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全臂染色体总缺失可预测人类癌症的恶性程度。

Total whole-arm chromosome losses predict malignancy in human cancer.

作者信息

Zheng Ye, Ahmad Kami, Henikoff Steven

机构信息

Basic Sciences Division, Fred Hutchinson Cancer Center, Seattle, WA 98109.

HHMI, Chevy Chase, MD 20815.

出版信息

Proc Natl Acad Sci U S A. 2025 May 6;122(18):e2505385122. doi: 10.1073/pnas.2505385122. Epub 2025 May 2.

DOI:10.1073/pnas.2505385122
PMID:40314975
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12067283/
Abstract

Aneuploidy is observed as gains or losses of whole chromosomes or chromosome arms and is a common hallmark of cancer. Whereas models for the generation of aneuploidy in cancer invoke mitotic chromosome segregation errors, whole-arm losses might occur simply as a result of centromere breakage. We recently showed that elevated RNA Polymerase II level over the S-phase-dependent histone genes predicts rapid recurrence of human meningioma and is correlated with total whole-arm losses relative to gains. To explain this imbalance in arm losses over gains, we have proposed that histone overexpression at S-phase competes with the histone H3 variant CENP-A, resulting in centromere breaks and whole-arm losses. To test whether centromere breaks alone can drive aneuploidy, we ask whether total whole-arm aneuploids can predict outcomes across different cancer types in large RNA and whole-genome sequencing databanks. We find that total whole-arm losses generally predict outcome, suggesting that centromere breakage is a major initiating factor leading to aneuploidy and the resulting changes in the selective landscape that drive most cancers. We also present evidence that centromere breakage alone is sufficient to account for whole-arm losses and gains, contrary to mitotic spindle error models for the generation of aneuploidy. Our results suggest that therapeutic intervention targeting histone overexpression has the potential to reduce aneuploidy and slow cancer progression.

摘要

非整倍体表现为整条染色体或染色体臂的增加或减少,是癌症的一个常见特征。虽然癌症中非整倍体产生的模型涉及有丝分裂染色体分离错误,但整条染色体臂的丢失可能仅仅是着丝粒断裂的结果。我们最近发现,在依赖S期的组蛋白基因上RNA聚合酶II水平升高预示着人类脑膜瘤的快速复发,并且与整条染色体臂丢失相对于增加的总数相关。为了解释染色体臂丢失相对于增加的这种不平衡,我们提出S期组蛋白过表达与组蛋白H3变体CENP - A竞争,导致着丝粒断裂和整条染色体臂丢失。为了测试仅着丝粒断裂是否能驱动非整倍体,我们在大型RNA和全基因组测序数据库中询问整条染色体臂非整倍体是否能预测不同癌症类型的预后。我们发现整条染色体臂的总体丢失通常能预测预后,这表明着丝粒断裂是导致非整倍体以及驱动大多数癌症的选择性景观变化的一个主要起始因素。我们还提供证据表明,与非整倍体产生的有丝分裂纺锤体错误模型相反,仅着丝粒断裂就足以解释整条染色体臂的丢失和增加。我们的结果表明,针对组蛋白过表达的治疗干预有可能减少非整倍体并减缓癌症进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d19/12067283/744060159286/pnas.2505385122fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d19/12067283/562adbf009df/pnas.2505385122fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d19/12067283/1408c4802a03/pnas.2505385122fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d19/12067283/1856ec67e8ad/pnas.2505385122fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d19/12067283/744060159286/pnas.2505385122fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d19/12067283/562adbf009df/pnas.2505385122fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d19/12067283/1408c4802a03/pnas.2505385122fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d19/12067283/1856ec67e8ad/pnas.2505385122fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d19/12067283/744060159286/pnas.2505385122fig04.jpg

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PBRM1 directs PBAF to pericentromeres and protects centromere integrity.PBRM1将PBAF引导至着丝粒周围并保护着丝粒的完整性。
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Centromeres are stress-induced fragile sites.着丝粒是应激诱导的脆弱位点。
Curr Biol. 2025 Mar 24;35(6):1197-1210.e4. doi: 10.1016/j.cub.2025.01.055. Epub 2025 Feb 18.
4
RNA polymerase II at histone genes predicts outcome in human cancer.组蛋白基因处的RNA聚合酶II可预测人类癌症的预后。
Science. 2025 Jan 2;387(6735):737-743. doi: 10.1126/science.ads2169. Epub 2025 Feb 13.
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Meningioma transcriptomic landscape demonstrates novel subtypes with regional associated biology and patient outcome.脑膜瘤转录组图谱揭示了具有区域相关生物学特性和患者预后的新型亚型。
Cell Genom. 2024 Jun 12;4(6):100566. doi: 10.1016/j.xgen.2024.100566. Epub 2024 May 23.
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7
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