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MicroRNA-361-5p suppresses cancer progression by targeting signal transducer and activator of transcription 6 in non-small cell lung cancer

The incidence of non-small cell lung cancer (NSCLC) has significantly increased in China, while the prognosis of affected patients is poor. The pathogenesis of NSCLC is thought to be regulated by microRNAs (miRs). The present study used a miR array in order to determine the expression of miR-361-5p,...

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Autores principales: MA, YUEFENG, BAO, CHUANEN, KONG, RANRAN, XING, XIN, ZHANG, YAYA, LI, SHAOMIN, ZHANG, WEI, JIANG, JIANTAO, ZHANG, JIN, QIAO, ZHE, ZHANG, DANJIE, MA, ZHENCHUAN, SUN, LIANGZHANG, ZHOU, BIN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626161/
https://www.ncbi.nlm.nih.gov/pubmed/26461141
http://dx.doi.org/10.3892/mmr.2015.4411
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author MA, YUEFENG
BAO, CHUANEN
KONG, RANRAN
XING, XIN
ZHANG, YAYA
LI, SHAOMIN
ZHANG, WEI
JIANG, JIANTAO
ZHANG, JIN
QIAO, ZHE
ZHANG, DANJIE
MA, ZHENCHUAN
SUN, LIANGZHANG
ZHOU, BIN
author_facet MA, YUEFENG
BAO, CHUANEN
KONG, RANRAN
XING, XIN
ZHANG, YAYA
LI, SHAOMIN
ZHANG, WEI
JIANG, JIANTAO
ZHANG, JIN
QIAO, ZHE
ZHANG, DANJIE
MA, ZHENCHUAN
SUN, LIANGZHANG
ZHOU, BIN
author_sort MA, YUEFENG
collection PubMed
description The incidence of non-small cell lung cancer (NSCLC) has significantly increased in China, while the prognosis of affected patients is poor. The pathogenesis of NSCLC is thought to be regulated by microRNAs (miRs). The present study used a miR array in order to determine the expression of miR-361-5p, which was significantly lower in NSCLC tissues compared with that in adjacent tissues, indicating a crucial role of miR-361-5p during the progression of NSCLC. Furthermore, the effects of transfection-induced upregulation of miR-361-5p on the NSCLC cell line H23 were assessed. Overexpression of miR-361-5p inhibited the proliferation and colony formation ability of H23 cells. In addition, apoptosis of H23 cells was induced by upregulation of miR-361-5p. Furthermore, signal transducer and activator of transcription 6 (STAT6) was confirmed as a direct target of miR-361-5p by a dual-luciferase reporter assay. Moreover, inhibition of STAT6 by small interfering RNA or miR-361-5p also decreased the expression of B-cell lymphoma extra large (Bcl-xL). In vivo, miR-361-5p significantly reduced tumor growth in a nude mouse xenograft model, and suppressed STAT6 and Bcl-xL expression. In conclusion, the present study indicated that miR-361-5p may represent a novel molecular tool for therapeutic and diagnostic strategies in NSCLC.
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spelling pubmed-46261612016-02-23 MicroRNA-361-5p suppresses cancer progression by targeting signal transducer and activator of transcription 6 in non-small cell lung cancer MA, YUEFENG BAO, CHUANEN KONG, RANRAN XING, XIN ZHANG, YAYA LI, SHAOMIN ZHANG, WEI JIANG, JIANTAO ZHANG, JIN QIAO, ZHE ZHANG, DANJIE MA, ZHENCHUAN SUN, LIANGZHANG ZHOU, BIN Mol Med Rep Articles The incidence of non-small cell lung cancer (NSCLC) has significantly increased in China, while the prognosis of affected patients is poor. The pathogenesis of NSCLC is thought to be regulated by microRNAs (miRs). The present study used a miR array in order to determine the expression of miR-361-5p, which was significantly lower in NSCLC tissues compared with that in adjacent tissues, indicating a crucial role of miR-361-5p during the progression of NSCLC. Furthermore, the effects of transfection-induced upregulation of miR-361-5p on the NSCLC cell line H23 were assessed. Overexpression of miR-361-5p inhibited the proliferation and colony formation ability of H23 cells. In addition, apoptosis of H23 cells was induced by upregulation of miR-361-5p. Furthermore, signal transducer and activator of transcription 6 (STAT6) was confirmed as a direct target of miR-361-5p by a dual-luciferase reporter assay. Moreover, inhibition of STAT6 by small interfering RNA or miR-361-5p also decreased the expression of B-cell lymphoma extra large (Bcl-xL). In vivo, miR-361-5p significantly reduced tumor growth in a nude mouse xenograft model, and suppressed STAT6 and Bcl-xL expression. In conclusion, the present study indicated that miR-361-5p may represent a novel molecular tool for therapeutic and diagnostic strategies in NSCLC. D.A. Spandidos 2015-11 2015-10-01 /pmc/articles/PMC4626161/ /pubmed/26461141 http://dx.doi.org/10.3892/mmr.2015.4411 Text en Copyright: © Ma 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
MA, YUEFENG
BAO, CHUANEN
KONG, RANRAN
XING, XIN
ZHANG, YAYA
LI, SHAOMIN
ZHANG, WEI
JIANG, JIANTAO
ZHANG, JIN
QIAO, ZHE
ZHANG, DANJIE
MA, ZHENCHUAN
SUN, LIANGZHANG
ZHOU, BIN
MicroRNA-361-5p suppresses cancer progression by targeting signal transducer and activator of transcription 6 in non-small cell lung cancer
title MicroRNA-361-5p suppresses cancer progression by targeting signal transducer and activator of transcription 6 in non-small cell lung cancer
title_full MicroRNA-361-5p suppresses cancer progression by targeting signal transducer and activator of transcription 6 in non-small cell lung cancer
title_fullStr MicroRNA-361-5p suppresses cancer progression by targeting signal transducer and activator of transcription 6 in non-small cell lung cancer
title_full_unstemmed MicroRNA-361-5p suppresses cancer progression by targeting signal transducer and activator of transcription 6 in non-small cell lung cancer
title_short MicroRNA-361-5p suppresses cancer progression by targeting signal transducer and activator of transcription 6 in non-small cell lung cancer
title_sort microrna-361-5p suppresses cancer progression by targeting signal transducer and activator of transcription 6 in non-small cell lung cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626161/
https://www.ncbi.nlm.nih.gov/pubmed/26461141
http://dx.doi.org/10.3892/mmr.2015.4411
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