G-protein coupled receptor 64 (GPR64) acts as a tumor suppressor in endometrial cancer.

Abstract

BACKGROUND:

Endometrial cancer is the most common gynecological cancer. G-protein coupled receptor 64 (GPR64) belongs to a family of adhesion GPCRs and plays an important role in male fertility. However, the function of GPR64 has not been studied in endometrial cancer. Our objective is to investigate the role of GPR64 in endometrial cancer.

METHODS:

We examined the levels of GPR64 in human endometrioid endometrial carcinoma by immunohistochemistry analysis. To determine a tumor suppressor role of GPR64 in endometrial cancer, we used a siRNA loss of function approach in human endometrial adenocarcinoma cell lines.

RESULTS:

GPR64 levels were remarkably lower in 10 of 21 (47.62%) of endometrial carcinoma samples compared to control. Depletion of GPR64 by siRNA transfection revealed an increase of colony formation ability, cell proliferation, cell migration, and invasion activity in Ishikawa and HEC1A cells. The expression of Connexin 43 (Cx43), a member of the large family of gap junction proteins, was reduced through activation of AMP-activated protein kinase (AMPK) in Ishikawa cells with GPR64-deficicy.

CONCLUSIONS:

These results suggest that GPR64 plays an important tumor suppressor role in endometrial cancer.

• Authors: Jong Il Ahn, Jung-Yoon Yoo, Tae Hoon Kim, Young Im Kim, Russell R Broaddus, Ji Yeon Ahn, Jeong Mook Lim, Jae-Wook Jeong
• Journal: BMC cancer (BMC Cancer) Vol. 19 Issue 1 Pg. 810 (Aug 14 2019) ISSN: 1471-2407 [Electronic] England
• PMID: 31412816 (Publication Type: Journal Article)

Chemical References

• ADGRG2 protein, human
• Connexin 43
• GJA1 protein, human
• RNA, Small Interfering
• Receptors, G-Protein-Coupled
• AMP-Activated Protein Kinases

Topics

• AMP-Activated Protein Kinases (metabolism)
• Carcinoma, Endometrioid (genetics, metabolism, pathology)
• Cell Line, Tumor
• Cell Movement
• Cell Proliferation
• Connexin 43 (metabolism)
• Endometrial Neoplasms (genetics, metabolism, pathology)
• Female
• Gene Expression Regulation, Neoplastic
• Humans
• Neoplasm Invasiveness
• Phosphorylation
• RNA, Small Interfering
• Receptors, G-Protein-Coupled (antagonists & inhibitors, genetics, metabolism)