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MicroRNA-125b reduces glucose uptake in papillary thyroid carcinoma cells

Previous studies have shown that microRNA (miR)-125b plays important roles in several human cancer types. The aim of the present study was to analyze the potential roles of miR-125b in papillary thyroid carcinoma (PTC). It was found that miR-125b was downregulated in PTC and its expression was affec...

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Detalles Bibliográficos
Autores principales: Zhang, Guowu, Zhou, Sihai, Yang, Quan, Liu, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7400998/
https://www.ncbi.nlm.nih.gov/pubmed/32782598
http://dx.doi.org/10.3892/ol.2020.11832
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author Zhang, Guowu
Zhou, Sihai
Yang, Quan
Liu, Fang
author_facet Zhang, Guowu
Zhou, Sihai
Yang, Quan
Liu, Fang
author_sort Zhang, Guowu
collection PubMed
description Previous studies have shown that microRNA (miR)-125b plays important roles in several human cancer types. The aim of the present study was to analyze the potential roles of miR-125b in papillary thyroid carcinoma (PTC). It was found that miR-125b was downregulated in PTC and its expression was affected by clinical stages. Glucose transporter 1 (GLUT1) was upregulated in PTC and was negatively correlated with miR-125b. In PTC cells, overexpression of miR-125b suppressed glucose uptake and downregulated GLUT1. Furthermore, GLUT1 overexpression reduced the effects of miR-125b overexpression on glucose uptake. Moreover, miR-125b overexpression suppressed PTC cell proliferation. GLUT1 overexpression promoted the proliferation of PTC cells and reduced the effects of miR-125b overexpression on cancer cell proliferation. Overall, miR-125b decreased glucose uptake in PTC cells by downregulating GLUT1.
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spelling pubmed-74009982020-08-10 MicroRNA-125b reduces glucose uptake in papillary thyroid carcinoma cells Zhang, Guowu Zhou, Sihai Yang, Quan Liu, Fang Oncol Lett Articles Previous studies have shown that microRNA (miR)-125b plays important roles in several human cancer types. The aim of the present study was to analyze the potential roles of miR-125b in papillary thyroid carcinoma (PTC). It was found that miR-125b was downregulated in PTC and its expression was affected by clinical stages. Glucose transporter 1 (GLUT1) was upregulated in PTC and was negatively correlated with miR-125b. In PTC cells, overexpression of miR-125b suppressed glucose uptake and downregulated GLUT1. Furthermore, GLUT1 overexpression reduced the effects of miR-125b overexpression on glucose uptake. Moreover, miR-125b overexpression suppressed PTC cell proliferation. GLUT1 overexpression promoted the proliferation of PTC cells and reduced the effects of miR-125b overexpression on cancer cell proliferation. Overall, miR-125b decreased glucose uptake in PTC cells by downregulating GLUT1. D.A. Spandidos 2020-09 2020-07-08 /pmc/articles/PMC7400998/ /pubmed/32782598 http://dx.doi.org/10.3892/ol.2020.11832 Text en Copyright: © Zhang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Zhang, Guowu
Zhou, Sihai
Yang, Quan
Liu, Fang
MicroRNA-125b reduces glucose uptake in papillary thyroid carcinoma cells
title MicroRNA-125b reduces glucose uptake in papillary thyroid carcinoma cells
title_full MicroRNA-125b reduces glucose uptake in papillary thyroid carcinoma cells
title_fullStr MicroRNA-125b reduces glucose uptake in papillary thyroid carcinoma cells
title_full_unstemmed MicroRNA-125b reduces glucose uptake in papillary thyroid carcinoma cells
title_short MicroRNA-125b reduces glucose uptake in papillary thyroid carcinoma cells
title_sort microrna-125b reduces glucose uptake in papillary thyroid carcinoma cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7400998/
https://www.ncbi.nlm.nih.gov/pubmed/32782598
http://dx.doi.org/10.3892/ol.2020.11832
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