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A review of the use of next generation sequencing methodologies to identify biomarkers of resistance to CDK4/6 inhibitors in ER+/HER2- breast cancer
- Source :
- Critical reviews in oncology/hematology. 157
- Publication Year :
- 2020
-
Abstract
- The development of cyclin-dependent kinases (CDK) 4 and 6 inhibitors represented a substantial breakthrough in the treatment of estrogen receptor positive (ER+), human epidermal growth factor receptor 2 (HER2) negative metastatic breast cancer. These drugs showed a significant clinical benefit in pivotal clinical trials. However, resistance eventually occurs, leading to disease progression. Next Generation Sequencing methodologies have been employed to investigate predictive biomarkers of response or resistance to CDK4/6 inhibitors. Whole exome and targeted sequencing of solid and liquid biopsies have revealed several possible genomic alterations associated with resistance. Notably, genomic alterations identified by DNA-sequencing did not fully recapitulate the entire landscape of resistance to CDK4/6 inhibitors. Gene expression analysis, such as RNA-Seq methodologies, have provided insights into transcriptional profiles and may need further application. Herein, we report the main findings derived from the use of NGS analysis in the context of resistance to CDK4/6 inhibitors in ER + breast cancer.
- Subjects :
- 0301 basic medicine
Estrogen receptor
Protein Kinase Inhibitor
Context (language use)
Breast Neoplasms
DNA sequencing
CDK4/6 inhibitor
03 medical and health sciences
0302 clinical medicine
Breast cancer
Cyclin-dependent kinase
Next generation sequencing
medicine
Humans
Exome
Protein Kinase Inhibitors
biology
business.industry
Precision medicine
Cyclin-Dependent Kinase 4
High-Throughput Nucleotide Sequencing
Hematology
Cyclin-Dependent Kinase 6
Genomics
medicine.disease
Metastatic breast cancer
030104 developmental biology
Oncology
030220 oncology & carcinogenesis
biology.protein
Cancer research
Genomic
business
Human
Subjects
Details
- ISSN :
- 18790461
- Volume :
- 157
- Database :
- OpenAIRE
- Journal :
- Critical reviews in oncology/hematology
- Accession number :
- edsair.doi.dedup.....6b8d4e8ad139c7ecee17abf5dd2f2239