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ADAM9 Mediates Triple-Negative Breast Cancer Progression via AKT/NF-κB Pathway
Upregulation of a disintegrin and metalloprotease 9 (ADAM9) is correlated with progression of cancers, such as prostate, bladder, and pancreatic cancers. However, its role in triple-negative breast cancer (TNBC) is still unclear. Our study aimed to investigate whether ADAM9 is upregulated and promot...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317048/ https://www.ncbi.nlm.nih.gov/pubmed/32637415 http://dx.doi.org/10.3389/fmed.2020.00214 |
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author | Zhou, Rui Cho, William C. S. Ma, Victor Cheuk, Wah So, Yik-Ka Wong, S. C. Cesar Zhang, Mingrong Li, Cong Sun, Yujie Zhang, Hong Chan, Lawrence W. C. Tian, Mei |
author_facet | Zhou, Rui Cho, William C. S. Ma, Victor Cheuk, Wah So, Yik-Ka Wong, S. C. Cesar Zhang, Mingrong Li, Cong Sun, Yujie Zhang, Hong Chan, Lawrence W. C. Tian, Mei |
author_sort | Zhou, Rui |
collection | PubMed |
description | Upregulation of a disintegrin and metalloprotease 9 (ADAM9) is correlated with progression of cancers, such as prostate, bladder, and pancreatic cancers. However, its role in triple-negative breast cancer (TNBC) is still unclear. Our study aimed to investigate whether ADAM9 is upregulated and promoted the aggressiveness in TNBC. Breast cancer cell lines and patient specimens were used to evaluate the ADAM9 expression by western blotting and immunohistochemistry staining, respectively. Compared with the non-TNBC, ADAM9 expression was significantly increased in TNBC cells and TNBC patient specimens. Based on the data acquired from public databases, the correlation between ADAM9 expression and breast cancer patient survival was analyzed by Kaplan-Meier method. It was shown that ADAM9 overexpression was significantly correlated with poorer survival in patients with TNBC. Furthermore, ADAM9 in TNBC cells was knocked down by small interference RNA and then studied by the MTT/colony formation assay, wound healing assay and transwell invasion assay on the cell proliferation, migration, and invasion, respectively. We found that inhibiting ADAM9 expression suppressed TNBC cell proliferation, migration, and invasion by lowering the activation of AKT/NF-κB pathway. Our results demonstrated that ADAM9 is an important molecule in mediating TNBC aggressiveness and may be a potential useful therapeutic target in TNBC treatment. |
format | Online Article Text |
id | pubmed-7317048 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73170482020-07-06 ADAM9 Mediates Triple-Negative Breast Cancer Progression via AKT/NF-κB Pathway Zhou, Rui Cho, William C. S. Ma, Victor Cheuk, Wah So, Yik-Ka Wong, S. C. Cesar Zhang, Mingrong Li, Cong Sun, Yujie Zhang, Hong Chan, Lawrence W. C. Tian, Mei Front Med (Lausanne) Medicine Upregulation of a disintegrin and metalloprotease 9 (ADAM9) is correlated with progression of cancers, such as prostate, bladder, and pancreatic cancers. However, its role in triple-negative breast cancer (TNBC) is still unclear. Our study aimed to investigate whether ADAM9 is upregulated and promoted the aggressiveness in TNBC. Breast cancer cell lines and patient specimens were used to evaluate the ADAM9 expression by western blotting and immunohistochemistry staining, respectively. Compared with the non-TNBC, ADAM9 expression was significantly increased in TNBC cells and TNBC patient specimens. Based on the data acquired from public databases, the correlation between ADAM9 expression and breast cancer patient survival was analyzed by Kaplan-Meier method. It was shown that ADAM9 overexpression was significantly correlated with poorer survival in patients with TNBC. Furthermore, ADAM9 in TNBC cells was knocked down by small interference RNA and then studied by the MTT/colony formation assay, wound healing assay and transwell invasion assay on the cell proliferation, migration, and invasion, respectively. We found that inhibiting ADAM9 expression suppressed TNBC cell proliferation, migration, and invasion by lowering the activation of AKT/NF-κB pathway. Our results demonstrated that ADAM9 is an important molecule in mediating TNBC aggressiveness and may be a potential useful therapeutic target in TNBC treatment. Frontiers Media S.A. 2020-06-19 /pmc/articles/PMC7317048/ /pubmed/32637415 http://dx.doi.org/10.3389/fmed.2020.00214 Text en Copyright © 2020 Zhou, Cho, Ma, Cheuk, So, Wong, Zhang, Li, Sun, Zhang, Chan and Tian. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Zhou, Rui Cho, William C. S. Ma, Victor Cheuk, Wah So, Yik-Ka Wong, S. C. Cesar Zhang, Mingrong Li, Cong Sun, Yujie Zhang, Hong Chan, Lawrence W. C. Tian, Mei ADAM9 Mediates Triple-Negative Breast Cancer Progression via AKT/NF-κB Pathway |
title | ADAM9 Mediates Triple-Negative Breast Cancer Progression via AKT/NF-κB Pathway |
title_full | ADAM9 Mediates Triple-Negative Breast Cancer Progression via AKT/NF-κB Pathway |
title_fullStr | ADAM9 Mediates Triple-Negative Breast Cancer Progression via AKT/NF-κB Pathway |
title_full_unstemmed | ADAM9 Mediates Triple-Negative Breast Cancer Progression via AKT/NF-κB Pathway |
title_short | ADAM9 Mediates Triple-Negative Breast Cancer Progression via AKT/NF-κB Pathway |
title_sort | adam9 mediates triple-negative breast cancer progression via akt/nf-κb pathway |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317048/ https://www.ncbi.nlm.nih.gov/pubmed/32637415 http://dx.doi.org/10.3389/fmed.2020.00214 |
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