Abstract

Human chorionic gonadotropin (hCG) is a hormone that specifically binds to luteinizing hormone receptor (LHR) and exerts several roles, including the support of pregnancy and fetal gonadal steroidogenesis. Since hCG is also expressed by some tumor types, like breast cancer, many efforts have been made to study its role in neoplesia, with some studies showing a cancer-supportive role and others showing a cancer-protective role. A critical examination of the literature highlighted that the in vitro effect of hCG has been tested in the presence of fetal serum, which contains other gonadotropins, in the culture medium. Thus, we hypothesized that the use of serum in the cell culture medium might influence the cell response to the hCG treatment due to the presence of other hormones. Thus, we analyzed the in vitro effect of highly purified hCG on cell proliferation and the activation of the down-stream signal transduction pathway in three breast cancer cell lines, particularly focusing on MCF7, cultured in serum-deprived conditions. Our data show that hCG increases cell proliferation and activates the down-stream target Akt, together with a decrease of the LHR mRNA expression level. Finally, we also tested the differentiation capacity of hCG on MCF7 cancer stem cells (CSCs) and show that it favors the proliferation and differentiation of these cells, thus suggesting that hCG also renders cells more able to colonize and invade the organs.

Highlights

  • Human chorionic gonadotropin is a glycoprotein hormone that belongs to the gonadotropin hormone family, which includes luteinizing hormone (LH) and folliclestimulating hormone (FSH). hCG is a heterodimeric protein with two subunits: the alphasubunit that is identical to that of LH, FSH, and thyroid-stimulating hormone (TSH), and the beta-subunit that is specific to hCG alone

  • These hormones bind to specific G proteincoupled receptors (GPCRs): LH and hCG bind to luteinizing hormone receptor (LHR), whereas FSH binds to follicle-stimulating hormone receptor (FSHR)

  • In order to study the effect of human chorionic gonadotropin on breast cancer cells, we firstly analyzed the expression of the hCG-specific receptor LHR through confocal microscopy in MCF7 cells in comparison to the control cell line PaCa44, which does not express LHR due to its origin, i.e., pancreatic ductal adenocarcinoma

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Summary

Introduction

Human chorionic gonadotropin (hCG) is a glycoprotein hormone that belongs to the gonadotropin hormone family, which includes luteinizing hormone (LH) and folliclestimulating hormone (FSH). hCG is a heterodimeric protein with two subunits: the alphasubunit that is identical to that of LH, FSH, and thyroid-stimulating hormone (TSH), and the beta-subunit that is specific to hCG alone. HCG is a heterodimeric protein with two subunits: the alphasubunit that is identical to that of LH, FSH, and thyroid-stimulating hormone (TSH), and the beta-subunit that is specific to hCG alone. These hormones bind to specific G proteincoupled receptors (GPCRs): LH and hCG bind to luteinizing hormone receptor (LHR), whereas FSH binds to follicle-stimulating hormone receptor (FSHR). Instead, concerning the pro-tumorigenic role of hCG, it has been shown that some tumors, including breast, bladder, and testicular cancer [11,12], express this hormone at high levels, making it a potential tumor marker and a tool to monitor disease progression [13]. In vitro studies showed that β-hCG promotes cancer cell invasion in different types of tumors [15,16]

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