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MicroRNA-610 inhibits tumor growth of melanoma by targeting LRP6

Accumulating evidence showed that aberrant miRNAs expression was involved in initiation and progression of melanoma. However, the investigation of different miRNAs in melanoma remain attractive. In this research, we demonstrated that miR-610 expression was decreased in melanoma tissues and cell line...

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Detalles Bibliográficos
Autores principales: Zhang, Guangjing, Ai, Dongfang, Yang, Xiufang, Ji, Shanshan, Wang, Zhengxiang, Feng, Shijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722568/
https://www.ncbi.nlm.nih.gov/pubmed/29228616
http://dx.doi.org/10.18632/oncotarget.22125
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author Zhang, Guangjing
Ai, Dongfang
Yang, Xiufang
Ji, Shanshan
Wang, Zhengxiang
Feng, Shijun
author_facet Zhang, Guangjing
Ai, Dongfang
Yang, Xiufang
Ji, Shanshan
Wang, Zhengxiang
Feng, Shijun
author_sort Zhang, Guangjing
collection PubMed
description Accumulating evidence showed that aberrant miRNAs expression was involved in initiation and progression of melanoma. However, the investigation of different miRNAs in melanoma remain attractive. In this research, we demonstrated that miR-610 expression was decreased in melanoma tissues and cell lines. The clinical data showed that the reduced miR-610 expression was obviously associated with adverse prognostic characteristics. Furthermore, our results suggested that miR-610 had a function of prognostic indicator for 5-year predicted-survival of melanoma patients. The ectopic overexpression of miR-610 suppressed cell proliferation, cell cycle progression and promoted apoptosis while miR-610 knockdown reversed the effect in vitro and in vivo. Additionally, miR-610 could modulate LRP6 by directly interacting to its 3’-UTR. In clinical samples of melanoma, miR-610 inversely correlated with LRP6. The biological function of miR-610 on melanoma cells was abrogated by alternation of LRP6 expression. In summary, our research indexed that miR-610 had a function of tumor suppressor in regulating the proliferation, cell cycle and apoptosis of melanoma via targeting LRP6. Hence, it may represent a novel potential therapeutic target and prognostic marker for melanoma.
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spelling pubmed-57225682017-12-10 MicroRNA-610 inhibits tumor growth of melanoma by targeting LRP6 Zhang, Guangjing Ai, Dongfang Yang, Xiufang Ji, Shanshan Wang, Zhengxiang Feng, Shijun Oncotarget Research Paper Accumulating evidence showed that aberrant miRNAs expression was involved in initiation and progression of melanoma. However, the investigation of different miRNAs in melanoma remain attractive. In this research, we demonstrated that miR-610 expression was decreased in melanoma tissues and cell lines. The clinical data showed that the reduced miR-610 expression was obviously associated with adverse prognostic characteristics. Furthermore, our results suggested that miR-610 had a function of prognostic indicator for 5-year predicted-survival of melanoma patients. The ectopic overexpression of miR-610 suppressed cell proliferation, cell cycle progression and promoted apoptosis while miR-610 knockdown reversed the effect in vitro and in vivo. Additionally, miR-610 could modulate LRP6 by directly interacting to its 3’-UTR. In clinical samples of melanoma, miR-610 inversely correlated with LRP6. The biological function of miR-610 on melanoma cells was abrogated by alternation of LRP6 expression. In summary, our research indexed that miR-610 had a function of tumor suppressor in regulating the proliferation, cell cycle and apoptosis of melanoma via targeting LRP6. Hence, it may represent a novel potential therapeutic target and prognostic marker for melanoma. Impact Journals LLC 2017-10-26 /pmc/articles/PMC5722568/ /pubmed/29228616 http://dx.doi.org/10.18632/oncotarget.22125 Text en Copyright: © 2017 Zhang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Zhang, Guangjing
Ai, Dongfang
Yang, Xiufang
Ji, Shanshan
Wang, Zhengxiang
Feng, Shijun
MicroRNA-610 inhibits tumor growth of melanoma by targeting LRP6
title MicroRNA-610 inhibits tumor growth of melanoma by targeting LRP6
title_full MicroRNA-610 inhibits tumor growth of melanoma by targeting LRP6
title_fullStr MicroRNA-610 inhibits tumor growth of melanoma by targeting LRP6
title_full_unstemmed MicroRNA-610 inhibits tumor growth of melanoma by targeting LRP6
title_short MicroRNA-610 inhibits tumor growth of melanoma by targeting LRP6
title_sort microrna-610 inhibits tumor growth of melanoma by targeting lrp6
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722568/
https://www.ncbi.nlm.nih.gov/pubmed/29228616
http://dx.doi.org/10.18632/oncotarget.22125
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