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DNA损伤反应通路中的基因组、转录组和功能改变作为卵巢癌化疗反应的潜在生物标志物

Genomic, Transcriptomic, and Functional Alterations in DNA Damage Response Pathways as Putative Biomarkers of Chemotherapy Response in Ovarian Cancer.

作者信息

Sharma Saha Sweta, Gentles Lucy, Bradbury Alice, Brecht Dominik, Robinson Rebecca, O'Donnell Rachel, Curtin Nicola J, Drew Yvette

机构信息

Newcastle University Centre for Cancer, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.

Department of Chemsitry/Biology, University of Konstanz, 78464 Konstanz, Germany.

出版信息

Cancers (Basel). 2021 Mar 20;13(6):1420. doi: 10.3390/cancers13061420.

Abstract

Defective DNA damage response (DDR) pathways are enabling characteristics of cancers that not only can be exploited to specifically target cancer cells but also can predict chemotherapy response. Defective Homologous Recombination Repair (HRR) function, e.g., due to BRCA1/2 loss, is a determinant of response to platinum agents and PARP inhibitors in ovarian cancers. Most chemotherapies function by either inducing DNA damage or impacting on its repair but are generally used in the clinic unselectively. The significance of HRR and other DDR pathways in determining response to several other chemotherapy drugs is not well understood. In this study, the genomic, transcriptomic and functional analysis of DDR pathways in a panel of 14 ovarian cancer cell lines identified that defects in DDR pathways could determine response to several chemotherapy drugs. Carboplatin, rucaparib, and topotecan sensitivity were associated with functional loss of HRR (validated in 10 patient-derived primary cultures) and mismatch repair. Two DDR gene expression clusters correlating with treatment response were identified, with PARP10 identified as a novel marker of platinum response, which was confirmed in The Cancer Genome Atlas (TCGA) ovarian cancer cohort. Reduced non-homologous end-joining function correlated with increased sensitivity to doxorubicin, while cells with high intrinsic oxidative stress showed sensitivity to gemcitabine. In this era of personalised medicine, molecular/functional characterisation of DDR pathways could guide chemotherapy choices in the clinic allowing specific targeting of ovarian cancers.

摘要

有缺陷的DNA损伤反应(DDR)通路是癌症的特征,不仅可以被利用来特异性靶向癌细胞,还能预测化疗反应。例如,由于BRCA1/2缺失导致的同源重组修复(HRR)功能缺陷,是卵巢癌对铂类药物和PARP抑制剂反应的决定因素。大多数化疗药物通过诱导DNA损伤或影响其修复发挥作用,但在临床上通常是无差别使用。HRR和其他DDR通路在决定对其他几种化疗药物反应中的意义尚未完全明确。在本研究中,对14种卵巢癌细胞系的DDR通路进行基因组、转录组和功能分析发现,DDR通路缺陷可决定对几种化疗药物的反应。卡铂、鲁卡帕尼和拓扑替康敏感性与HRR(在10种患者来源的原代培养物中得到验证)和错配修复的功能丧失相关。鉴定出两个与治疗反应相关的DDR基因表达簇,PARP10被确定为铂反应的新标志物,这在癌症基因组图谱(TCGA)卵巢癌队列中得到了证实。非同源末端连接功能降低与对阿霉素敏感性增加相关,而具有高内源性氧化应激的细胞对吉西他滨敏感。在这个精准医学时代,DDR通路的分子/功能特征可指导临床化疗选择,实现对卵巢癌的特异性靶向治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1174/8003626/a64bf570f168/cancers-13-01420-g001.jpg

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