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miRNA-186-5p inhibits migration, invasion and proliferation of breast cancer cells by targeting SBEM
The paper aimed to investigate the effect of miR186-5p on invasion and migration of breast cancer cells and its molecular mechanism. MicroRNA-186-5p was found to be low expressed in breast cancer and highly expressed in SBEM by bioinformatics analysis. After transfecting MDA-MB-231 cells with miR-18...
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/PMC10415540/ https://www.ncbi.nlm.nih.gov/pubmed/37477531 http://dx.doi.org/10.18632/aging.204887 |
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author | Hao, Hui Wang, Bingsheng Yang, Lin Sang, Yinzhou Xu, Wei Liu, Wei Zhang, Lili Jiang, Da |
author_facet | Hao, Hui Wang, Bingsheng Yang, Lin Sang, Yinzhou Xu, Wei Liu, Wei Zhang, Lili Jiang, Da |
author_sort | Hao, Hui |
collection | PubMed |
description | The paper aimed to investigate the effect of miR186-5p on invasion and migration of breast cancer cells and its molecular mechanism. MicroRNA-186-5p was found to be low expressed in breast cancer and highly expressed in SBEM by bioinformatics analysis. After transfecting MDA-MB-231 cells with miR-186-5p inhibitor NC, miR-186-5p inhibitor, miR-186-5p mimic NC and miR-186-5p mimic, respectively. The migration and invasive ability of breast cancer cells were detected by cell scratch test and Transwell test. Moreover, after adding 740 Y-P to the miR-186-5p mimic NC group and miR-186-5p mimic group cells, SBEM and PI3K pathway-related proteins were detected by Western blotting and proliferation of the cancer cells was evaluated by monoclonal cell experiment. Meanwhile, exogenous miR-186-5p mimic in MDA-MB-231 cells significantly inhibited the expression of SBEM, p-PI3K, p-AKT and their downstream pathways, MMP1, MMP3, MMP9, CyclinD1, PCNA and CyclinB1 proteins and reduced proliferation of breast cancer cells. Furthermore, the expression of SBEM protein in the miR-186-5p mimic + 740Y-P group was significantly lower than the miR-186-5p mimic NC + 740Y-P group after adding 740 Y-P. However, there were no significant changes in the protein’s levels associated with PI3K pathway and the cancer cells proliferation. These results suggest that low expression of miR-186-5p in breast cancer results in an abnormally high expression of SBEM, activation of PI3K/AKT signaling pathway, promoting migration and invasion of human breast cancer cells. |
format | Online Article Text |
id | pubmed-10415540 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-104155402023-08-12 miRNA-186-5p inhibits migration, invasion and proliferation of breast cancer cells by targeting SBEM Hao, Hui Wang, Bingsheng Yang, Lin Sang, Yinzhou Xu, Wei Liu, Wei Zhang, Lili Jiang, Da Aging (Albany NY) Research Paper The paper aimed to investigate the effect of miR186-5p on invasion and migration of breast cancer cells and its molecular mechanism. MicroRNA-186-5p was found to be low expressed in breast cancer and highly expressed in SBEM by bioinformatics analysis. After transfecting MDA-MB-231 cells with miR-186-5p inhibitor NC, miR-186-5p inhibitor, miR-186-5p mimic NC and miR-186-5p mimic, respectively. The migration and invasive ability of breast cancer cells were detected by cell scratch test and Transwell test. Moreover, after adding 740 Y-P to the miR-186-5p mimic NC group and miR-186-5p mimic group cells, SBEM and PI3K pathway-related proteins were detected by Western blotting and proliferation of the cancer cells was evaluated by monoclonal cell experiment. Meanwhile, exogenous miR-186-5p mimic in MDA-MB-231 cells significantly inhibited the expression of SBEM, p-PI3K, p-AKT and their downstream pathways, MMP1, MMP3, MMP9, CyclinD1, PCNA and CyclinB1 proteins and reduced proliferation of breast cancer cells. Furthermore, the expression of SBEM protein in the miR-186-5p mimic + 740Y-P group was significantly lower than the miR-186-5p mimic NC + 740Y-P group after adding 740 Y-P. However, there were no significant changes in the protein’s levels associated with PI3K pathway and the cancer cells proliferation. These results suggest that low expression of miR-186-5p in breast cancer results in an abnormally high expression of SBEM, activation of PI3K/AKT signaling pathway, promoting migration and invasion of human breast cancer cells. Impact Journals 2023-07-20 /pmc/articles/PMC10415540/ /pubmed/37477531 http://dx.doi.org/10.18632/aging.204887 Text en Copyright: © 2023 Hao 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 Hao, Hui Wang, Bingsheng Yang, Lin Sang, Yinzhou Xu, Wei Liu, Wei Zhang, Lili Jiang, Da miRNA-186-5p inhibits migration, invasion and proliferation of breast cancer cells by targeting SBEM |
title | miRNA-186-5p inhibits migration, invasion and proliferation of breast cancer cells by targeting SBEM |
title_full | miRNA-186-5p inhibits migration, invasion and proliferation of breast cancer cells by targeting SBEM |
title_fullStr | miRNA-186-5p inhibits migration, invasion and proliferation of breast cancer cells by targeting SBEM |
title_full_unstemmed | miRNA-186-5p inhibits migration, invasion and proliferation of breast cancer cells by targeting SBEM |
title_short | miRNA-186-5p inhibits migration, invasion and proliferation of breast cancer cells by targeting SBEM |
title_sort | mirna-186-5p inhibits migration, invasion and proliferation of breast cancer cells by targeting sbem |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415540/ https://www.ncbi.nlm.nih.gov/pubmed/37477531 http://dx.doi.org/10.18632/aging.204887 |
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