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减少姐妹染色单体黏合可作为肿瘤外显率的修饰因子。

Reduced sister chromatid cohesion acts as a tumor penetrance modifier.

机构信息

Department of Pharmacology and Toxicology, University of Alabama at Birmingham Heersink School of Medicine, Birmingham, Alabama, United States of America.

Department of Genetics, University of Alabama at Birmingham Heersink School of Medicine, Birmingham, Alabama, United States of America.

出版信息

PLoS Genet. 2022 Aug 22;18(8):e1010341. doi: 10.1371/journal.pgen.1010341. eCollection 2022 Aug.

Abstract

Sister chromatid cohesion (SCC) is an important process in chromosome segregation. ESCO2 is essential for establishment of SCC and is often deleted/altered in human cancers. We demonstrate that esco2 haploinsufficiency results in reduced SCC and accelerates the timing of tumor onset in both zebrafish and mouse p53 heterozygous null models, but not in p53 homozygous mutant or wild-type animals. These data indicate that esco2 haploinsufficiency accelerates tumor onset in a loss of heterozygosity (LOH) sensitive background. Analysis of The Cancer Genome Atlas (TCGA) confirmed ESCO2 deficient tumors have elevated number of LOH events throughout the genome. Further, we demonstrated heterozygous loss of sgo1, important in maintaining SCC, also results in reduced SCC and accelerated tumor formation in a p53 heterozygous background. Surprisingly, while we did observe elevated levels of chromosome missegregation and micronuclei formation in esco2 heterozygous mutant animals, this chromosomal instability did not contribute to the accelerated tumor onset in a p53 heterozygous background. Interestingly, SCC also plays a role in homologous recombination, and we did observe elevated levels of mitotic recombination derived p53 LOH in tumors from esco2 haploinsufficient animals; as well as elevated levels of mitotic recombination throughout the genome of human ESCO2 deficient tumors. Together these data suggest that reduced SCC contributes to accelerated tumor penetrance through elevated mitotic recombination.

摘要

姐妹染色单体黏合(Sister chromatid cohesion,SCC)是染色体分离过程中的一个重要步骤。ESCO2 对于 SCC 的建立是必不可少的,并且经常在人类癌症中缺失/改变。我们证明,esco2 杂合不足导致 SCC 减少,并加速了斑马鱼和小鼠 p53 杂合缺失模型中肿瘤发生的时间,但在 p53 纯合突变或野生型动物中则不会。这些数据表明,esco2 杂合不足在杂合性丢失(Loss of heterozygosity,LOH)敏感背景下加速肿瘤的发生。对癌症基因组图谱(The Cancer Genome Atlas,TCGA)的分析证实,ESCO2 缺失的肿瘤在整个基因组中都有更多的 LOH 事件。此外,我们还证明了在维持 SCC 中重要的 sgo1 杂合缺失也会导致 SCC 减少,并在 p53 杂合背景下加速肿瘤的形成。令人惊讶的是,尽管我们在 esco2 杂合突变动物中观察到染色体错误分离和微核形成水平升高,但这种染色体不稳定性并没有导致 p53 杂合背景下肿瘤发生的加速。有趣的是,SCC 也在同源重组中发挥作用,我们确实观察到在 esco2 杂合不足动物的肿瘤中,有更高水平的有丝分裂重组衍生的 p53 LOH;以及在人类 ESCO2 缺失肿瘤的整个基因组中都有更高水平的有丝分裂重组。总之,这些数据表明,SCC 的减少通过增加有丝分裂重组导致肿瘤侵袭性增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22bb/9436123/e47058a77963/pgen.1010341.g001.jpg

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