase和TIN2的表达之间未观察到明显的相关性。 TRF1高表达的癌组织的MRE11和RAD50水平显着高于TRF1低表达的癌组织(p <0.05)。另一方面,TRF2表达高的癌症的MRE11,NBS1和hRap1的表达水平明显高于TRF2表达低的癌症(p <0.05)。这些结果表明,具有高TRF1和TRF2表达的胃癌可能需要大量的MRE11复合物。此外,高TRF1表达的胃癌可能需要大量的hRap1。版权所有2002 S. Karger AG,巴塞尔

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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