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模拟特定的非整倍体:从染色体组操作到生物学见解。

Modeling specific aneuploidies: from karyotype manipulations to biological insights.

机构信息

Oncode Institute and Center for Molecular Medicine, University Medical Center Utrecht, Universiteitsweg 100, 3584, CG, Utrecht, The Netherlands.

出版信息

Chromosome Res. 2023 Aug 29;31(3):25. doi: 10.1007/s10577-023-09735-7.

DOI:10.1007/s10577-023-09735-7
PMID:37640903
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10462580/
Abstract

An abnormal chromosome number, or aneuploidy, underlies developmental disorders and is a common feature of cancer, with different cancer types exhibiting distinct patterns of chromosomal gains and losses. To understand how specific aneuploidies emerge in certain tissues and how they contribute to disease development, various methods have been developed to alter the karyotype of mammalian cells and mice. In this review, we provide an overview of both classic and novel strategies for inducing or selecting specific chromosomal gains and losses in human and murine cell systems. We highlight how these customized aneuploidy models helped expanding our knowledge of the consequences of specific aneuploidies to (cancer) cell physiology.

摘要

异常染色体数量,即非整倍体,是发育障碍的基础,也是癌症的一个常见特征,不同类型的癌症表现出不同的染色体增益和丢失模式。为了了解特定组织中特定的非整倍体如何出现以及它们如何导致疾病的发展,已经开发出各种方法来改变哺乳动物细胞和小鼠的核型。在这篇综述中,我们提供了对诱导或选择人类和鼠类细胞系统中特定染色体增益和丢失的经典和新策略的概述。我们强调了这些定制的非整倍体模型如何帮助我们扩展对特定非整倍体对(癌症)细胞生理学的影响的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cb2/10462580/ea4d9a6d28fc/10577_2023_9735_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cb2/10462580/0ce8b349dcf0/10577_2023_9735_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cb2/10462580/6c2c522cf8e1/10577_2023_9735_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cb2/10462580/3713220b46aa/10577_2023_9735_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cb2/10462580/ea4d9a6d28fc/10577_2023_9735_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cb2/10462580/0ce8b349dcf0/10577_2023_9735_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cb2/10462580/6c2c522cf8e1/10577_2023_9735_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cb2/10462580/3713220b46aa/10577_2023_9735_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cb2/10462580/ea4d9a6d28fc/10577_2023_9735_Fig4_HTML.jpg

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Deletion of 17p in cancers: Guilt by (p53) association.癌症中17号染色体短臂缺失:因(p53)关联而获罪。
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Aneuploidy as a driver of human cancer.非整倍体作为人类癌症的驱动因素。

本文引用的文献

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Oncogene-like addiction to aneuploidy in human cancers.人类癌症中类似癌基因的非整倍体成瘾。
Science. 2023 Aug 25;381(6660):eadg4521. doi: 10.1126/science.adg4521.
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Loss of chromosome Y in primary tumors.原发性肿瘤中Y染色体缺失。
Cell. 2023 Jun 22. doi: 10.1016/j.cell.2023.06.006.
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Cancer aneuploidies are shaped primarily by effects on tumour fitness.癌症非整倍体主要由对肿瘤适应性的影响所决定。
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Patterns of Aneuploidy and Signaling Consequences in Cancer.癌症中的非整倍体模式和信号后果。
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Chromosome Transplantation: Opportunities and Limitations.染色体移植:机遇与限制。
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The two sides of chromosomal instability: drivers and brakes in cancer.染色体不稳定性的两面:癌症中的驱动因素和刹车。
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Two decades of chromosomal instability and aneuploidy.二十年的染色体不稳定和非整倍体状态。
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Y chromosome loss in cancer drives growth by evasion of adaptive immunity.Y 染色体缺失可通过逃避适应性免疫促进肿瘤生长。
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High-content CRISPR screening.高内涵CRISPR筛选
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KaryoCreate: A CRISPR-based technology to study chromosome-specific aneuploidy by targeting human centromeres.KaryoCreate:一种基于 CRISPR 的技术,通过靶向人类着丝粒研究染色体特异性非整倍性。
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Targeted assembly of ectopic kinetochores to induce chromosome-specific segmental aneuploidies.靶向组装异位着丝粒以诱导染色体特异性片段非整倍体。
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