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The effects of PGC-1α on the proliferation and energy metabolism of malignant endometrial cancer cells

BACKGROUND: It is well known that peroxisome proliferator-activated receptor gamma coactivator-1 alpha (PGC-1α) plays an important role in tissue energy metabolism. However, the roles of PGC-1α in malignant endometrial cancer remain unknown. METHODS: Forty cases of endometrial carcinoma, 15 cases wi...

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Autores principales: Ren, Zhongqian, Yang, Hui, Wang, Cuicui, Ma, Xiaoxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4399546/
https://www.ncbi.nlm.nih.gov/pubmed/25914546
http://dx.doi.org/10.2147/OTT.S79960
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author Ren, Zhongqian
Yang, Hui
Wang, Cuicui
Ma, Xiaoxin
author_facet Ren, Zhongqian
Yang, Hui
Wang, Cuicui
Ma, Xiaoxin
author_sort Ren, Zhongqian
collection PubMed
description BACKGROUND: It is well known that peroxisome proliferator-activated receptor gamma coactivator-1 alpha (PGC-1α) plays an important role in tissue energy metabolism. However, the roles of PGC-1α in malignant endometrial cancer remain unknown. METHODS: Forty cases of endometrial carcinoma, 15 cases with proliferative endometrial tissues, and 21 cases with normal endometrial tissues were collected. Real-time polymerase chain reaction was used to detect the mRNA levels of PGC-1α and estrogen-related receptor gamma (ERRγ). ELISA (enzyme-linked immunosorbent assay) was used to detect the concentrations of pyruvate kinase and isocitrate dehydrogenase. The results were analyzed using medical statistical methods. RESULTS: The mRNA levels of PGC-1α and ERRγ in the endometrial carcinoma tissues and hyperplasic endometrial tissues were significantly greater than those in the normal endometria. The mRNA levels of PGC-1α and ERRγ in the endometrial carcinoma patients with type 2 diabetes were higher than those in patients without diabetes. The mRNA levels of PGC-1α and ERRγ in the endometrial adenocarcinomas increased with clinical staging, depth of myometrial invasion, and increases in the number of metastatic lymph nodes. The PGC-1α mRNA level was positively correlated with ERRγ in the endometrial carcinoma tissues. The mRNA levels of PGC-1α were positively correlated with the concentrations of pyruvate kinase and isocitrate dehydrogenase in the endometrial carcinoma tissues, and similar results were found for ERRγ. CONCLUSION: Our results suggested that the upregulation of PGC-1α and ERRγ in endometrial cancer might be a requirement for cancer cell energy metabolism, which contributes to the development of endometrial cancer.
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spelling pubmed-43995462015-04-24 The effects of PGC-1α on the proliferation and energy metabolism of malignant endometrial cancer cells Ren, Zhongqian Yang, Hui Wang, Cuicui Ma, Xiaoxin Onco Targets Ther Original Research BACKGROUND: It is well known that peroxisome proliferator-activated receptor gamma coactivator-1 alpha (PGC-1α) plays an important role in tissue energy metabolism. However, the roles of PGC-1α in malignant endometrial cancer remain unknown. METHODS: Forty cases of endometrial carcinoma, 15 cases with proliferative endometrial tissues, and 21 cases with normal endometrial tissues were collected. Real-time polymerase chain reaction was used to detect the mRNA levels of PGC-1α and estrogen-related receptor gamma (ERRγ). ELISA (enzyme-linked immunosorbent assay) was used to detect the concentrations of pyruvate kinase and isocitrate dehydrogenase. The results were analyzed using medical statistical methods. RESULTS: The mRNA levels of PGC-1α and ERRγ in the endometrial carcinoma tissues and hyperplasic endometrial tissues were significantly greater than those in the normal endometria. The mRNA levels of PGC-1α and ERRγ in the endometrial carcinoma patients with type 2 diabetes were higher than those in patients without diabetes. The mRNA levels of PGC-1α and ERRγ in the endometrial adenocarcinomas increased with clinical staging, depth of myometrial invasion, and increases in the number of metastatic lymph nodes. The PGC-1α mRNA level was positively correlated with ERRγ in the endometrial carcinoma tissues. The mRNA levels of PGC-1α were positively correlated with the concentrations of pyruvate kinase and isocitrate dehydrogenase in the endometrial carcinoma tissues, and similar results were found for ERRγ. CONCLUSION: Our results suggested that the upregulation of PGC-1α and ERRγ in endometrial cancer might be a requirement for cancer cell energy metabolism, which contributes to the development of endometrial cancer. Dove Medical Press 2015-04-09 /pmc/articles/PMC4399546/ /pubmed/25914546 http://dx.doi.org/10.2147/OTT.S79960 Text en © 2015 Ren et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Ren, Zhongqian
Yang, Hui
Wang, Cuicui
Ma, Xiaoxin
The effects of PGC-1α on the proliferation and energy metabolism of malignant endometrial cancer cells
title The effects of PGC-1α on the proliferation and energy metabolism of malignant endometrial cancer cells
title_full The effects of PGC-1α on the proliferation and energy metabolism of malignant endometrial cancer cells
title_fullStr The effects of PGC-1α on the proliferation and energy metabolism of malignant endometrial cancer cells
title_full_unstemmed The effects of PGC-1α on the proliferation and energy metabolism of malignant endometrial cancer cells
title_short The effects of PGC-1α on the proliferation and energy metabolism of malignant endometrial cancer cells
title_sort effects of pgc-1α on the proliferation and energy metabolism of malignant endometrial cancer cells
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4399546/
https://www.ncbi.nlm.nih.gov/pubmed/25914546
http://dx.doi.org/10.2147/OTT.S79960
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