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The root cause of drug resistance in HER2-positive breast cancer and the therapeutic approaches to overcoming the resistance
- Source :
- Pharmacol Ther
- Publication Year :
- 2021
- Publisher :
- Elsevier BV, 2021.
-
Abstract
- HER2 is a well-known oncogenic receptor tyrosine kinase. HER2 gene amplification occurs in about 20% of breast cancer (BC), which leads to overexpression of HER2 protein, known as HER2-positive BC. Inhibitors of HER2 have significantly improved the prognosis of patients with this subset of BC. Since 1998, seven HER2 inhibitors have been developed to treat this disease. However, drug resistance is common and remains a major unresolved clinical problem. Patients typically show disease progression after some time on treatment. This review discusses the complexity and diversified nature of HER2 signaling, the mechanisms of actions and therapeutic activities of all HER2 inhibitors, the roles of HER2 and other signaling proteins in HER2-positive BC resistant to the inhibitors, the non-cell-autonomous mechanisms of drug resistance, and the heterogeneity of tumor HER2 expression. The review presents the concept that drug resistance in HER2-positive BC results primarily from the inability of HER2 inhibitors to deplete HER2. Emerging therapeutics that are promising for overcoming drug resistance are also discussed.
- Subjects :
- 0301 basic medicine
Time on treatment
medicine.medical_treatment
Antineoplastic Agents
Breast Neoplasms
Disease
Drug resistance
Article
Receptor tyrosine kinase
Targeted therapy
03 medical and health sciences
0302 clinical medicine
Breast cancer
HER2 Positive Breast Cancer
medicine
Humans
Pharmacology (medical)
skin and connective tissue diseases
neoplasms
Pharmacology
Her2 expression
biology
business.industry
Oncogenes
medicine.disease
030104 developmental biology
Drug Resistance, Neoplasm
030220 oncology & carcinogenesis
biology.protein
Cancer research
Female
business
Subjects
Details
- ISSN :
- 01637258
- Volume :
- 218
- Database :
- OpenAIRE
- Journal :
- Pharmacology & Therapeutics
- Accession number :
- edsair.doi.dedup.....f5f870216476c7bc77f977c40f5bb5e4
- Full Text :
- https://doi.org/10.1016/j.pharmthera.2020.107677