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MicroRNA-4728 mediated regulation of MAPK oncogenic signaling in papillary thyroid carcinoma

Papillary thyroid carcinoma (PTC) is the most common type of thyroid cancer that accounts for 85% of thyroid cancers. MicroRNAs (miRNAs) have been reported to play important roles in the biological processes in cancer. In this study, we analyzed the biological role of miR-4728 in human PTC process i...

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Detalles Bibliográficos
Autores principales: Liu, Zhibao, Zhang, Jinghua, Gao, Jinghua, Li, Yunnan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6088101/
https://www.ncbi.nlm.nih.gov/pubmed/30108452
http://dx.doi.org/10.1016/j.sjbs.2018.05.014
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author Liu, Zhibao
Zhang, Jinghua
Gao, Jinghua
Li, Yunnan
author_facet Liu, Zhibao
Zhang, Jinghua
Gao, Jinghua
Li, Yunnan
author_sort Liu, Zhibao
collection PubMed
description Papillary thyroid carcinoma (PTC) is the most common type of thyroid cancer that accounts for 85% of thyroid cancers. MicroRNAs (miRNAs) have been reported to play important roles in the biological processes in cancer. In this study, we analyzed the biological role of miR-4728 in human PTC process in human PTC cell lines in vitro. MiRNA-4728 was observed to down-regulated in human PTC tissues and PTC cell lines. Additionally, miR-4728 inhibited PTC cell proliferation. Further study demonstrated SOS1 was repressed by miR-4728 and overexpression of miR-4728 down-regulated both the mRNA and protein levels of SOS1. Moreover, miR-4728 overexpression also decreased the MAPK signaling activity. These observations suggested that miR-4728 could inhibit the process of human PTC through regulating MAPK signaling pathway. And, appropriate regulation of miR-4728 might be vital to improve human PTC treatment.
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spelling pubmed-60881012018-08-14 MicroRNA-4728 mediated regulation of MAPK oncogenic signaling in papillary thyroid carcinoma Liu, Zhibao Zhang, Jinghua Gao, Jinghua Li, Yunnan Saudi J Biol Sci Article Papillary thyroid carcinoma (PTC) is the most common type of thyroid cancer that accounts for 85% of thyroid cancers. MicroRNAs (miRNAs) have been reported to play important roles in the biological processes in cancer. In this study, we analyzed the biological role of miR-4728 in human PTC process in human PTC cell lines in vitro. MiRNA-4728 was observed to down-regulated in human PTC tissues and PTC cell lines. Additionally, miR-4728 inhibited PTC cell proliferation. Further study demonstrated SOS1 was repressed by miR-4728 and overexpression of miR-4728 down-regulated both the mRNA and protein levels of SOS1. Moreover, miR-4728 overexpression also decreased the MAPK signaling activity. These observations suggested that miR-4728 could inhibit the process of human PTC through regulating MAPK signaling pathway. And, appropriate regulation of miR-4728 might be vital to improve human PTC treatment. Elsevier 2018-07 2018-05-09 /pmc/articles/PMC6088101/ /pubmed/30108452 http://dx.doi.org/10.1016/j.sjbs.2018.05.014 Text en © 2018 Production and hosting by Elsevier B.V. on behalf of King Saud University. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Liu, Zhibao
Zhang, Jinghua
Gao, Jinghua
Li, Yunnan
MicroRNA-4728 mediated regulation of MAPK oncogenic signaling in papillary thyroid carcinoma
title MicroRNA-4728 mediated regulation of MAPK oncogenic signaling in papillary thyroid carcinoma
title_full MicroRNA-4728 mediated regulation of MAPK oncogenic signaling in papillary thyroid carcinoma
title_fullStr MicroRNA-4728 mediated regulation of MAPK oncogenic signaling in papillary thyroid carcinoma
title_full_unstemmed MicroRNA-4728 mediated regulation of MAPK oncogenic signaling in papillary thyroid carcinoma
title_short MicroRNA-4728 mediated regulation of MAPK oncogenic signaling in papillary thyroid carcinoma
title_sort microrna-4728 mediated regulation of mapk oncogenic signaling in papillary thyroid carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6088101/
https://www.ncbi.nlm.nih.gov/pubmed/30108452
http://dx.doi.org/10.1016/j.sjbs.2018.05.014
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