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Analysis of different HER-2 mutations in breast cancer progression and drug resistance
- Source :
- Journal of Cellular and Molecular Medicine
- Publication Year :
- 2015
-
Abstract
- 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.
- Subjects :
- Receptor, ErbB-2
Reviews
Antineoplastic Agents
Breast Neoplasms
Drug resistance
Review
cancer risk
medicine.disease_cause
Bioinformatics
resistance
Breast cancer
breast cancer
Trastuzumab
medicine
HER‐2 mutation
Humans
Mutation
variants
Mechanism (biology)
business.industry
HER‐2
Lapatinib
Cell Biology
medicine.disease
Drug Resistance, Neoplasm
Disease Progression
Quinazolines
Molecular Medicine
Human epidermal growth factor receptor
Female
Carcinogenesis
Cancer risk
business
medicine.drug
Subjects
Details
- ISSN :
- 15824934
- Volume :
- 19
- Issue :
- 12
- Database :
- OpenAIRE
- Journal :
- Journal of cellular and molecular medicine
- Accession number :
- edsair.doi.dedup.....5a364882aacdfa1a5bc624375afad60d