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miR-135b-5p enhances doxorubicin-sensitivity of breast cancer cells through targeting anterior gradient 2

BACKGROUND: The pro-oncogenic anterior gradient 2 (AGR2) is involved in tumor growth and drug resistance of breast cancer. Mechanisms that regulate expression of AGR2 still need to be elucidated. METHODS: In this study, expression levels of AGR2 and miR-135b-5p were analyzed in different breast canc...

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Autores principales: Zhang, Ying, Xia, Fan, Zhang, Fan, Cui, Yingying, Wang, Qingling, Liu, Hui, Wu, Yongping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341729/
https://www.ncbi.nlm.nih.gov/pubmed/30665445
http://dx.doi.org/10.1186/s13046-019-1024-3
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author Zhang, Ying
Xia, Fan
Zhang, Fan
Cui, Yingying
Wang, Qingling
Liu, Hui
Wu, Yongping
author_facet Zhang, Ying
Xia, Fan
Zhang, Fan
Cui, Yingying
Wang, Qingling
Liu, Hui
Wu, Yongping
author_sort Zhang, Ying
collection PubMed
description BACKGROUND: The pro-oncogenic anterior gradient 2 (AGR2) is involved in tumor growth and drug resistance of breast cancer. Mechanisms that regulate expression of AGR2 still need to be elucidated. METHODS: In this study, expression levels of AGR2 and miR-135b-5p were analyzed in different breast cancer cell lines as well as in clinical breast cancer tissues. The in vitro and in vivo functional effect of AGR2 and miR-135b-5p were also investigated. A luciferase reporter assay was applied to confirm the interaction between miR-135b-5p and AGR2 mRNA. RESULTS: We identified AGR2 as a target of miR-135b-5p. Expression of AGR2 was up-regulated in doxorubicin-resistant breast cancer cells. AGR2 mediated doxorubicin-sensitivity of breast cancer cells both in vitro and in vivo. miR-135b-5p negatively regulated AGR2-expression of breast cancer cells increasing doxorubicin-sensitivity. However, miR-135b-5p was down-regulated in doxorubicin-resistant breast cancer cells as well as during treatment with doxorubicin, which might be a probable reason for over-expression of AGR2. Up-regulation of miR-135b-5p increased doxorubicin-sensitivity of breast cancer cells in vivo. In addition, levels of AGR2 negatively correlated with levels of miR-135b-5p in clinical breast cancer tissue samples. CONCLUSION: Our results highlight the potential of miR-135b-5p as a target for treating AGR2-expressing breast cancer with doxorubicin-resistance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13046-019-1024-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-63417292019-01-24 miR-135b-5p enhances doxorubicin-sensitivity of breast cancer cells through targeting anterior gradient 2 Zhang, Ying Xia, Fan Zhang, Fan Cui, Yingying Wang, Qingling Liu, Hui Wu, Yongping J Exp Clin Cancer Res Research BACKGROUND: The pro-oncogenic anterior gradient 2 (AGR2) is involved in tumor growth and drug resistance of breast cancer. Mechanisms that regulate expression of AGR2 still need to be elucidated. METHODS: In this study, expression levels of AGR2 and miR-135b-5p were analyzed in different breast cancer cell lines as well as in clinical breast cancer tissues. The in vitro and in vivo functional effect of AGR2 and miR-135b-5p were also investigated. A luciferase reporter assay was applied to confirm the interaction between miR-135b-5p and AGR2 mRNA. RESULTS: We identified AGR2 as a target of miR-135b-5p. Expression of AGR2 was up-regulated in doxorubicin-resistant breast cancer cells. AGR2 mediated doxorubicin-sensitivity of breast cancer cells both in vitro and in vivo. miR-135b-5p negatively regulated AGR2-expression of breast cancer cells increasing doxorubicin-sensitivity. However, miR-135b-5p was down-regulated in doxorubicin-resistant breast cancer cells as well as during treatment with doxorubicin, which might be a probable reason for over-expression of AGR2. Up-regulation of miR-135b-5p increased doxorubicin-sensitivity of breast cancer cells in vivo. In addition, levels of AGR2 negatively correlated with levels of miR-135b-5p in clinical breast cancer tissue samples. CONCLUSION: Our results highlight the potential of miR-135b-5p as a target for treating AGR2-expressing breast cancer with doxorubicin-resistance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13046-019-1024-3) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-21 /pmc/articles/PMC6341729/ /pubmed/30665445 http://dx.doi.org/10.1186/s13046-019-1024-3 Text en © The Author(s). 2019 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
Zhang, Ying
Xia, Fan
Zhang, Fan
Cui, Yingying
Wang, Qingling
Liu, Hui
Wu, Yongping
miR-135b-5p enhances doxorubicin-sensitivity of breast cancer cells through targeting anterior gradient 2
title miR-135b-5p enhances doxorubicin-sensitivity of breast cancer cells through targeting anterior gradient 2
title_full miR-135b-5p enhances doxorubicin-sensitivity of breast cancer cells through targeting anterior gradient 2
title_fullStr miR-135b-5p enhances doxorubicin-sensitivity of breast cancer cells through targeting anterior gradient 2
title_full_unstemmed miR-135b-5p enhances doxorubicin-sensitivity of breast cancer cells through targeting anterior gradient 2
title_short miR-135b-5p enhances doxorubicin-sensitivity of breast cancer cells through targeting anterior gradient 2
title_sort mir-135b-5p enhances doxorubicin-sensitivity of breast cancer cells through targeting anterior gradient 2
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341729/
https://www.ncbi.nlm.nih.gov/pubmed/30665445
http://dx.doi.org/10.1186/s13046-019-1024-3
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