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The oncogenic miR-429 promotes triple-negative breast cancer progression by degrading DLC1
Lines of evidence have demonstrated that the oncogenic miRNAs are pivotal to the progression of breast cancer. In this study, we investigated the biological traits of microRNA-429 (miR-429) in triple-negative breast cancer (TNBC) and the underlying molecular mechanism. We found that miR-429 was nota...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10564445/ https://www.ncbi.nlm.nih.gov/pubmed/37737712 http://dx.doi.org/10.18632/aging.205051 |
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author | Li, Yao Meng, Xue Luo, Yuqing Luo, Shuai Li, Jin Zeng, Jiafei Huang, Xiang Wang, Jinjing |
author_facet | Li, Yao Meng, Xue Luo, Yuqing Luo, Shuai Li, Jin Zeng, Jiafei Huang, Xiang Wang, Jinjing |
author_sort | Li, Yao |
collection | PubMed |
description | Lines of evidence have demonstrated that the oncogenic miRNAs are pivotal to the progression of breast cancer. In this study, we investigated the biological traits of microRNA-429 (miR-429) in triple-negative breast cancer (TNBC) and the underlying molecular mechanism. We found that miR-429 was notably overexpressed in TNBC, and promoted TNBC cell proliferation, migration, and invasion by degrading the tumor suppressor DLC1. In conclusion, our findings reveal the mechanism of tumorigenic miR-429 in TNBC, which paves the way for target therapies translation in clinical settings. |
format | Online Article Text |
id | pubmed-10564445 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-105644452023-10-11 The oncogenic miR-429 promotes triple-negative breast cancer progression by degrading DLC1 Li, Yao Meng, Xue Luo, Yuqing Luo, Shuai Li, Jin Zeng, Jiafei Huang, Xiang Wang, Jinjing Aging (Albany NY) Research Paper Lines of evidence have demonstrated that the oncogenic miRNAs are pivotal to the progression of breast cancer. In this study, we investigated the biological traits of microRNA-429 (miR-429) in triple-negative breast cancer (TNBC) and the underlying molecular mechanism. We found that miR-429 was notably overexpressed in TNBC, and promoted TNBC cell proliferation, migration, and invasion by degrading the tumor suppressor DLC1. In conclusion, our findings reveal the mechanism of tumorigenic miR-429 in TNBC, which paves the way for target therapies translation in clinical settings. Impact Journals 2023-09-21 /pmc/articles/PMC10564445/ /pubmed/37737712 http://dx.doi.org/10.18632/aging.205051 Text en Copyright: © 2023 Li et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Li, Yao Meng, Xue Luo, Yuqing Luo, Shuai Li, Jin Zeng, Jiafei Huang, Xiang Wang, Jinjing The oncogenic miR-429 promotes triple-negative breast cancer progression by degrading DLC1 |
title | The oncogenic miR-429 promotes triple-negative breast cancer progression by degrading DLC1 |
title_full | The oncogenic miR-429 promotes triple-negative breast cancer progression by degrading DLC1 |
title_fullStr | The oncogenic miR-429 promotes triple-negative breast cancer progression by degrading DLC1 |
title_full_unstemmed | The oncogenic miR-429 promotes triple-negative breast cancer progression by degrading DLC1 |
title_short | The oncogenic miR-429 promotes triple-negative breast cancer progression by degrading DLC1 |
title_sort | oncogenic mir-429 promotes triple-negative breast cancer progression by degrading dlc1 |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10564445/ https://www.ncbi.nlm.nih.gov/pubmed/37737712 http://dx.doi.org/10.18632/aging.205051 |
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