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GPR30 regulates the EGFR-Akt cascade and predicts lower survival in patients with ovarian cancer

OBJECTIVES: G protein-coupled receptor 30 (GPR30) is a 7-transmembrane estrogen receptor that functions alongside traditional estrogen receptors to regulate the cellular responses to estrogen. Recent studies suggest that GPR30 expression is associated with a poor prognosis, and that this is due to t...

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Autores principales: Fujiwara, Satoe, Terai, Yoshito, Kawaguchi, Hiroshi, Takai, Masaaki, Yoo, Saha, Tanaka, Yoshimichi, Tanaka, Tomohito, Tsunetoh, Satoshi, Sasaki, Hiroshi, Kanemura, Masanori, Tanabe, Akiko, Yamashita, Yoshiki, Ohmichi, Masahide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3543193/
https://www.ncbi.nlm.nih.gov/pubmed/23163984
http://dx.doi.org/10.1186/1757-2215-5-35
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author Fujiwara, Satoe
Terai, Yoshito
Kawaguchi, Hiroshi
Takai, Masaaki
Yoo, Saha
Tanaka, Yoshimichi
Tanaka, Tomohito
Tsunetoh, Satoshi
Sasaki, Hiroshi
Kanemura, Masanori
Tanabe, Akiko
Yamashita, Yoshiki
Ohmichi, Masahide
author_facet Fujiwara, Satoe
Terai, Yoshito
Kawaguchi, Hiroshi
Takai, Masaaki
Yoo, Saha
Tanaka, Yoshimichi
Tanaka, Tomohito
Tsunetoh, Satoshi
Sasaki, Hiroshi
Kanemura, Masanori
Tanabe, Akiko
Yamashita, Yoshiki
Ohmichi, Masahide
author_sort Fujiwara, Satoe
collection PubMed
description OBJECTIVES: G protein-coupled receptor 30 (GPR30) is a 7-transmembrane estrogen receptor that functions alongside traditional estrogen receptors to regulate the cellular responses to estrogen. Recent studies suggest that GPR30 expression is associated with a poor prognosis, and that this is due to the GPR30-mediated transactivation of the EGFR in breast cancer. However, the biological contribution of GPR30 in ovarian cancer remains unclear. The purpose of this study was to elucidate the relationships between GPR30 expression and the clinicopathological findings, and to determine how the signaling cascade influences the prognosis of ovarian cancer. METHODS: The expression levels of GPR30, EGFR, ERα, and ERβ were analyzed using an immunohistochemical analysis, and their correlations with the clinicopathological features were examined in 10 patients with borderline malignant tumors and 152 patients with epithelial ovarian cancer. We also examined whether GPR30 signaling activates the EGFR-Akt pathway in an ovarian cancer cell line (Caov-3) by a Western blotting analysis. RESULTS: The GPR30 expression in ovarian carcinomas was significantly higher than that in borderline malignancies (p=0.0016), and was not associated with the expression of the EGFR, ERα, or ERβ. The expression of GPR30 in clear cell carcinomas was significantly lower than that in other subtypes of cancer (P <; 0.001). The expression of both GPR30 and EGFR was significantly associated with a poor prognosis in terms of the progression-free survival rate. The phosphorylation of the EGFR and Akt could be significantly enhanced by G1 (p <; 0.05) and inhibited by a Src family kinase inhibitor. CONCLUSION: The expression of both GPR30 and EGFR is associated with a poor outcome in ovarian cancer, and GPR30 increases the phosphorylation of Akt via the EGFR in ovarian cancer cells. The regulation of GPR30 might be a potentially useful new therapeutic target in ovarian cancer.
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spelling pubmed-35431932013-01-14 GPR30 regulates the EGFR-Akt cascade and predicts lower survival in patients with ovarian cancer Fujiwara, Satoe Terai, Yoshito Kawaguchi, Hiroshi Takai, Masaaki Yoo, Saha Tanaka, Yoshimichi Tanaka, Tomohito Tsunetoh, Satoshi Sasaki, Hiroshi Kanemura, Masanori Tanabe, Akiko Yamashita, Yoshiki Ohmichi, Masahide J Ovarian Res Research OBJECTIVES: G protein-coupled receptor 30 (GPR30) is a 7-transmembrane estrogen receptor that functions alongside traditional estrogen receptors to regulate the cellular responses to estrogen. Recent studies suggest that GPR30 expression is associated with a poor prognosis, and that this is due to the GPR30-mediated transactivation of the EGFR in breast cancer. However, the biological contribution of GPR30 in ovarian cancer remains unclear. The purpose of this study was to elucidate the relationships between GPR30 expression and the clinicopathological findings, and to determine how the signaling cascade influences the prognosis of ovarian cancer. METHODS: The expression levels of GPR30, EGFR, ERα, and ERβ were analyzed using an immunohistochemical analysis, and their correlations with the clinicopathological features were examined in 10 patients with borderline malignant tumors and 152 patients with epithelial ovarian cancer. We also examined whether GPR30 signaling activates the EGFR-Akt pathway in an ovarian cancer cell line (Caov-3) by a Western blotting analysis. RESULTS: The GPR30 expression in ovarian carcinomas was significantly higher than that in borderline malignancies (p=0.0016), and was not associated with the expression of the EGFR, ERα, or ERβ. The expression of GPR30 in clear cell carcinomas was significantly lower than that in other subtypes of cancer (P <; 0.001). The expression of both GPR30 and EGFR was significantly associated with a poor prognosis in terms of the progression-free survival rate. The phosphorylation of the EGFR and Akt could be significantly enhanced by G1 (p <; 0.05) and inhibited by a Src family kinase inhibitor. CONCLUSION: The expression of both GPR30 and EGFR is associated with a poor outcome in ovarian cancer, and GPR30 increases the phosphorylation of Akt via the EGFR in ovarian cancer cells. The regulation of GPR30 might be a potentially useful new therapeutic target in ovarian cancer. BioMed Central 2012-11-19 /pmc/articles/PMC3543193/ /pubmed/23163984 http://dx.doi.org/10.1186/1757-2215-5-35 Text en Copyright ©2012 Fujiwara et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Fujiwara, Satoe
Terai, Yoshito
Kawaguchi, Hiroshi
Takai, Masaaki
Yoo, Saha
Tanaka, Yoshimichi
Tanaka, Tomohito
Tsunetoh, Satoshi
Sasaki, Hiroshi
Kanemura, Masanori
Tanabe, Akiko
Yamashita, Yoshiki
Ohmichi, Masahide
GPR30 regulates the EGFR-Akt cascade and predicts lower survival in patients with ovarian cancer
title GPR30 regulates the EGFR-Akt cascade and predicts lower survival in patients with ovarian cancer
title_full GPR30 regulates the EGFR-Akt cascade and predicts lower survival in patients with ovarian cancer
title_fullStr GPR30 regulates the EGFR-Akt cascade and predicts lower survival in patients with ovarian cancer
title_full_unstemmed GPR30 regulates the EGFR-Akt cascade and predicts lower survival in patients with ovarian cancer
title_short GPR30 regulates the EGFR-Akt cascade and predicts lower survival in patients with ovarian cancer
title_sort gpr30 regulates the egfr-akt cascade and predicts lower survival in patients with ovarian cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3543193/
https://www.ncbi.nlm.nih.gov/pubmed/23163984
http://dx.doi.org/10.1186/1757-2215-5-35
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