Analysis of different HER-2 mutations in breast cancer progression and drug resistance

被引:51
作者
Sun, Zijia [1 ]
Shi, Yaqin [1 ]
Shen, Yan [1 ]
Cao, Lulu [1 ]
Zhang, Wenwen [1 ]
Guan, Xiaoxiang [1 ,2 ]
机构
[1] Nanjing Univ, Sch Med, Jinling Hosp, Dept Med Oncol, Nanjing 210008, Jiangsu, Peoples R China
[2] Southern Med Univ, Sch Med, Jinling Hosp, Dept Med Oncol, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
breast cancer; HER-2; mutation; variants; cancer risk; resistance; GROWTH-FACTOR RECEPTOR; CELL LUNG-CANCER; TYROSINE KINASE INHIBITORS; CARBOXY-TERMINAL FRAGMENT; GENE AMPLIFICATION; SOMATIC MUTATIONS; ACTIVATING MUTATIONS; ACQUIRED-RESISTANCE; PROTEIN EXPRESSION; CODON-655; POLYMORPHISM;
D O I
10.1111/jcmm.12662
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Studies over the last two decades have identified that amplified human epidermal growth factor receptor (HER-2; c-erbB-2, neu) and its overexpression have been frequently implicated in the carcinogenesis and prognosis in a variety of solid tumours, especially breast cancer. Lots of painstaking efforts were invested on the HER-2 targeted agents, and significantly improved outcome and prolonged the survival of patients. However, some patients classified as 'HER-2-positive' would be still resistant to the anti-HER-2 therapy. Various mechanisms of drug resistance have been illustrated and the alteration of HER-2 was considered as a crucial mechanism. However, systematic researches in regard to the HER-2 mutations and variants are still inadequate. Notably, the alterations of HER-2 play an important role in drug resistance, but also have a potential association with the cancer risk. In this review, we summarize the possible mutations and focus on HER-2 variants' role in breast cancer tumourigenesis. Additionally, the alteration of HER-2, as a potential mechanism of resistance to trastuzumab, is discussed here. We hope that HER-2 related activating mutations could potentially offer more therapeutic opportunities to a broader range of patients than previously classified as HER-2 overexpressed.
引用
收藏
页码:2691 / 2701
页数:11
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