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

被引:4
|
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.
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页数:15
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