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The Role of Aneuploidy in Cancer Evolution.非整倍体在癌症演进中的作用。
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2
Chromosomal instability accelerates the evolution of resistance to anti-cancer therapies.染色体不稳定性加速了对癌症疗法的耐药性的进化。
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Examining the link between chromosomal instability and aneuploidy in human cells.研究人类细胞中染色体不稳定性与非整倍体之间的联系。
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Cancer: a CINful evolution.癌症:一种有丝分裂失控的演变。
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本文引用的文献

1
Metastasis as an evolutionary process.转移作为一个进化过程。
Science. 2016 Apr 8;352(6282):169-75. doi: 10.1126/science.aaf2784.
2
Deletions linked to TP53 loss drive cancer through p53-independent mechanisms.与TP53缺失相关的缺失通过不依赖p53的机制驱动癌症。
Nature. 2016 Mar 24;531(7595):471-475. doi: 10.1038/nature17157. Epub 2016 Mar 16.
3
The Spindle Assembly Checkpoint Is Not Essential for Viability of Human Cells with Genetically Lowered APC/C Activity.纺锤体组装检验点对于APC/C活性基因下调的人类细胞的生存力并非必不可少。
Cell Rep. 2016 Mar 1;14(8):1829-40. doi: 10.1016/j.celrep.2016.01.060. Epub 2016 Feb 18.
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The presence of extra chromosomes leads to genomic instability.额外染色体的存在会导致基因组不稳定。
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Intact Cohesion, Anaphase, and Chromosome Segregation in Human Cells Harboring Tumor-Derived Mutations in STAG2.STAG2基因发生肿瘤源性突变的人类细胞中的完整黏连、后期及染色体分离
PLoS Genet. 2016 Feb 12;12(2):e1005865. doi: 10.1371/journal.pgen.1005865. eCollection 2016 Feb.
6
Effects of Anticancer Drugs on Chromosome Instability and New Clinical Implications for Tumor-Suppressing Therapies.抗癌药物对染色体不稳定性的影响及肿瘤抑制疗法的新临床意义。
Cancer Res. 2016 Feb 15;76(4):902-11. doi: 10.1158/0008-5472.CAN-15-1617. Epub 2016 Feb 2.
7
CHK2-BRCA1 tumor-suppressor axis restrains oncogenic Aurora-A kinase to ensure proper mitotic microtubule assembly.CHK2-BRCA1肿瘤抑制轴抑制致癌性极光激酶A以确保有丝分裂微管的正常组装。
Proc Natl Acad Sci U S A. 2016 Feb 16;113(7):1817-22. doi: 10.1073/pnas.1525129113. Epub 2016 Feb 1.
8
Divergent clonal selection dominates medulloblastoma at recurrence.不同的克隆选择在髓母细胞瘤复发时占主导地位。
Nature. 2016 Jan 21;529(7586):351-7. doi: 10.1038/nature16478. Epub 2016 Jan 13.
9
Chromothripsis and Kataegis Induced by Telomere Crisis.端粒危机引发的染色体碎裂和kataegis现象
Cell. 2015 Dec 17;163(7):1641-54. doi: 10.1016/j.cell.2015.11.054.
10
Replication stress activates DNA repair synthesis in mitosis.复制压力会在有丝分裂中激活 DNA 修复合成。
Nature. 2015 Dec 10;528(7581):286-90. doi: 10.1038/nature16139. Epub 2015 Dec 2.

非整倍体在癌症演进中的作用。

The Role of Aneuploidy in Cancer Evolution.

机构信息

Translational Cancer Therapeutics Laboratory, The Francis Crick Institute, Lincoln's Inn Fields Laboratories, London WC2A 3LY, United Kingdom.

CRUK Lung Cancer Centre of Excellence/UCL Cancer Institute, London WC1E 6BT, United Kingdom.

出版信息

Cold Spring Harb Perspect Med. 2017 Jan 3;7(1):a028373. doi: 10.1101/cshperspect.a028373.

DOI:10.1101/cshperspect.a028373
PMID:28049655
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5204330/
Abstract

Chromosomal aberrations during cell division represent one of the first recognized features of human cancer cells, and modern detection methods have revealed the pervasiveness of aneuploidy in cancer. The ongoing karyotypic changes brought about by chromosomal instability (CIN) contribute to tumor heterogeneity, drug resistance, and treatment failure. Whole-chromosome and segmental aneuploidies resulting from CIN have been proposed to allow "macroevolutionary" leaps that may contribute to profound phenotypic change. In this review, we will outline evidence indicating that aneuploidy and CIN contribute to cancer evolution.

摘要

染色体畸变在细胞分裂过程中代表了人类癌细胞的最早特征之一,现代检测方法已经揭示了非整倍体在癌症中的普遍性。染色体不稳定性 (CIN) 引起的持续的核型变化导致肿瘤异质性、耐药性和治疗失败。CIN 导致的全染色体和片段性非整倍体被认为可以允许“宏观进化”的飞跃,从而可能导致显著的表型变化。在这篇综述中,我们将概述表明非整倍体和 CIN 有助于癌症进化的证据。