G protein-coupled receptors (GPCRs) represent the largest family of druggable targets in human genome. Although several GPCRs can cross-talk with the human epidermal growth factor receptors (HERs), the expression and function of most GPCRs remain unknown in HER2+ breast cancer (BC). In this study, we aimed to evaluate gene expression of GPCRs in tumorigenic or anti-HER2 drug-resistant cells and to understand the potential role of candidate GPCRs in HER2+ BC.

GPCRs profiling and identification of GPR110 as a potential new target in HER2+ breast cancer

De Angelis C.;
2018-01-01

Abstract

G protein-coupled receptors (GPCRs) represent the largest family of druggable targets in human genome. Although several GPCRs can cross-talk with the human epidermal growth factor receptors (HERs), the expression and function of most GPCRs remain unknown in HER2+ breast cancer (BC). In this study, we aimed to evaluate gene expression of GPCRs in tumorigenic or anti-HER2 drug-resistant cells and to understand the potential role of candidate GPCRs in HER2+ BC.
2018
Breast cancer
Drug resistance
Drug targets
GPR110
HER2
Tumorigenesis
Animals
Antineoplastic Agents
Breast Neoplasms
Cell Line
Tumor
Cell Proliferation
Disease Models
Animal
Drug Resistance
Neoplasm
Female
Gene Knockdown Techniques
Humans
Mice
Molecular Targeted Therapy
Oncogene Proteins
RNA
Small Interfering
Receptor
ErbB-2
Receptors
G-Protein-Coupled
Reproducibility of Results
Xenograft Model Antitumor Assays
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14246/1696
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