Homologous Recombination Deficiency Unrelated to Platinum and PARP Inhibitor Response in Cell Line Libraries

被引:5
|
作者
Takamatsu, Shiro [1 ,2 ]
Murakami, Kosuke [3 ,4 ]
Matsumura, Noriomi [3 ]
机构
[1] Kyoto Univ, Grad Sch Med, Dept Gynecol & Obstet, Kyoto, Kyoto, Japan
[2] Univ Texas MD Anderson Canc Ctr, Dept Genom Med, Houston, TX USA
[3] Kindai Univ, Fac Med, Dept Obstet & Gynecol, Osakasayama, Osaka, Japan
[4] Johns Hopkins Univ, Bloomberg Kimmel Inst Canc Immunotherapy, Baltimore, MD USA
基金
日本学术振兴会;
关键词
DRUG-SENSITIVITY; DNA-REPAIR; CANCER; IDENTIFICATION; INSTABILITY; MECHANISM; RESOURCE;
D O I
10.1038/s41597-024-03018-4
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
While large publicly available cancer cell line databases are invaluable for preclinical drug discovery and biomarker development, the association between homologous recombination deficiency (HRD) and drug sensitivity in these resources remains unclear. In this study, we comprehensively analyzed molecular profiles and drug screening data from the Cancer Cell Line Encyclopedia. Unexpectedly, gene alterations in BRCA1/2 or homologous recombination-related genes, HRD scores, or mutational signature 3 were not positively correlated with sensitivity to platinum agents or PARP inhibitors. Rather, higher HRD scores and mutational signature 3 were significantly associated with resistance to these agents in multiple assays. These findings were consistent when analyzing exclusively breast and ovarian cancer cell lines and when using data from the COSMIC Cell Line Project. Collectively, the existing data from established cancer cell lines do not reflect the expected association between HRD status and drug response to platinum agents and PARP inhibitors in clinical tumors. This discrepancy may extend to other tumor characteristics, highlighting the importance of recognizing potential limitations in cell line data for researchers.
引用
收藏
页数:8
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