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MicroRNA-488 inhibits proliferation and motility of tumor cells via downregulating FSCN1, modulated by Notch3 in breast carcinomas

As important modulators in multiple physiological processes, microRNAs (miRNAs) have been reported in various malignant tumors, including breast cancer. The current study investigated the function of a new tumor suppressor microRNA, miR-488, and its molecular mechanism of metastasis in breast cancer...

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Autores principales: Wu, Yang, Yuan, Ming-Heng, Wu, Hua-Tao, Chen, Wen-Jia, Zhang, Man-Li, Ye, Qian-Qian, Liu, Jing, Zhang, Guo-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7585581/
https://www.ncbi.nlm.nih.gov/pubmed/33099573
http://dx.doi.org/10.1038/s41419-020-03121-5
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author Wu, Yang
Yuan, Ming-Heng
Wu, Hua-Tao
Chen, Wen-Jia
Zhang, Man-Li
Ye, Qian-Qian
Liu, Jing
Zhang, Guo-Jun
author_facet Wu, Yang
Yuan, Ming-Heng
Wu, Hua-Tao
Chen, Wen-Jia
Zhang, Man-Li
Ye, Qian-Qian
Liu, Jing
Zhang, Guo-Jun
author_sort Wu, Yang
collection PubMed
description As important modulators in multiple physiological processes, microRNAs (miRNAs) have been reported in various malignant tumors, including breast cancer. The current study investigated the function of a new tumor suppressor microRNA, miR-488, and its molecular mechanism of metastasis in breast cancers. CCK8 and transwell assays revealed that the upregulated miR-488 level significantly inhibited the proliferation and migration of breast cancer cells. As a potential downstream gene, the mRNA and protein level of FSCN1 was suppressed by increased miR-488 and vice versa. Luciferase assay showed that miR-488 directly bind to the 3′UTR of FSCN1 and suppressed the translation process of FSCN1. The promoter region of miR-488 was directly bound by Notch3 and promoted the expression of miR-488 transcriptionally. Immunohistochemistry results revealed that in patients with breast cancer, the expression of Notch3 and were negatively correlated with the FSCN1 levels significantly. Therefore, the current finding predicted miR-488 as a tumor suppressor molecule in breast cancer, and demonstrated that Notch3/miR-488/FSCN1 axis is established and involved in regulating the metastasis of breast cancers, providing novel therapeutic targets for patients with breast cancers.
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spelling pubmed-75855812020-10-26 MicroRNA-488 inhibits proliferation and motility of tumor cells via downregulating FSCN1, modulated by Notch3 in breast carcinomas Wu, Yang Yuan, Ming-Heng Wu, Hua-Tao Chen, Wen-Jia Zhang, Man-Li Ye, Qian-Qian Liu, Jing Zhang, Guo-Jun Cell Death Dis Article As important modulators in multiple physiological processes, microRNAs (miRNAs) have been reported in various malignant tumors, including breast cancer. The current study investigated the function of a new tumor suppressor microRNA, miR-488, and its molecular mechanism of metastasis in breast cancers. CCK8 and transwell assays revealed that the upregulated miR-488 level significantly inhibited the proliferation and migration of breast cancer cells. As a potential downstream gene, the mRNA and protein level of FSCN1 was suppressed by increased miR-488 and vice versa. Luciferase assay showed that miR-488 directly bind to the 3′UTR of FSCN1 and suppressed the translation process of FSCN1. The promoter region of miR-488 was directly bound by Notch3 and promoted the expression of miR-488 transcriptionally. Immunohistochemistry results revealed that in patients with breast cancer, the expression of Notch3 and were negatively correlated with the FSCN1 levels significantly. Therefore, the current finding predicted miR-488 as a tumor suppressor molecule in breast cancer, and demonstrated that Notch3/miR-488/FSCN1 axis is established and involved in regulating the metastasis of breast cancers, providing novel therapeutic targets for patients with breast cancers. Nature Publishing Group UK 2020-10-24 /pmc/articles/PMC7585581/ /pubmed/33099573 http://dx.doi.org/10.1038/s41419-020-03121-5 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wu, Yang
Yuan, Ming-Heng
Wu, Hua-Tao
Chen, Wen-Jia
Zhang, Man-Li
Ye, Qian-Qian
Liu, Jing
Zhang, Guo-Jun
MicroRNA-488 inhibits proliferation and motility of tumor cells via downregulating FSCN1, modulated by Notch3 in breast carcinomas
title MicroRNA-488 inhibits proliferation and motility of tumor cells via downregulating FSCN1, modulated by Notch3 in breast carcinomas
title_full MicroRNA-488 inhibits proliferation and motility of tumor cells via downregulating FSCN1, modulated by Notch3 in breast carcinomas
title_fullStr MicroRNA-488 inhibits proliferation and motility of tumor cells via downregulating FSCN1, modulated by Notch3 in breast carcinomas
title_full_unstemmed MicroRNA-488 inhibits proliferation and motility of tumor cells via downregulating FSCN1, modulated by Notch3 in breast carcinomas
title_short MicroRNA-488 inhibits proliferation and motility of tumor cells via downregulating FSCN1, modulated by Notch3 in breast carcinomas
title_sort microrna-488 inhibits proliferation and motility of tumor cells via downregulating fscn1, modulated by notch3 in breast carcinomas
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7585581/
https://www.ncbi.nlm.nih.gov/pubmed/33099573
http://dx.doi.org/10.1038/s41419-020-03121-5
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