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Role of TMPRSS4 Modulation in Breast Cancer Cell Proliferation
BACKGROUND: TMPRSS4 is a novel Type II transmembrane serine protease found at the surface of the cells and is involved in the development and cancer progression. However, TMPRSS4 functions in breast cancer remain poor understand. The present study investigated the function of TMPRSS4 in the breast c...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
West Asia Organization for Cancer Prevention
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7021625/ https://www.ncbi.nlm.nih.gov/pubmed/31244309 http://dx.doi.org/10.31557/APJCP.2019.20.6.1849 |
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author | Assani, Ganiou Yessoufou, Akadiri Xiong, Yudi Segbo, Julien Yu, Xiaoyan Zhou, Fuxiang Zhou, Yunfeng |
author_facet | Assani, Ganiou Yessoufou, Akadiri Xiong, Yudi Segbo, Julien Yu, Xiaoyan Zhou, Fuxiang Zhou, Yunfeng |
author_sort | Assani, Ganiou |
collection | PubMed |
description | BACKGROUND: TMPRSS4 is a novel Type II transmembrane serine protease found at the surface of the cells and is involved in the development and cancer progression. However, TMPRSS4 functions in breast cancer remain poor understand. The present study investigated the function of TMPRSS4 in the breast cancer cells and the potential mechanistic action underling. MATERIALS AND METHODS: The lentiviral vectors causing TMPRSS4 down-regulation and over-expression were established and transfected in MDA-MB-468 and MCF-7 cells, respectively. By using the CCK-8 assay, cell proliferation was analyzed. Moreover, western blot was used to detect the expression of certain proteins related to cell apoptosis (Bax and Bcl2) signaling pathway and telomere maintenance (POT1, TPP1, and UBE2D3). Cell cycle and cell apoptosis were also analyzed by using the Flow cytometry analysis. TMPRSS4 expression was detected at the mRNA level and protein level by performing qPCR and western blot technique, respectively. RESULTS: TMPRSS4 expression is inhibited in stable transfected MDA-MB-468-shTMPRSS4 cells compared to the control MDA-MB-468-NC and its expression is up-regulated in stable transfected MCF-7-TMPTSS4 compared to its control MCF-7-NC. Moreover, TMPRSS4 silencing in breast cancer reduces cells proliferation by promoting cell cycle arrest in G2/M phase, cell apoptosis, and telomere maintenance impairment while the TMPRSS4 overexpression increases cells proliferation through cell apoptosis reduction and telomere maintenance reinforcement associated with insignificant change in cell cycle progression. CONCLUSION: TMPRSS4 plays important roles in cancer progression and may be considered as a good therapeutic target for cancer gene therapy especially breast cancer. |
format | Online Article Text |
id | pubmed-7021625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | West Asia Organization for Cancer Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-70216252020-02-25 Role of TMPRSS4 Modulation in Breast Cancer Cell Proliferation Assani, Ganiou Yessoufou, Akadiri Xiong, Yudi Segbo, Julien Yu, Xiaoyan Zhou, Fuxiang Zhou, Yunfeng Asian Pac J Cancer Prev Research Article BACKGROUND: TMPRSS4 is a novel Type II transmembrane serine protease found at the surface of the cells and is involved in the development and cancer progression. However, TMPRSS4 functions in breast cancer remain poor understand. The present study investigated the function of TMPRSS4 in the breast cancer cells and the potential mechanistic action underling. MATERIALS AND METHODS: The lentiviral vectors causing TMPRSS4 down-regulation and over-expression were established and transfected in MDA-MB-468 and MCF-7 cells, respectively. By using the CCK-8 assay, cell proliferation was analyzed. Moreover, western blot was used to detect the expression of certain proteins related to cell apoptosis (Bax and Bcl2) signaling pathway and telomere maintenance (POT1, TPP1, and UBE2D3). Cell cycle and cell apoptosis were also analyzed by using the Flow cytometry analysis. TMPRSS4 expression was detected at the mRNA level and protein level by performing qPCR and western blot technique, respectively. RESULTS: TMPRSS4 expression is inhibited in stable transfected MDA-MB-468-shTMPRSS4 cells compared to the control MDA-MB-468-NC and its expression is up-regulated in stable transfected MCF-7-TMPTSS4 compared to its control MCF-7-NC. Moreover, TMPRSS4 silencing in breast cancer reduces cells proliferation by promoting cell cycle arrest in G2/M phase, cell apoptosis, and telomere maintenance impairment while the TMPRSS4 overexpression increases cells proliferation through cell apoptosis reduction and telomere maintenance reinforcement associated with insignificant change in cell cycle progression. CONCLUSION: TMPRSS4 plays important roles in cancer progression and may be considered as a good therapeutic target for cancer gene therapy especially breast cancer. West Asia Organization for Cancer Prevention 2019 /pmc/articles/PMC7021625/ /pubmed/31244309 http://dx.doi.org/10.31557/APJCP.2019.20.6.1849 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Assani, Ganiou Yessoufou, Akadiri Xiong, Yudi Segbo, Julien Yu, Xiaoyan Zhou, Fuxiang Zhou, Yunfeng Role of TMPRSS4 Modulation in Breast Cancer Cell Proliferation |
title | Role of TMPRSS4 Modulation in Breast Cancer Cell Proliferation |
title_full | Role of TMPRSS4 Modulation in Breast Cancer Cell Proliferation |
title_fullStr | Role of TMPRSS4 Modulation in Breast Cancer Cell Proliferation |
title_full_unstemmed | Role of TMPRSS4 Modulation in Breast Cancer Cell Proliferation |
title_short | Role of TMPRSS4 Modulation in Breast Cancer Cell Proliferation |
title_sort | role of tmprss4 modulation in breast cancer cell proliferation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7021625/ https://www.ncbi.nlm.nih.gov/pubmed/31244309 http://dx.doi.org/10.31557/APJCP.2019.20.6.1849 |
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