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miR-500 promotes cell proliferation by directly targetting LRP1B in prostate cancer

Accumulating evidence suggests that miRNAs play a crucial role in the development of prostate cancer (PC); however, the role of miR-500 in PC remains poorly understood. The data presented here reveal abnormal increases in miR-500 expression in PC tissues and cell lines. Suppression of miR-500 expres...

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Detalles Bibliográficos
Autores principales: Zhang, Zhaoli, Cui, Ran, Li, Hui, Li, Jinlong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449515/
https://www.ncbi.nlm.nih.gov/pubmed/30877185
http://dx.doi.org/10.1042/BSR20181854
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author Zhang, Zhaoli
Cui, Ran
Li, Hui
Li, Jinlong
author_facet Zhang, Zhaoli
Cui, Ran
Li, Hui
Li, Jinlong
author_sort Zhang, Zhaoli
collection PubMed
description Accumulating evidence suggests that miRNAs play a crucial role in the development of prostate cancer (PC); however, the role of miR-500 in PC remains poorly understood. The data presented here reveal abnormal increases in miR-500 expression in PC tissues and cell lines. Suppression of miR-500 expression significantly inhibited the proliferation of PC-3 and LnCap cells and was negatively regulative with low-density lipoprotein receptor-related protein 1B (LRP1B). Increased cell cycle arrest at the G1 stage and decreased protein expression of cyclinD1 and CDK2 was observed in response to miR-500 knockdown in PC-3 and LnCap cells, in combination with LRP1B overexpression. LRP1B was identified as a target of miR-500 and was significantly decreased in PC tissues. Taken together, these findings demonstrate that miR-500 plays an important role in the proliferation of PC cells via the inhibition of LRP1B expression.
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spelling pubmed-64495152019-04-17 miR-500 promotes cell proliferation by directly targetting LRP1B in prostate cancer Zhang, Zhaoli Cui, Ran Li, Hui Li, Jinlong Biosci Rep Research Articles Accumulating evidence suggests that miRNAs play a crucial role in the development of prostate cancer (PC); however, the role of miR-500 in PC remains poorly understood. The data presented here reveal abnormal increases in miR-500 expression in PC tissues and cell lines. Suppression of miR-500 expression significantly inhibited the proliferation of PC-3 and LnCap cells and was negatively regulative with low-density lipoprotein receptor-related protein 1B (LRP1B). Increased cell cycle arrest at the G1 stage and decreased protein expression of cyclinD1 and CDK2 was observed in response to miR-500 knockdown in PC-3 and LnCap cells, in combination with LRP1B overexpression. LRP1B was identified as a target of miR-500 and was significantly decreased in PC tissues. Taken together, these findings demonstrate that miR-500 plays an important role in the proliferation of PC cells via the inhibition of LRP1B expression. Portland Press Ltd. 2019-04-05 /pmc/articles/PMC6449515/ /pubmed/30877185 http://dx.doi.org/10.1042/BSR20181854 Text en © 2019 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Articles
Zhang, Zhaoli
Cui, Ran
Li, Hui
Li, Jinlong
miR-500 promotes cell proliferation by directly targetting LRP1B in prostate cancer
title miR-500 promotes cell proliferation by directly targetting LRP1B in prostate cancer
title_full miR-500 promotes cell proliferation by directly targetting LRP1B in prostate cancer
title_fullStr miR-500 promotes cell proliferation by directly targetting LRP1B in prostate cancer
title_full_unstemmed miR-500 promotes cell proliferation by directly targetting LRP1B in prostate cancer
title_short miR-500 promotes cell proliferation by directly targetting LRP1B in prostate cancer
title_sort mir-500 promotes cell proliferation by directly targetting lrp1b in prostate cancer
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449515/
https://www.ncbi.nlm.nih.gov/pubmed/30877185
http://dx.doi.org/10.1042/BSR20181854
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