Assessment of genetic damage in healthy and diseased tissue.

IARC scientific publications Pub Date : 2011-01-01
Joe Shuga, Pierre Hainaut, Martyn T Smith
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Abstract

DNA, along with other cellular components, is under constant attack by chemical, physical, and infectious agents present in the human environment, as well as by reactive metabolites generated by physiological processes. Mutations occur as the consequence of this damage, but may also be caused by improper DNA repair of alterations occurring during normal DNA replication and transcription. Genetic damage can occur at the level of the gene (e.g. point mutations, insertions, and deletions) or at the level of the chromosome (e.g. aneuploidy, translocations). Further, mutations can also take place in mitochondrial DNA. Another form of DNA modification is epigenetic methylation of CpG islands, which affects the dynamics of chromatin as well as the expression of a large panel of genes. Recent technical advances have improved the capacity to detect and quantify genetic and epigenetic changes. This chapter summarizes current knowledge on mechanisms of DNA damage and mutagenesis, laying out the concepts for interpreting mutations as biomarkers in investigating the causes and consequences of cancer. It also outlines both established and novel methods for detecting genetic and epigenetic changes in normal and diseased tissues, and then discusses their application in the realm of molecular epidemiology.

评估健康和病变组织的遗传损伤。
DNA和其他细胞成分不断受到人类环境中存在的化学、物理和感染因子以及生理过程产生的反应性代谢物的攻击。突变是这种损伤的结果,但也可能是由正常DNA复制和转录过程中发生的DNA修复不当引起的。遗传损伤可发生在基因水平(如点突变、插入和缺失)或染色体水平(如非整倍体、易位)。此外,线粒体DNA也可能发生突变。另一种形式的DNA修饰是CpG岛的表观遗传甲基化,它影响染色质的动力学以及大量基因的表达。最近的技术进步提高了检测和量化遗传和表观遗传变化的能力。本章总结了目前关于DNA损伤和诱变机制的知识,提出了在研究癌症的原因和后果时将突变解释为生物标志物的概念。它还概述了在正常和病变组织中检测遗传和表观遗传变化的既有方法和新方法,然后讨论了它们在分子流行病学领域的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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