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Accumulation of genetic and epigenetic alterations in normal cells and cancer risk

机译:正常细胞中遗传和表观遗传改变的积累和癌症风险

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摘要

Cancers develop due to the accumulation of genetic and epigenetic alterations. Genetic alterations are induced by aging, mutagenic chemicals, ultraviolet light, and other factors; whereas, epigenetic alterations are mainly by aging and chronic inflammation. The accumulation and patterns of alterations in normal cells reflect our past exposure levels and life history. Most accumulated alterations are considered as passengers, but their accumulation is correlated with cancer drivers. This has been shown for aberrant DNA methylation but has only been speculated for genetic alterations. However, recent technological advancements have enabled measurement of rare point mutations, and studies have shown that their accumulation levels are indeed correlated with cancer risk. When the accumulation levels of aberrant DNA methylation and point mutations are combined, risk prediction becomes even more accurate. When high levels of alterations accumulate, the tissue has a high risk of developing cancer or even multiple cancers and is considered as a “cancerization field”, with or without expansion of physiological patches of clonal cells. In this review, we describe the formation of a cancerization field and how we can apply its detection in precision cancer risk diagnosis.
机译:癌症由于遗传和表观遗传学改变的积累而发展。遗传改变是由衰老,诱变化学物质,紫外线和其他因素引起的。然而,表观遗传改变主要是由于衰老和慢性炎症。正常细胞中积累和变化的模式反映了我们过去的暴露水平和生活史。大多数积累的变化被认为是乘客,但其积累与癌症驱动因素有关。对于异常的DNA甲基化已显示出这种现象,但仅推测其遗传改变。但是,最近的技术进步已经能够测量稀有点突变,并且研究表明它们的积累水平确实与癌症风险相关。当异常DNA甲基化的累积水平和点突变结合在一起时,风险预测将变得更加准确。当高水平的改变积累时,组织具有发展癌症或什至是多种癌症的高风险,并且被认为是“癌变场”,具有或不具有克隆细胞的生理斑块的扩展。在这篇综述中,我们描述了癌变场的形成以及如何将其检测应用于精确的癌症风险诊断。

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