Genome-wide CRISPR/Cas9 screening for drug resistance in tumors

被引:12
作者
Zhang, Zhongyan [1 ,2 ]
Wang, Hailiang [1 ,2 ,3 ]
Yan, Qian [1 ,4 ]
Cui, Jinwei [1 ,4 ]
Chen, Yubin [1 ,4 ]
Ruan, Shiye [1 ,2 ]
Yang, Jiayu [1 ,2 ]
Wu, Zelong [1 ,2 ]
Han, Mingqian [1 ,2 ]
Huang, Shanzhou [1 ]
Zhou, Qi [5 ,6 ]
Zhang, Chuanzhao [1 ]
Hou, Baohua [1 ,2 ]
机构
[1] Southern Med Univ, Guangdong Prov Peoples Hosp, Guangdong Acad Med Sci, Dept Gen Surg, Guangzhou, Peoples R China
[2] Southern Med Univ, Sch Clin Med 2, Guangzhou, Peoples R China
[3] Qingdao Univ, Weihai Cent Hosp, Dept Hepatobiliary Surg, Weihai, Peoples R China
[4] South China Univ Technol, Sch Med, Guangzhou, Peoples R China
[5] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Liver Surg, Guangzhou, Peoples R China
[6] Sun Yat Sen Univ, Hui Ya Hosp, Affiliated Hosp 1, Dept Gen Surg, Huizhou, Guangdong, Peoples R China
关键词
drug resistance; tumors; genome-wide CRISPR/Cas9 screening; MAPK pathway inhibitors; PARP inhibitors; TRANSCRIPTIONAL ACTIVATION; SORAFENIB RESISTANCE; CRISPR-CAS9; MECHANISMS; SENSITIVITY; EXPRESSION; VULNERABILITIES;
D O I
10.3389/fphar.2023.1284610
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Genome-wide clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR associated nuclease 9 (Cas9) screening is a simple screening method for locating loci under specific conditions, and it has been utilized in tumor drug resistance research for finding potential drug resistance-associated genes. This screening strategy has significant implications for further treatment of malignancies with acquired drug resistance. In recent years, studies involving genome-wide CRISPR/Cas9 screening have gradually increased. Here we review the recent application of genome-wide CRISPR/Cas9 screening for drug resistance, involving mitogen-activated protein kinase (MAPK) pathway inhibitors, poly (ADP-ribose) polymerase inhibitors (PARPi), alkylating agents, mitotic inhibitors, antimetabolites, immune checkpoint inhibitors (ICIs), and cyclin-dependent kinase inhibitors (CDKI). We summarize drug resistance pathways such as the KEAP1/Nrf2 pathway MAPK pathway, and NF-kappa B pathway. Also, we analyze the limitations and conditions for the application of genome-wide CRISPR/Cas9 screening techniques.
引用
收藏
页数:15
相关论文
共 102 条
[1]   Paclitaxel's Mechanistic and Clinical Effects on Breast Cancer [J].
Abu Samaan, Tala M. ;
Samec, Marek ;
Liskova, Alena ;
Kubatka, Peter ;
Busselberg, Dietrich .
BIOMOLECULES, 2019, 9 (12)
[2]   Genome-wide CRISPR screen reveals PSMA6 to be an essential gene in pancreatic cancer cells [J].
Bakke, Jesse ;
Wright, William C. ;
Zamora, Anthony E. ;
Oladimeji, Peter ;
Crawford, Jeremy Chase ;
Brewer, Christopher T. ;
Autry, Robert J. ;
Evans, William E. ;
Thomas, Paul G. ;
Chen, Taosheng .
BMC CANCER, 2019, 19 (1)
[3]   The CST Complex Mediates End Protection at Double-Strand Breaks and Promotes PARP Inhibitor Sensitivity in BRCA1-Deficient Cells [J].
