Response prediction biomarkers and drug combinations of PARP inhibitors in prostate cancer

被引:7
作者
Chen, Yi-xin [1 ,2 ,3 ]
Tan, Li-ming [4 ]
Gong, Jian-ping [4 ]
Huang, Ma-sha [1 ,2 ,3 ]
Yin, Ji-ye [1 ,2 ,3 ]
Zhang, Wei [1 ,2 ,3 ]
Zhou, Hong-hao [1 ,2 ,3 ]
Liu, Zhao-qian [1 ,2 ,3 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Clin Pharmacol, Hunan Key Lab Pharmacogenet, Changsha 410008, Peoples R China
[2] Cent South Univ, Xiangya Hosp, Natl Clin Res Ctr Geriatr Disorders, Changsha 410008, Peoples R China
[3] Cent South Univ, Inst Clin Pharmacol, Engn Res Ctr Appl Technol Pharmacogen, Minist Educ, Changsha 410078, Peoples R China
[4] Second Peoples Hosp Huaihua City, Dept Pharm, Huaihua 418000, Peoples R China
基金
中国国家自然科学基金;
关键词
prostate cancer; PARP inhibitors; response prediction biomarkers; synergistic combination strategies; DNA-REPAIR DEFECTS; CELL-FREE DNA; POLY(ADP-RIBOSE) POLYMERASE; PATIENTS PTS; PHASE-II; HOMOLOGOUS RECOMBINATION; PEMBROLIZUMAB PEMBRO; DAMAGE RESPONSE; PLUS OLAPARIB; PTEN DELETION;
D O I
10.1038/s41401-020-00604-1
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
PARP inhibitors are a group of inhibitors targeting poly(ADP-ribose) polymerases (PARP1 or PARP2) involved in DNA repair and transcriptional regulation, which may induce synthetic lethality in BRCAness tumors. Systematic analyzes of genomic sequencing in prostate cancer show that similar to 10%-19% of patients with primary prostate cancer have inactivated DNA repair genes, with a notably higher proportion of 23%-27% in patients with metastatic castration-resistant prostate cancer (mCRPC). These characteristic genomic alterations confer possible vulnerability to PARP inhibitors in patients with mCRPC who benefit only modestly from other therapies. However, only a small proportion of patients with mCRPC shows sensitivity to PARP inhibitors, and these sensitive patients cannot be fully identified by existing response prediction biomarkers. In this review, we provide an overview of the potential response prediction biomarkers and synergistic combinations studied in the preclinical and clinical stages, which may expand the population of patients with prostate cancer who may benefit from PARP inhibitors.
引用
收藏
页码:1970 / 1980
页数:11
相关论文
共 123 条
[41]   Studies on prostate cancer II The effects of castration on advanced carcinoma of the prostate gland [J].
Huggins, C ;
Stevens, RE ;
Hodges, CV .
ARCHIVES OF SURGERY, 1941, 43 (02) :209-223
[42]   Targeting Androgen Receptor and DNA Repair in Metastatic Castration-Resistant Prostate Cancer: Results From NCI 9012 [J].
Hussain, Maha ;
Daignault-Newton, Stephanie ;
Twardowski, Przemyslaw W. ;
Albany, Costantine ;
Stein, Mark N. ;
Kunju, Lakshmi P. ;
Siddiqui, Javed ;
Wu, Yi-Mi ;
Robinson, Dan ;
Lonigro, Robert J. ;
Cao, Xuhong ;
Tomlins, Scott A. ;
Mehra, Rohit ;
Cooney, Kathleen A. ;
Montgomery, Bruce ;
Antonarakis, Emmanuel S. ;
Shevrin, Daniel H. ;
Corn, Paul G. ;
Whang, Young E. ;
Smith, David C. ;
Caram, Megan V. ;
Knudsen, Karen E. ;
Stadler, Walter M. ;
Feng, Felix Y. ;
Chinnaiyan, Arul M. .
JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (10) :991-+
[43]   Targeting DNA repair with combination veliparib (ABT-888) and temozolomide in patients with metastatic castration-resistant prostate cancer [J].
