Emerging strategies to overcome resistance to third-generation EGFR inhibitors

被引:110
作者
Shi, Kunyu [1 ,8 ]
Wang, Guan [1 ]
Pei, Junping [1 ]
Zhang, Jifa [1 ,8 ]
Wang, Jiaxing [2 ]
Ouyang, Liang [1 ,3 ,4 ,5 ,8 ]
Wang, Yuxi [1 ,6 ,7 ,8 ]
Li, Weimin [1 ,6 ,7 ,8 ]
机构
[1] Sichuan Univ, West China Hosp, Innovat Ctr Nursing Res,Dept Resp & Crit Care Med, Inst Resp Hlth,Nursing Key Lab Sichuan Prov,Targe, Chengdu 610041, Peoples R China
[2] Univ Tennessee, Coll Pharm, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USA
[3] Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Chengdu 610041, Peoples R China
[4] Sichuan Univ, West China Hosp, Canc Ctr, Chengdu 610041, Peoples R China
[5] Sichuan Univ, West China Hosp, Collaborat Innovat Ctr Biotherapy, Chengdu 610041, Peoples R China
[6] Sichuan Univ, West China Hosp, Precis Med Key Lab Sichuan Prov, Chengdu 610041, Peoples R China
[7] Sichuan Univ, West China Hosp, Precis Med Res Ctr, Chengdu 610041, Peoples R China
[8] Tianfu Jincheng Lab, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金;
关键词
Epidermal growth factor receptor (EGFR); Drug resistance; Inhibitors; Structure-activity relationship; Tyrosine kinase; Cancer; CELL LUNG-CANCER; TYROSINE KINASE INHIBITORS; DUAL EGFR/HER2 INHIBITORS; MUTANT NSCLC CELLS; ACQUIRED-RESISTANCE; PROTEIN-DEGRADATION; APOPTOSIS INDUCERS; 1ST-LINE TREATMENT; DRUG-RESISTANCE; TUMOR-CELLS;
D O I
10.1186/s13045-022-01311-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epidermal growth factor receptor (EGFR), the receptor for members of the epidermal growth factor family, regulates cell proliferation and signal transduction; moreover, EGFR is related to the inhibition of tumor cell proliferation, angiogenesis, invasion, metastasis, and apoptosis. Therefore, EGFR has become an important target for the treatment of cancer, including non-small cell lung cancer, head and neck cancer, breast cancer, glioma, cervical cancer, and bladder cancer. First- to third-generation EGFR inhibitors have shown considerable efficacy and have significantly improved disease prognosis. However, most patients develop drug resistance after treatment. The challenge of overcoming intrinsic and acquired resistance in primary and recurrent cancer mediated by EGFR mutations is thus driving the search for alternative strategies in the design of new therapeutic agents. In view of resistance to third-generation inhibitors, understanding the intricate mechanisms of resistance will offer insight for the development of more advanced targeted therapies. In this review, we discuss the molecular mechanisms of resistance to third-generation EGFR inhibitors and review recent strategies for overcoming resistance, new challenges, and future development directions.
引用
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页数:44
相关论文
共 217 条
[11]   L718Q mutant EGFR escapes covalent inhibition by stabilizing a non-reactive conformation of the lung cancer drug osimertinib [J].
Callegari, D. ;
Ranaghan, K. E. ;
Woods, C. J. ;
Minari, R. ;
Tiseo, M. ;
Mor, M. ;
Mulholland, A. J. ;
Lodola, A. .
CHEMICAL SCIENCE, 2018, 9 (10) :2740-2749
[12]   EPIDERMAL GROWTH FACTOR-LIKE MODULES [J].
CAMPBELL, ID ;
BORK, P .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 1993, 3 (03) :385-392
[13]   Degradation of MCL-1 by bufalin reverses acquired resistance to osimertinib in EGFR-mutant lung cancer [J].
Cao, Fei ;
Gong, Ya-Bin ;
Kang, Xiao-Hong ;
Lu, Zhi-Hong ;
Wang, Ying ;
Zhao, Ke-Lei ;
Miao, Zhan-Hui ;
Liao, Ming-Juan ;
Xu, Zhen-Ye .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2019, 379
[14]   The cellular geography of aurora kinases [J].
Carmena, M ;
Earnshaw, WC .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (11) :842-854
[15]   A Novel Acquired Exon 20 EGFR M766Q Mutation in Lung Adenocarcinoma Mediates Osimertinib Resistance but is Sensitive to Neratinib and Poziotinib [J].
Castellano, Gina M. ;
Aisner, Joseph ;
Burley, Stephen K. ;
Vallat, Brinda ;
Yu, Helena A. ;
Pine, Sharon R. ;
Ganesan, Shridar .
JOURNAL OF THORACIC ONCOLOGY, 2019, 14 (11) :1982-1988
[16]   Co-activation of STAT3 and YES-Associated Protein 1 (YAP1) Pathway in EGFR-Mutant NSCLC [J].
Chaib, Imane ;
Karachaliou, Niki ;
Pilotto, Sara ;
Codony Servat, Jordi ;
Cai, Xueting ;
Li, Xuefei ;
Drozdowskyj, Ana ;
Codony Servat, Carles ;
Yang, Jie ;
Hu, Chunping ;
Felipe Cardona, Andres ;
Vivanco, Guillermo Lopez ;
Vergnenegre, Alain ;
Miguel Sanchez, Jose ;
Provencio, Mariano ;
de Marinis, Filippo ;
Passaro, Antonio ;
Carcereny, Enric ;
Reguart, Noemi ;
Garcia Campelo, Charo ;
Teixido, Cristina ;
Sperduti, Isabella ;
Rodriguez, Sonia ;
Lazzari, Chiara ;
Verlicchi, Alberto ;
de Aguirre, Itziar ;
Queralt, Cristina ;
Wei, Jia ;
Estrada, Roger ;
Puig de la Bellacasa, Raimon ;
Luis Ramirez, Jose ;
Jacobsen, Kirstine ;
Ditzel, Henrik J. ;
Santarpia, Mariacarmela ;
Viteri, Santiago ;
Angel Molina, Miguel ;
Zhou, Caicun ;
Cao, Peng ;
Ma, Patrick C. ;
Bivona, Trever G. ;
Rosell, Rafael .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2017, 109 (09)
[17]   Development of targeted protein degradation therapeutics [J].
Chamberlain, Philip P. ;
Hamann, Lawrence G. .
NATURE CHEMICAL BIOLOGY, 2019, 15 (10) :937-944
[18]   Antibody-drug conjugates for cancer [J].
Chau, Cindy H. ;
Steeg, Patricia S. ;
Figg, William D. .
LANCET, 2019, 394 (10200) :793-804
[19]   Crystal structure of aurora-2, an oncogenic serine/threonine kinase [J].
Cheetham, GMT ;
Knegtel, RMA ;
Coll, JT ;
Renwick, SB ;
Swenson, L ;
Weber, P ;
Lippke, JA ;
Austen, DA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (45) :42419-42422
[20]   Compound 15c, a Novel Dual Inhibitor of EGFRL858R/T790M and FGFR1, Efficiently Overcomes Epidermal Growth Factor Receptor-Tyrosine Kinase Inhibitor Resistance of Non-Small-Cell Lung Cancers [J].
Chen, Gaozhi ;
Bao, Yuyan ;
Weng, Qiaoyou ;
Zhao, Yingxin ;
Lu, Xiaoyao ;
Fu, Lili ;
Chen, Lingfeng ;
Liu, Zhiguo ;
Zhang, Xiaomin ;
Liang, Guang .
FRONTIERS IN PHARMACOLOGY, 2020, 10