Barazas, Marco ;
Annunziato, Stefano ;
Pettitt, Stephen J. ;
de Krijger, Inge ;
Ghezraoui, Hind ;
Roobol, Stefan J. ;
Lutz, Catrin ;
Frankum, Jessica ;
Song, Fei Fei ;
Brough, Rachel ;
Evers, Bastiaan ;
Gogola, Ewa ;
Bhin, Jinhyuk ;
van de Ven, Marieke ;
van Gent, Dik C. ;
Jacobs, Jacqueline J. L. ;
Chapman, Ross ;
Lord, Christopher J. ;
Jonkers, Jos ;
Rottenberg, Sven .
CELL REPORTS, 2018, 23 (07) :2107-2118
[4]   miR-6077 promotes cisplatin/pemetrexed resistance in lung adenocarcinoma via CDKN1A/cell cycle arrest and KEAP1/ferroptosis pathways [J].
Bi, Guoshu ;
Liang, Jiaqi ;
Zhao, Mengnan ;
Zhang, Huan ;
Jin, Xing ;
Lu, Tao ;
Zheng, Yuansheng ;
Bian, Yunyi ;
Chen, Zhencong ;
Huang, Yiwei ;
Besskaya, Valeria ;
Zhan, Cheng ;
Wang, Qun ;
Tan, Lijie .
MOLECULAR THERAPY NUCLEIC ACIDS, 2022, 28 :366-386
[5]   CMTM6 maintains the expression of PD-L1 and regulates anti-tumour immunity [J].
Burr, Marian L. ;
Sparbier, Christina E. ;
Chan, Yih-Chih ;
Williamson, James C. ;
Woods, Katherine ;
Beavis, Paul A. ;
Lam, Enid Y. N. ;
Henderson, Melissa A. ;
Bell, Charles C. ;
Stolzenburg, Sabine ;
Gilan, Omer ;
Bloor, Stuart ;
Noori, Tahereh ;
Morgens, David W. ;
Bassik, Michael C. ;
Neeson, Paul J. ;
Behren, Andreas ;
Darcy, Phillip K. ;
Dawson, Sarah-Jane ;
Voskoboinik, Ilia ;
Trapani, Joseph A. ;
Cebon, Jonathan ;
Lehner, Paul J. ;
Dawson, Mark A. .
NATURE, 2017, 549 (7670) :101-105
[6]   Genome-scale CRISPR activation screening identifies a role of LRP8 in Sorafenib resistance in Hepatocellular carcinoma [J].
Cai, Jun ;
Chen, Jianfei ;
Wu, Tiantian ;
Cheng, Zhilei ;
Tian, Yuanhu ;
Pu, Changsheng ;
Shi, Wenzai ;
Suo, Xiaopeng ;
Wu, Xianjia ;
Zhang, Keming .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2020, 526 (04) :1170-1176
[7]   Activation and Function of the MAPKs and Their Substrates, the MAPK-Activated Protein Kinases [J].
Cargnello, Marie ;
Roux, Philippe P. .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2011, 75 (01) :50-83
[8]   CRISPR-Cas9-based genome-wide screening identified novel targets for treating sorafenib-resistant hepatocellular carcinoma: a cross-talk between FGF21 and the NRF2 pathway [J].
Chen, Jiang ;
Jiang, Shi ;
Shao, Huijiang ;
Li, Bixia ;
Ji, Tong ;
Staiculescu, Daniel ;
He, Jiayan ;
Zhao, Jie ;
Cai, Liuxin ;
Liang, Xiao ;
Xu, Junjie ;
Cai, Xiujun .
SCIENCE CHINA-LIFE SCIENCES, 2022, 65 (10) :1998-2016
[9]   Smoothened-activating lipids drive resistance to CDK4/6 inhibition in Hedgehog-associated medulloblastoma cells and preclinical models [J].
Daggubati, Vikas ;
Hochstelter, Jordan ;
Bommireddy, Anirudh ;
Choudhury, Abrar ;
Krup, Alexis Leigh ;
Kaur, Pervinder ;
Tong, Pakteema ;
Li, Amy ;
Xu, Libin ;
Reiter, Jeremy F. ;
Raleigh, David R. .
JOURNAL OF CLINICAL INVESTIGATION, 2021, 131 (06)
[10]  
Datlinger P, 2017, NAT METHODS, V14, P297, DOI [10.1038/NMETH.4177, 10.1038/nmeth.4177]