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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Higher Education Press 2016
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.
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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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