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DNA错配修复和临床肿瘤新进展

马守成 赵达

基础医学与临床2011,Vol.31Issue(12):1402-1405,4.
基础医学与临床2011,Vol.31Issue(12):1402-1405,4.

DNA错配修复和临床肿瘤新进展

The news for MMR and clinical cancer

马守成 1赵达1

作者信息

  • 1. 兰州大学第一医院肿瘤内,甘肃兰州730000
  • 折叠

摘要

Abstract

DNA replication is an extraordinarily faithful process, mutation occures at a frequency of 1/10 or 1/10 base pairs per cell division. The MMR pathway, a DNA repair pathway conserved from bacteria to humans, targets base substitution mismatches and insertion-deletion mismatches that arise as a result of replication errors that escape the proofreading function of DNA polymerases. In doing so, MMR contributes an additional 50 ~ 1000-fold to the o-verall fidelity of replication. Thus, inactivation of MMR confers a strong mutated phenotype in which the rate of spontaneous mutation is greatly elevated,such as microsatellite stability (MSI) , or mutated genes that code functional proteins, thus give rise to cancer.

关键词

DNA错配修复/微卫星不稳定性/结直肠肿瘤/乳腺肿瘤/前列腺肿瘤/神经胶质瘤

Key words

DNA MMR/ MSI/ HNPCC (CRC)/ breast cancer/ piwstate cancer Glioma

分类

生物科学

引用本文复制引用

马守成,赵达..DNA错配修复和临床肿瘤新进展[J].基础医学与临床,2011,31(12):1402-1405,4.

基础医学与临床

OA北大核心CSCDCSTPCD

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