Decker Joseph T, Hobson Eric C, Zhang Yining, Shin Seungjin, Thomas Alexandra L, Jeruss Jacqueline S, Arnold Kelly B, Shea Lonnie D
Department of Biomedical Engineering, University of Michigan, 2200 Bonisteel, 1119 Gerstacker, Ann Arbor 48109, Michigan.
Department of Chemical Engineering, University of Michigan, Ann Arbor, Michigan.
Biotechnol Bioeng. 2017 Sep;114(9):2085-2095. doi: 10.1002/bit.26293. Epub 2017 May 18.
The development of resistance to targeted therapeutics is a challenging issue for the treatment of cancer. Cancers that have mutations in BRCA, a DNA repair protein, have been treated with poly(ADP-ribose) polymerase (PARP) inhibitors, which target a second DNA repair mechanism with the aim of inducing synthetic lethality. While these inhibitors have shown promise clinically, the development of resistance can limit their effectiveness as a therapy. This study investigated mechanisms of resistance in BRCA-mutated cancer cells (HCC1937) to Olaparib (AZD2281) using TRACER, a technique for measuring dynamics of transcription factor (TF) activity in living cells. TF activity was monitored in the parental HCC1937 cell line and two distinct resistant cell lines, one with restored wild-type BRCA1 and one with acquired resistance independent of BRCA1 for 48 h during treatment with Olaparib. Partial least squares discriminant analysis (PLSDA) was used to categorize the three cell types based on TF activity, and network analysis was used to investigate the mechanism of early response to Olaparib in the study cells. NOTCH signaling was identified as a common pathway linked to resistance in both Olaparib-resistant cell types. Western blotting confirmed upregulation of NOTCH protein, and sensitivity to Olaparib was restored through co-treatment with a gamma secretase inhibitor. The identification of NOTCH signaling as a common pathway contributing to PARP inhibitor resistance by TRACER indicates the efficacy of transcription factor dynamics in identifying targets for intervention in treatment-resistant cancer and provides a new method for determining effective strategies for directed chemotherapy. Biotechnol. Bioeng. 2017;114: 2085-2095. © 2017 Wiley Periodicals, Inc.
对靶向治疗产生耐药性是癌症治疗中的一个具有挑战性的问题。携带DNA修复蛋白BRCA突变的癌症,已使用聚(ADP - 核糖)聚合酶(PARP)抑制剂进行治疗,该抑制剂靶向另一种DNA修复机制,旨在诱导合成致死。虽然这些抑制剂在临床上已显示出前景,但耐药性的产生会限制其作为一种治疗方法的有效性。本研究使用TRACER(一种测量活细胞中转录因子(TF)活性动态的技术),研究了BRCA突变癌细胞(HCC1937)对奥拉帕尼(AZD2281)的耐药机制。在用奥拉帕尼治疗期间,对亲本HCC1937细胞系和两种不同的耐药细胞系(一种恢复了野生型BRCA1,另一种获得了与BRCA1无关的耐药性)的TF活性进行了48小时的监测。使用偏最小二乘判别分析(PLSDA)根据TF活性对三种细胞类型进行分类,并使用网络分析来研究研究细胞中对奥拉帕尼早期反应的机制。NOTCH信号通路被确定为两种奥拉帕尼耐药细胞类型中与耐药相关的共同途径。蛋白质印迹证实了NOTCH蛋白的上调,并且通过与γ-分泌酶抑制剂联合治疗恢复了对奥拉帕尼的敏感性。通过TRACER将NOTCH信号通路鉴定为导致PARP抑制剂耐药的共同途径,表明转录因子动态在识别治疗耐药癌症的干预靶点方面的有效性,并为确定定向化疗的有效策略提供了一种新方法。生物技术与生物工程。2017年;114:2085 - 2095。©2017威利期刊公司