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MiR-183/-96/-182 cluster is up-regulated in most breast cancers and increases cell proliferation and migration

INTRODUCTION: The miR-183/-96/-182 cluster is a conserved polycistronic microRNA (miRNA) cluster which is highly expressed in most breast cancers. Although there are some sporadic reports which demonstrate the importance of each miRNA in this cluster in breast cancer, the biological roles of this cl...

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Autores principales: Li, Pei, Sheng, Cheng, Huang, Lingling, Zhang, Hui, Huang, Lihua, Cheng, Zeneng, Zhu, Qubo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303194/
https://www.ncbi.nlm.nih.gov/pubmed/25394902
http://dx.doi.org/10.1186/s13058-014-0473-z
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author Li, Pei
Sheng, Cheng
Huang, Lingling
Zhang, Hui
Huang, Lihua
Cheng, Zeneng
Zhu, Qubo
author_facet Li, Pei
Sheng, Cheng
Huang, Lingling
Zhang, Hui
Huang, Lihua
Cheng, Zeneng
Zhu, Qubo
author_sort Li, Pei
collection PubMed
description INTRODUCTION: The miR-183/-96/-182 cluster is a conserved polycistronic microRNA (miRNA) cluster which is highly expressed in most breast cancers. Although there are some sporadic reports which demonstrate the importance of each miRNA in this cluster in breast cancer, the biological roles of this cluster as a whole and its regulation mechanisms in breast cancer are still unclear. We compared the expression of this cluster in different cancer types, analyzed the regulation mechanism of this cluster, identified new target genes, and examined the impact of this cluster on breast cancer cells. METHODS: The miRNA level was detected by LNA-based northern blot and Real-time PCR, and was also analyzed from TCGA dataset. Bioinformatics research and luciferase assay were applied to find the promoter regions and transcription factors. To investigate the biological effects of the miR-183/-96 /-182 cluster in breast cancer, we generated miR-96, miR-182 and miR-183 overexpression stable cell lines to check the overdose effects; we also used miR-Down™ antagomir for each miRNA as well as miR-183/-96 /-182 cluster sponge lentivirus to check the knockdown effects. Growth, migration, cell cycle profile and survival of these cells was then monitored by colony formation assay, MTT assay, cell wound healing assay, flow cytometry and microscopy. The target gene was validated by Real-time PCR, luciferase assay, Western blot and Phalloidin/DAPI counterstaining. RESULTS: The miR-183/-96/-182 cluster was highly expressed in most breast cancers, and its transcription is disordered in breast cancer. The miR-183/-96/-182 cluster was transcribed in the same pri-miRNA and its transcription was regulated by ZEB1 and HSF2. It increased breast cell growth by promoting more rapid completion of mitosis, promoted cell migration and was essential for cell survival. MiR-183 targeted the RAB21 mRNA directly in breast cancer. CONCLUSION: The miR-183/-96/-182 cluster is up-regulated in most breast cancer. It functions as an oncogene in breast cancer as it increases cell proliferation and migration. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13058-014-0473-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-43031942015-01-23 MiR-183/-96/-182 cluster is up-regulated in most breast cancers and increases cell proliferation and migration Li, Pei Sheng, Cheng Huang, Lingling Zhang, Hui Huang, Lihua Cheng, Zeneng Zhu, Qubo Breast Cancer Res Research Article INTRODUCTION: The miR-183/-96/-182 cluster is a conserved polycistronic microRNA (miRNA) cluster which is highly expressed in most breast cancers. Although there are some sporadic reports which demonstrate the importance of each miRNA in this cluster in breast cancer, the biological roles of this cluster as a whole and its regulation mechanisms in breast cancer are still unclear. We compared the expression of this cluster in different cancer types, analyzed the regulation mechanism of this cluster, identified new target genes, and examined the impact of this cluster on breast cancer cells. METHODS: The miRNA level was detected by LNA-based northern blot and Real-time PCR, and was also analyzed from TCGA dataset. Bioinformatics research and luciferase assay were applied to find the promoter regions and transcription factors. To investigate the biological effects of the miR-183/-96 /-182 cluster in breast cancer, we generated miR-96, miR-182 and miR-183 overexpression stable cell lines to check the overdose effects; we also used miR-Down™ antagomir for each miRNA as well as miR-183/-96 /-182 cluster sponge lentivirus to check the knockdown effects. Growth, migration, cell cycle profile and survival of these cells was then monitored by colony formation assay, MTT assay, cell wound healing assay, flow cytometry and microscopy. The target gene was validated by Real-time PCR, luciferase assay, Western blot and Phalloidin/DAPI counterstaining. RESULTS: The miR-183/-96/-182 cluster was highly expressed in most breast cancers, and its transcription is disordered in breast cancer. The miR-183/-96/-182 cluster was transcribed in the same pri-miRNA and its transcription was regulated by ZEB1 and HSF2. It increased breast cell growth by promoting more rapid completion of mitosis, promoted cell migration and was essential for cell survival. MiR-183 targeted the RAB21 mRNA directly in breast cancer. CONCLUSION: The miR-183/-96/-182 cluster is up-regulated in most breast cancer. It functions as an oncogene in breast cancer as it increases cell proliferation and migration. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13058-014-0473-z) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-14 2014 /pmc/articles/PMC4303194/ /pubmed/25394902 http://dx.doi.org/10.1186/s13058-014-0473-z Text en © Li et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Article
Li, Pei
Sheng, Cheng
Huang, Lingling
Zhang, Hui
Huang, Lihua
Cheng, Zeneng
Zhu, Qubo
MiR-183/-96/-182 cluster is up-regulated in most breast cancers and increases cell proliferation and migration
title MiR-183/-96/-182 cluster is up-regulated in most breast cancers and increases cell proliferation and migration
title_full MiR-183/-96/-182 cluster is up-regulated in most breast cancers and increases cell proliferation and migration
title_fullStr MiR-183/-96/-182 cluster is up-regulated in most breast cancers and increases cell proliferation and migration
title_full_unstemmed MiR-183/-96/-182 cluster is up-regulated in most breast cancers and increases cell proliferation and migration
title_short MiR-183/-96/-182 cluster is up-regulated in most breast cancers and increases cell proliferation and migration
title_sort mir-183/-96/-182 cluster is up-regulated in most breast cancers and increases cell proliferation and migration
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303194/
https://www.ncbi.nlm.nih.gov/pubmed/25394902
http://dx.doi.org/10.1186/s13058-014-0473-z
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