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miR-582-5P induces colorectal cancer cell proliferation by targeting adenomatous polyposis coli
BACKGROUND: microRNA (miRNAs) dysregulation is widely involved in cancer progression and contributed to sustained cell proliferation by directly targeting multiple targets. Therefore, better understand the underlying mechanism of miRNA in carcinogenesis may improve diagnostic and therapeutic strateg...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011851/ https://www.ncbi.nlm.nih.gov/pubmed/27595705 http://dx.doi.org/10.1186/s12957-016-0984-4 |
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author | Shu, Zhenbo Chen, Libo Ding, Dayong |
author_facet | Shu, Zhenbo Chen, Libo Ding, Dayong |
author_sort | Shu, Zhenbo |
collection | PubMed |
description | BACKGROUND: microRNA (miRNAs) dysregulation is widely involved in cancer progression and contributed to sustained cell proliferation by directly targeting multiple targets. Therefore, better understand the underlying mechanism of miRNA in carcinogenesis may improve diagnostic and therapeutic strategies for malignancy. METHODS: We assessed microRNA-582 (miR-582-5P) expression in colorectal cancer (CRC) specimens and cell lines by real-time PCR. Luciferase reporter assay was used to confirm the target associations. Colony formation assay and anchorage-independent growth assay were used to analyze the effect of miR-582-5P on cell proliferation. Adenomatous polyposis coli (APC) gene and protein expression were examined using real-time PCR and western blotting, respectively. RESULTS: miR-582-5P was upregulated in the CRC specimens and cell lines and targeted the 3′ untranslated region of APC directly. miR-582-5P overexpression increased cyclin D1 and c-MYC expression, which subsequently induced CRC cell proliferation in an APC-dependent manner. CONCLUSIONS: Our findings suggest that miR-582-5P plays an important role in the progression of CRC by inducing proliferation and may identify new targets for anti-cancer treatment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12957-016-0984-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5011851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50118512016-09-07 miR-582-5P induces colorectal cancer cell proliferation by targeting adenomatous polyposis coli Shu, Zhenbo Chen, Libo Ding, Dayong World J Surg Oncol Research BACKGROUND: microRNA (miRNAs) dysregulation is widely involved in cancer progression and contributed to sustained cell proliferation by directly targeting multiple targets. Therefore, better understand the underlying mechanism of miRNA in carcinogenesis may improve diagnostic and therapeutic strategies for malignancy. METHODS: We assessed microRNA-582 (miR-582-5P) expression in colorectal cancer (CRC) specimens and cell lines by real-time PCR. Luciferase reporter assay was used to confirm the target associations. Colony formation assay and anchorage-independent growth assay were used to analyze the effect of miR-582-5P on cell proliferation. Adenomatous polyposis coli (APC) gene and protein expression were examined using real-time PCR and western blotting, respectively. RESULTS: miR-582-5P was upregulated in the CRC specimens and cell lines and targeted the 3′ untranslated region of APC directly. miR-582-5P overexpression increased cyclin D1 and c-MYC expression, which subsequently induced CRC cell proliferation in an APC-dependent manner. CONCLUSIONS: Our findings suggest that miR-582-5P plays an important role in the progression of CRC by inducing proliferation and may identify new targets for anti-cancer treatment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12957-016-0984-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-09-06 /pmc/articles/PMC5011851/ /pubmed/27595705 http://dx.doi.org/10.1186/s12957-016-0984-4 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Shu, Zhenbo Chen, Libo Ding, Dayong miR-582-5P induces colorectal cancer cell proliferation by targeting adenomatous polyposis coli |
title | miR-582-5P induces colorectal cancer cell proliferation by targeting adenomatous polyposis coli |
title_full | miR-582-5P induces colorectal cancer cell proliferation by targeting adenomatous polyposis coli |
title_fullStr | miR-582-5P induces colorectal cancer cell proliferation by targeting adenomatous polyposis coli |
title_full_unstemmed | miR-582-5P induces colorectal cancer cell proliferation by targeting adenomatous polyposis coli |
title_short | miR-582-5P induces colorectal cancer cell proliferation by targeting adenomatous polyposis coli |
title_sort | mir-582-5p induces colorectal cancer cell proliferation by targeting adenomatous polyposis coli |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011851/ https://www.ncbi.nlm.nih.gov/pubmed/27595705 http://dx.doi.org/10.1186/s12957-016-0984-4 |
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