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MiR-106b promotes cell proliferation via targeting RB in laryngeal carcinoma

MiR-106b is frequently up-regulated in various types of human cancer including laryngeal carcinoma. However the underlying mechanism of miR-106b involved in laryngeal carcinoma remains elusive. Here we showed that reduction of miR-106b induced cell cycle G0/G1 arrest by targeting tumor suppressor RB...

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Detalles Bibliográficos
Autores principales: Cai, Kemin, Wang, Yu, Bao, Xueli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3161894/
https://www.ncbi.nlm.nih.gov/pubmed/21819631
http://dx.doi.org/10.1186/1756-9966-30-73
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author Cai, Kemin
Wang, Yu
Bao, Xueli
author_facet Cai, Kemin
Wang, Yu
Bao, Xueli
author_sort Cai, Kemin
collection PubMed
description MiR-106b is frequently up-regulated in various types of human cancer including laryngeal carcinoma. However the underlying mechanism of miR-106b involved in laryngeal carcinoma remains elusive. Here we showed that reduction of miR-106b induced cell cycle G0/G1 arrest by targeting tumor suppressor RB in human laryngeal carcinoma cells. Further, Introducing RB cDNA without 3'UTR abrogated miR-106b-induced cell proliferation. Finally, there was an inverse relationship between RB and miR-106b expression in laryngeal carcinoma tissues. To our knowledge, these data indicate for the first time that miR-106b directly regulate cell cycle by targeting RB in laryngeal carcinoma and that miR-106b could be potential therapeutic approaches for laryngeal carcinoma.
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spelling pubmed-31618942011-08-26 MiR-106b promotes cell proliferation via targeting RB in laryngeal carcinoma Cai, Kemin Wang, Yu Bao, Xueli J Exp Clin Cancer Res Research MiR-106b is frequently up-regulated in various types of human cancer including laryngeal carcinoma. However the underlying mechanism of miR-106b involved in laryngeal carcinoma remains elusive. Here we showed that reduction of miR-106b induced cell cycle G0/G1 arrest by targeting tumor suppressor RB in human laryngeal carcinoma cells. Further, Introducing RB cDNA without 3'UTR abrogated miR-106b-induced cell proliferation. Finally, there was an inverse relationship between RB and miR-106b expression in laryngeal carcinoma tissues. To our knowledge, these data indicate for the first time that miR-106b directly regulate cell cycle by targeting RB in laryngeal carcinoma and that miR-106b could be potential therapeutic approaches for laryngeal carcinoma. BioMed Central 2011-08-08 /pmc/articles/PMC3161894/ /pubmed/21819631 http://dx.doi.org/10.1186/1756-9966-30-73 Text en Copyright ©2011 Cai 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
Cai, Kemin
Wang, Yu
Bao, Xueli
MiR-106b promotes cell proliferation via targeting RB in laryngeal carcinoma
title MiR-106b promotes cell proliferation via targeting RB in laryngeal carcinoma
title_full MiR-106b promotes cell proliferation via targeting RB in laryngeal carcinoma
title_fullStr MiR-106b promotes cell proliferation via targeting RB in laryngeal carcinoma
title_full_unstemmed MiR-106b promotes cell proliferation via targeting RB in laryngeal carcinoma
title_short MiR-106b promotes cell proliferation via targeting RB in laryngeal carcinoma
title_sort mir-106b promotes cell proliferation via targeting rb in laryngeal carcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3161894/
https://www.ncbi.nlm.nih.gov/pubmed/21819631
http://dx.doi.org/10.1186/1756-9966-30-73
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AT baoxueli mir106bpromotescellproliferationviatargetingrbinlaryngealcarcinoma