Hussain, Maha ;
Carducci, Michael A. ;
Slovin, Susan ;
Cetnar, Jeremy ;
Qian, Jiang ;
McKeegan, Evelyn M. ;
Refici-Buhr, Marion ;
Chyla, Brenda ;
Shepherd, Stacie P. ;
Giranda, Vincent L. ;
Alumkal, Joshi J. .
INVESTIGATIONAL NEW DRUGS, 2014, 32 (05) :904-912
[44]   Loss of INPP4B causes a DNA repair defect through loss of BRCA1, ATM and ATR and can be targeted with PARP inhibitor treatment [J].
Ip, Laura R. H. ;
Poulogiannis, George ;
Viciano, Felipe Cia ;
Sasaki, Junko ;
Kofuji, Satoshi ;
Spanswick, Victoria J. ;
Hochhauser, Daniel ;
Hartley, John A. ;
Sasaki, Takehiko ;
Gewinner, Christina A. .
ONCOTARGET, 2015, 6 (12) :10548-10562
[45]   ATM-Deficient Cancers Provide New Opportunities for Precision Oncology [J].
Jette, Nicholas R. ;
Kumar, Mehul ;
Radhamani, Suraj ;
Arthur, Greydon ;
Goutam, Siddhartha ;
Yip, Steven ;
Kolinsky, Michael ;
Williams, Gareth J. ;
Bose, Pinaki ;
Lees-Miller, Susan P. .
CANCERS, 2020, 12 (03)
[46]   Combined poly-ADP ribose polymerase and ataxia-telangiectasia mutated/Rad3-related inhibition targets ataxia-telangiectasia mutated-deficient lung cancer cells [J].
Jette, Nicholas R. ;
Radhamani, Suraj ;
Arthur, Greydon ;
Ye, Ruiqiong ;
Goutam, Siddhartha ;
Bolyos, Anthony ;
Petersen, Lars F. ;
Bose, Pinaki ;
Bebb, D. Gwyn ;
Lees-Miller, Susan P. .
BRITISH JOURNAL OF CANCER, 2019, 121 (07) :600-610
[47]  
Jette NR, 2020, Genome Instab. Dis., V1, P197
[48]   PARP Inhibitor Upregulates PD-L1 Expression and Enhances Cancer-Associated Immunosuppression [J].
Jiao, Shiping ;
Xia, Weiya ;
Yamaguchi, Hirohito ;
Wei, Yongkun ;
Chen, Mei-Kuang ;
Hsu, Jung-Mao ;
Hsu, Jennifer L. ;
Yu, Wen-Hsuan ;
Du, Yi ;
Lee, Heng-Huan ;
Li, Chia-Wei ;
Chou, Chao-Kai ;
Lim, Seung-Oe ;
Chang, Shih-Shin ;
Litton, Jennifer ;
Arun, Banu ;
Hortobagyi, Gabriel N. ;
Hung, Mien-Chie .
CLINICAL CANCER RESEARCH, 2017, 23 (14) :3711-3720
[49]   Stabilization of mutant BRCA1 protein confers PARP inhibitor and platinum resistance [J].
Johnson, Neil ;
Johnson, Shawn F. ;
Yao, Wei ;
Li, Yu-Chen ;
Choi, Young-Eun ;
Bernhardy, Andrea J. ;
Wang, Yifan ;
Capelletti, Marzia ;
Sarosiek, Kristopher A. ;
Moreau, Lisa A. ;
Chowdhury, Dipanjan ;
Wickramanayake, Anneka ;
Harrell, Maria I. ;
Liu, Joyce F. ;
D'Andrea, Alan D. ;
Miron, Alexander ;
Swisher, Elizabeth M. ;
Shapiro, Geoffrey I. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (42) :17041-17046
[50]   Cediranib suppresses homology-directed DNA repair through down-regulation of BRCA1/2 and RAD51 [J].
Kaplan, Alanna R. ;
Gueble, Susan E. ;
Liu, Yanfeng ;
Oeck, Sebastian ;
Kim, Hoon ;
Yun, Zhong ;
Glazer, Peter M. .
SCIENCE TRANSLATIONAL MEDICINE, 2019, 11 (492)