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DNA 解旋酶基因的表达与乳腺癌同源重组缺陷相关。

Expression of DNA Helicase Genes Was Correlated with Homologous Recombination Deficiency in Breast Cancer.

机构信息

Department of Pathology, Peking University Cancer Hospital, Beijing, China.

Department of Breast Surgery, Peking University People's Hospital, Beijing, China.

出版信息

Comput Math Methods Med. 2022 Jul 9;2022:5508301. doi: 10.1155/2022/5508301. eCollection 2022.

DOI:10.1155/2022/5508301
PMID:35855837
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9288330/
Abstract

Homologous recombination deficiency which is currently measured by the homologous recombination deficiency (HRD) score including score of telomeric allelic imbalance (TAI), large-scale transition (LST), and loss of heterozygosity (LOH) is highly related with sensitivity to platinum-containing drug and PARP inhibitors. DNA helicases are essential components for the homologous recombination repair process in which DNA helicases unwind double-strand DNA utilizing ATP hydrolysis. In our study, the correlation between the expression of DNA helicase genes and HRD score in breast cancer was analyzed. The overexpression in half of the DNA helicase genes was found to be highly correlated with a high HRD score both in BRCA-mutated and BRCA wild-type breast cancer. Moreover, HRD score can be predicted by a linear function contributed by five DNA helicase genes. In conclusion, our study revealed a close relation between the overexpression of certain DNA helicase genes and the deficiency of homologous recombination repair in breast cancer.

摘要

同源重组缺陷(HRD)评分目前可通过包括端粒等位基因不平衡(TAI)、大片段转移(LST)和杂合性丢失(LOH)评分来衡量,与铂类药物和 PARP 抑制剂的敏感性高度相关。DNA 解旋酶是同源重组修复过程中的必需组成部分,该过程中 DNA 解旋酶利用 ATP 水解解开双链 DNA。在本研究中,分析了 DNA 解旋酶基因的表达与乳腺癌 HRD 评分之间的相关性。结果发现,在 BRCA 突变型和 BRCA 野生型乳腺癌中,有一半的 DNA 解旋酶基因的过表达与高 HRD 评分高度相关。此外,HRD 评分可以通过由 5 个 DNA 解旋酶基因组成的线性函数来预测。综上所述,本研究揭示了某些 DNA 解旋酶基因的过表达与乳腺癌同源重组修复缺陷之间的密切关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deee/9288330/5613853bb250/CMMM2022-5508301.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deee/9288330/a05e079e5e37/CMMM2022-5508301.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deee/9288330/8453b7214211/CMMM2022-5508301.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deee/9288330/ddaf38a310c5/CMMM2022-5508301.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deee/9288330/ce89e02f45ef/CMMM2022-5508301.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deee/9288330/5613853bb250/CMMM2022-5508301.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deee/9288330/a05e079e5e37/CMMM2022-5508301.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deee/9288330/8453b7214211/CMMM2022-5508301.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deee/9288330/ddaf38a310c5/CMMM2022-5508301.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deee/9288330/ce89e02f45ef/CMMM2022-5508301.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deee/9288330/5613853bb250/CMMM2022-5508301.005.jpg

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Classification of PR-positive and PR-negative subtypes in ER-positive and HER2-negative breast cancers based on pathway scores.基于通路评分对 ER 阳性和 HER2 阴性乳腺癌中 PR 阳性和 PR 阴性亚型进行分类。
BMC Med Res Methodol. 2021 May 22;21(1):108. doi: 10.1186/s12874-021-01297-8.
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A Histone Acetylation Modulator Gene Signature for Classification and Prognosis of Breast Cancer.
一种用于乳腺癌分类和预后的组蛋白乙酰化调节剂基因特征。
Curr Oncol. 2021 Feb 17;28(1):928-939. doi: 10.3390/curroncol28010091.
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Pharmacological targeting of differential DNA repair, radio-sensitizes WRN-deficient cancer cells in vitro and in vivo.靶向差异 DNA 修复的药理学方法可在体外和体内使 WRN 缺陷型癌细胞对放射增敏。
Biochem Pharmacol. 2021 Apr;186:114450. doi: 10.1016/j.bcp.2021.114450. Epub 2021 Feb 8.
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Targeting RECQL5 Functions, by a Small Molecule, Selectively Kills Breast Cancer o and .小分子靶向 RECQL5 功能,选择性杀伤乳腺癌 o 和 。
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Targeting autophagy reverses de novo resistance in homologous recombination repair proficient breast cancers to PARP inhibition.靶向自噬可逆转同源重组修复功能正常的乳腺癌对 PARP 抑制的新生耐药性。
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