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miR-10a inhibits cell proliferation and promotes cell apoptosis by targeting BCL6 in diffuse large B-cell lymphoma
The BCL6 (B-Cell Lymphoma 6) gene is a proto-oncogene that is often expressed in diffuse large B-cell lymphomas (DLBCLs). BCL6 loss of function can kill DLBCL cells, demonstrating that BCL6 is necessary for the survival of DLBCL cells and could be a therapeutic target. In this study, we found that B...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Higher Education Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5205661/ https://www.ncbi.nlm.nih.gov/pubmed/27815824 http://dx.doi.org/10.1007/s13238-016-0316-z |
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author | Fan, Qian Meng, Xiangrui Liang, Hongwei Zhang, Huilai Liu, Xianming Li, Lanfang Li, Wei Sun, Wu Zhang, Haiyang Zen, Ke Zhang, Chen-Yu Zhou, Zhen Chen, Xi Ba, Yi |
author_facet | Fan, Qian Meng, Xiangrui Liang, Hongwei Zhang, Huilai Liu, Xianming Li, Lanfang Li, Wei Sun, Wu Zhang, Haiyang Zen, Ke Zhang, Chen-Yu Zhou, Zhen Chen, Xi Ba, Yi |
author_sort | Fan, Qian |
collection | PubMed |
description | The BCL6 (B-Cell Lymphoma 6) gene is a proto-oncogene that is often expressed in diffuse large B-cell lymphomas (DLBCLs). BCL6 loss of function can kill DLBCL cells, demonstrating that BCL6 is necessary for the survival of DLBCL cells and could be a therapeutic target. In this study, we found that BCL6 protein levels were consistently upregulated in DLBCL tissues, whereas its mRNA levels varied randomly in tissues, suggesting that a post-transcriptional mechanism was involved in BCL6 regulation. We used bioinformatics analysis to search for miRNAs, which potentially target BCL6, and identified specific targeting sites for miR-10a in the 3′-untranslated region (3′-UTR) of BCL6. We further identified an inverse correlation between miR-10a levels and BCL6 protein levels, but not mRNA levels, in DLBCL tumor tissue samples. By overexpressing or knocking down miR-10a in DLBCL cells, we experimentally validated that miR-10a directly recognizes the 3′-UTR of the BCL6 transcript and regulated BCL6 expression. Furthermore, we demonstrated that negatively regulating BCL6 by miR-10a suppressed the proliferation and promoted apoptosis of DLBCL cells. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13238-016-0316-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5205661 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Higher Education Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-52056612017-01-18 miR-10a inhibits cell proliferation and promotes cell apoptosis by targeting BCL6 in diffuse large B-cell lymphoma Fan, Qian Meng, Xiangrui Liang, Hongwei Zhang, Huilai Liu, Xianming Li, Lanfang Li, Wei Sun, Wu Zhang, Haiyang Zen, Ke Zhang, Chen-Yu Zhou, Zhen Chen, Xi Ba, Yi Protein Cell Research Article The BCL6 (B-Cell Lymphoma 6) gene is a proto-oncogene that is often expressed in diffuse large B-cell lymphomas (DLBCLs). BCL6 loss of function can kill DLBCL cells, demonstrating that BCL6 is necessary for the survival of DLBCL cells and could be a therapeutic target. In this study, we found that BCL6 protein levels were consistently upregulated in DLBCL tissues, whereas its mRNA levels varied randomly in tissues, suggesting that a post-transcriptional mechanism was involved in BCL6 regulation. We used bioinformatics analysis to search for miRNAs, which potentially target BCL6, and identified specific targeting sites for miR-10a in the 3′-untranslated region (3′-UTR) of BCL6. We further identified an inverse correlation between miR-10a levels and BCL6 protein levels, but not mRNA levels, in DLBCL tumor tissue samples. By overexpressing or knocking down miR-10a in DLBCL cells, we experimentally validated that miR-10a directly recognizes the 3′-UTR of the BCL6 transcript and regulated BCL6 expression. Furthermore, we demonstrated that negatively regulating BCL6 by miR-10a suppressed the proliferation and promoted apoptosis of DLBCL cells. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13238-016-0316-z) contains supplementary material, which is available to authorized users. Higher Education Press 2016-11-04 2016-12 /pmc/articles/PMC5205661/ /pubmed/27815824 http://dx.doi.org/10.1007/s13238-016-0316-z 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. |
spellingShingle | Research Article Fan, Qian Meng, Xiangrui Liang, Hongwei Zhang, Huilai Liu, Xianming Li, Lanfang Li, Wei Sun, Wu Zhang, Haiyang Zen, Ke Zhang, Chen-Yu Zhou, Zhen Chen, Xi Ba, Yi miR-10a inhibits cell proliferation and promotes cell apoptosis by targeting BCL6 in diffuse large B-cell lymphoma |
title | miR-10a inhibits cell proliferation and promotes cell apoptosis by targeting BCL6 in diffuse large B-cell lymphoma |
title_full | miR-10a inhibits cell proliferation and promotes cell apoptosis by targeting BCL6 in diffuse large B-cell lymphoma |
title_fullStr | miR-10a inhibits cell proliferation and promotes cell apoptosis by targeting BCL6 in diffuse large B-cell lymphoma |
title_full_unstemmed | miR-10a inhibits cell proliferation and promotes cell apoptosis by targeting BCL6 in diffuse large B-cell lymphoma |
title_short | miR-10a inhibits cell proliferation and promotes cell apoptosis by targeting BCL6 in diffuse large B-cell lymphoma |
title_sort | mir-10a inhibits cell proliferation and promotes cell apoptosis by targeting bcl6 in diffuse large b-cell lymphoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5205661/ https://www.ncbi.nlm.nih.gov/pubmed/27815824 http://dx.doi.org/10.1007/s13238-016-0316-z |
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