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microRNA-21 promotes breast cancer proliferation and metastasis by targeting LZTFL1
BACKGROUND: Breast cancer is the most common cancer type in female. As microRNAs play vital role in breast cancer, this study aimed to explore the molecular mechanism and clinical value of miR-21 in breast cancer. METHODS: qRT-PCR was performed to detect miR-21 levels in plasma of 127 healthy contro...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6661096/ https://www.ncbi.nlm.nih.gov/pubmed/31351450 http://dx.doi.org/10.1186/s12885-019-5951-3 |
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author | Wang, Hui Tan, Zheqiong Hu, Hui Liu, Hongzhou Wu, Tangwei Zheng, Chao Wang, Xiuling Luo, Zhenzhao Wang, Jing Liu, Shuiyi Lu, Zhongxin Tu, Jiancheng |
author_facet | Wang, Hui Tan, Zheqiong Hu, Hui Liu, Hongzhou Wu, Tangwei Zheng, Chao Wang, Xiuling Luo, Zhenzhao Wang, Jing Liu, Shuiyi Lu, Zhongxin Tu, Jiancheng |
author_sort | Wang, Hui |
collection | PubMed |
description | BACKGROUND: Breast cancer is the most common cancer type in female. As microRNAs play vital role in breast cancer, this study aimed to explore the molecular mechanism and clinical value of miR-21 in breast cancer. METHODS: qRT-PCR was performed to detect miR-21 levels in plasma of 127 healthy controls, 82 benign breast tumor, 252 breast cancer patients, as well as in breast cancer cell lines. Transwell and wound healing assay were used to analyze breast cancer metastasis in response to miR-21 inhibitor. Colony formation and eFluor™ 670 based flow cytometric analysis were used to test breast cancer proliferation following miR-21 inhibitor treatment. Leucine zipper transcription factor-like 1 (LZTFL1), the target gene of miR-21 was predicted by MIRDB, TargetScan 5.1, PicTar and miRanda. Survival analysis of LZTFL1 levels in breast cancer prognosis was estimated with the Kaplan–Meier method by log-rank test according to data from the Cancer Genome Atlas. Luciferase activity assay was performed to confirm the regulation of miR-21 on LZTFL1. LZTFL1 siRNA and miR-21 inhibitor were co-transfected to breast cancer cells, then cell proliferation, migration and epithelial–mesenchymal transition (EMT) makers were tested. BALB/c nude mice were injected in situ with Hs578T cells stably overexpressing miR-21. Breast tumor growth, metastasis and the expression of EMT markers or LZTFL1 were detected in vivo. RESULTS: Plasma miR-21 levels were elevated in breast cancer patients compared with healthy controls and benign breast tumor patients, and the miR-21 levels were significantly decreased after surgery comparing with pre operation in 44 patients. Inhibition of miR-21 suppressed cell proliferation and metastasis in breast cancer cells. LZTFL1 was identified as a novel target gene of miR-21. Knockdown of LZTFL1 overcame the suppression of miR-21 inhibitor on cell proliferation, metastasis and the expression of EMT markers in breast cancer cells. miR-21 overexpression promoted breast cancer cell proliferation and metastasis in vivo. CONCLUSIONS: These results indicate that plasma miR-21 level is a crucial biomarker for breast cancer diagnosis and targeting miR-21–LZTFL1–EMT axis might be a promising strategy in breast cancer therapy. TRIAL REGISTRATION: Retrospectively registered. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-019-5951-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6661096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-66610962019-08-01 microRNA-21 promotes breast cancer proliferation and metastasis by targeting LZTFL1 Wang, Hui Tan, Zheqiong Hu, Hui Liu, Hongzhou Wu, Tangwei Zheng, Chao Wang, Xiuling Luo, Zhenzhao Wang, Jing Liu, Shuiyi Lu, Zhongxin Tu, Jiancheng BMC Cancer Research Article BACKGROUND: Breast cancer is the most common cancer type in female. As microRNAs play vital role in breast cancer, this study aimed to explore the molecular mechanism and clinical value of miR-21 in breast cancer. METHODS: qRT-PCR was performed to detect miR-21 levels in plasma of 127 healthy controls, 82 benign breast tumor, 252 breast cancer patients, as well as in breast cancer cell lines. Transwell and wound healing assay were used to analyze breast cancer metastasis in response to miR-21 inhibitor. Colony formation and eFluor™ 670 based flow cytometric analysis were used to test breast cancer proliferation following miR-21 inhibitor treatment. Leucine zipper transcription factor-like 1 (LZTFL1), the target gene of miR-21 was predicted by MIRDB, TargetScan 5.1, PicTar and miRanda. Survival analysis of LZTFL1 levels in breast cancer prognosis was estimated with the Kaplan–Meier method by log-rank test according to data from the Cancer Genome Atlas. Luciferase activity assay was performed to confirm the regulation of miR-21 on LZTFL1. LZTFL1 siRNA and miR-21 inhibitor were co-transfected to breast cancer cells, then cell proliferation, migration and epithelial–mesenchymal transition (EMT) makers were tested. BALB/c nude mice were injected in situ with Hs578T cells stably overexpressing miR-21. Breast tumor growth, metastasis and the expression of EMT markers or LZTFL1 were detected in vivo. RESULTS: Plasma miR-21 levels were elevated in breast cancer patients compared with healthy controls and benign breast tumor patients, and the miR-21 levels were significantly decreased after surgery comparing with pre operation in 44 patients. Inhibition of miR-21 suppressed cell proliferation and metastasis in breast cancer cells. LZTFL1 was identified as a novel target gene of miR-21. Knockdown of LZTFL1 overcame the suppression of miR-21 inhibitor on cell proliferation, metastasis and the expression of EMT markers in breast cancer cells. miR-21 overexpression promoted breast cancer cell proliferation and metastasis in vivo. CONCLUSIONS: These results indicate that plasma miR-21 level is a crucial biomarker for breast cancer diagnosis and targeting miR-21–LZTFL1–EMT axis might be a promising strategy in breast cancer therapy. TRIAL REGISTRATION: Retrospectively registered. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-019-5951-3) contains supplementary material, which is available to authorized users. BioMed Central 2019-07-27 /pmc/articles/PMC6661096/ /pubmed/31351450 http://dx.doi.org/10.1186/s12885-019-5951-3 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 Article Wang, Hui Tan, Zheqiong Hu, Hui Liu, Hongzhou Wu, Tangwei Zheng, Chao Wang, Xiuling Luo, Zhenzhao Wang, Jing Liu, Shuiyi Lu, Zhongxin Tu, Jiancheng microRNA-21 promotes breast cancer proliferation and metastasis by targeting LZTFL1 |
title | microRNA-21 promotes breast cancer proliferation and metastasis by targeting LZTFL1 |
title_full | microRNA-21 promotes breast cancer proliferation and metastasis by targeting LZTFL1 |
title_fullStr | microRNA-21 promotes breast cancer proliferation and metastasis by targeting LZTFL1 |
title_full_unstemmed | microRNA-21 promotes breast cancer proliferation and metastasis by targeting LZTFL1 |
title_short | microRNA-21 promotes breast cancer proliferation and metastasis by targeting LZTFL1 |
title_sort | microrna-21 promotes breast cancer proliferation and metastasis by targeting lztfl1 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6661096/ https://www.ncbi.nlm.nih.gov/pubmed/31351450 http://dx.doi.org/10.1186/s12885-019-5951-3 |
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