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Cross-talk between GPER and growth factor signaling

The Journal of Steroid Biochemistry and Molecular BiologyPublished 28 March 2013
Rosamaria Lappano, Paola De Marco, Ernestina Marianna De Francesco, Adele Chimento, Vincenzo Pezzi, Marcello Maggiolini
Citations87
SJR quartileQ2
SJR score0.73
SNIP0.76

TL;DR

This review highlights recent findings on the cross-talk between a member of the GPCR family, the G protein-coupled estrogen receptor 1 (GPER), and two main growth factor receptors like EGFR and insulin-like growth factor-I receptor (IGF-IR).

Abstract

G protein-coupled receptors (GPCRs) and growth factor receptors mediate multiple physio-pathological responses to a diverse array of extracellular stimuli. In this regard, it has been largely demonstrated that GPCRs and growth factor receptors generate a multifaceted signaling network, which triggers relevant biological effects in normal and cancer cells. For instance, some GPCRs transactivate the epidermal growth factor receptor (EGFR), which stimulates diverse transduction pathways leading to gene expression changes, cell migration, survival and proliferation. Moreover, it has been reported that a functional interaction between growth factor receptors and steroid hormones like estrogens is involved in the growth of many types of tumors as well as in the resistance to endocrine therapy. This review highlights recent findings on the cross-talk between a member of the GPCR family, the G protein-coupled estrogen receptor 1 (GPER, formerly known as GPR30) and two main growth factor receptors like EGFR and insulin-like growth factor-I receptor (IGF-IR). The biological implications of the functional interaction between these important mediators of cell responses particularly in cancer are discussed. This article is part of a Special Issue entitled 'CSR 2013'.

Keywords

Biochemistry, Genetics and Molecular Biology