EGFR mutation mediates resistance to EGFR tyrosine kinase inhibitors in NSCLC: From molecular mechanisms to clinical research

被引:136
作者
Dong, Rui-Fang [1 ,2 ]
Zhu, Miao-Lin [3 ]
Liu, Ming-Ming [1 ,2 ]
Xu, Yi-Ting [1 ,2 ]
Yuan, Liu-Liu [1 ,2 ]
Bian, Jing [1 ,2 ]
Xia, Yuan-Zheng [1 ,2 ,4 ]
Kong, Ling-Yi [1 ,2 ]
机构
[1] China Pharmaceut Univ, Sch Tradit Chinese Pharm, Jiangsu Key Lab Bioact Nat Prod Res, 24 Tong Jia Xiang, Nanjing 210009, Peoples R China
[2] China Pharmaceut Univ, Sch Tradit Chinese Pharm, State Key Lab Nat Med, 24 Tong Jia Xiang, Nanjing 210009, Peoples R China
[3] Jiangsu Canc Hosp, Dept Pathol, Nanjing 210009, Peoples R China
[4] Guangxi Med Univ, Minist Educ, Key Lab High Incidence Tumour Prevent & Treatment, Nanning 530021, Peoples R China
基金
中国国家自然科学基金;
关键词
EGFR mutations; NSCLC; EGFR-TKI resistance; Overcoming drug resistance; Future development; CELL LUNG-CANCER; GROWTH-FACTOR RECEPTOR; AFATINIB PLUS CETUXIMAB; EXON; 20; INSERTIONS; ACQUIRED-RESISTANCE; T790M MUTATION; BISPECIFIC ANTIBODY; TUMOR-CELLS; ERLOTINIB RESISTANCE; PROTEIN-DEGRADATION;
D O I
10.1016/j.phrs.2021.105583
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
With the development of precision medicine, molecular targeted therapy has been widely used in the field of cancer, especially in non-small-cell lung cancer (NSCLC). Epidermal growth factor receptor (EGFR) is a well-recognized and effective target for NSCLC therapies, targeted EGFR therapy with EGFR-tyrosine kinase inhibitors (EGFR-TKIs) has achieved ideal clinical efficacy in recent years. Unfortunately, resistance to EGFR-TKIs inevitably occurs due to various mechanisms after a period of therapy. EGFR mutations, such as T790M and C797S, are the most common mechanism of EGFR-TKI resistance. Here, we discuss the mechanisms of EGFR-TKIs resistance induced by secondary EGFR mutations, highlight the development of targeted drugs to overcome EGFR mutation-mediated resistance, and predict the promising directions for development of novel candidates.
引用
收藏
页数:18
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