癌症和先天性综合征的非整倍体特征。

IF 7.7 2区 生物学 Q1 GENETICS & HEREDITY
Pan Cheng, Karan Singh, Roger H Reeves, Teresa Davoli
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引用次数: 0

摘要

非整倍体,以染色体的增加或减少为特征,在癌症和先天性非整倍体综合征中都起着关键作用。对于任何非整倍体,我们可以区分它的一般效应和它的染色体特异性效应。一般效应是指非整倍体诱导的常见细胞应激,如增殖受损、蛋白毒性应激和代谢改变,这些应激与特定的染色体无关,并深刻影响细胞和生物体的功能。这些普遍的压力通常会阻碍细胞的适应性,但在某些条件下,也会导致癌症的进展。相反,染色体特异性效应则是由于获得或失去的染色体上特定基因的剂量改变而产生的。这些影响取决于所涉及的染色体,可以在癌细胞或先天性非整倍体(如唐氏综合症)的不同发育表型中提供特定的适合性影响。了解这两种效应之间的相互作用对于破译非整倍体的结果至关重要。这篇综述综合了目前的知识,并讨论了未来的方向,揭示非整倍体的标志。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Hallmarks of Aneuploidy in Cancer and Congenital Syndromes.

Aneuploidy, characterized by the gain or loss of chromosomes, plays a critical role in both cancer and congenital aneuploidy syndromes. For any aneuploidy, we can distinguish between its general effects and its chromosome-specific effects. General effects refer to the common cellular stresses induced by aneuploidy, such as impaired proliferation, proteotoxic stress, and altered metabolism, which occur regardless of the specific chromosome involved and profoundly impact cellular and organismal functions. These generalized stresses often hinder cell fitness but can also, under certain conditions, contribute to cancer progression. In contrast, chromosome-specific effects arise from the altered dosage of particular genes on the gained or lost chromosome. These effects vary depending on the chromosome involved and can provide specific fitness effects in cancer cells or distinct developmental phenotypes in congenital aneuploidies like Down syndrome. Understanding the interplay between these two levels of effects is crucial for deciphering the outcomes of aneuploidy. This review synthesizes current knowledge and discusses future directions for unraveling the hallmarks of aneuploidy.

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来源期刊
CiteScore
14.90
自引率
1.10%
发文量
29
期刊介绍: Since its inception in 2000, the Annual Review of Genomics and Human Genetics has been dedicated to showcasing significant developments in genomics as they pertain to human genetics and the human genome. The journal emphasizes genomic technology, genome structure and function, genetic modification, human variation and population genetics, human evolution, and various aspects of human genetic diseases, including individualized medicine.
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