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Metformin disrupts malignant behavior of oral squamous cell carcinoma via a novel signaling involving Late SV40 factor/Aurora-A
Conventional therapeutic processes in patient with OSCC are associated with several unfavorable effects leading to patients with poor survival rate. Metformin has been shown to protect against a variety of specific diseases, including cancer. However, the precise roles and mechanisms underlying the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430965/ https://www.ncbi.nlm.nih.gov/pubmed/28465536 http://dx.doi.org/10.1038/s41598-017-01353-8 |
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author | Chen, Chang-Han Tsai, Hsin-Ting Chuang, Hui-Ching Shiu, Li-Yen Su, Li-Jen Chiu, Tai-Jan Luo, Sheng-Dean Fang, Fu-Min Huang, Chao-Cheng Chien, Chih-Yen |
author_facet | Chen, Chang-Han Tsai, Hsin-Ting Chuang, Hui-Ching Shiu, Li-Yen Su, Li-Jen Chiu, Tai-Jan Luo, Sheng-Dean Fang, Fu-Min Huang, Chao-Cheng Chien, Chih-Yen |
author_sort | Chen, Chang-Han |
collection | PubMed |
description | Conventional therapeutic processes in patient with OSCC are associated with several unfavorable effects leading to patients with poor survival rate. Metformin has been shown to protect against a variety of specific diseases, including cancer. However, the precise roles and mechanisms underlying the therapeutic effects of metformin on OSCC remain elusive. In the current study, in vitro and xenograft model experiments revealed that metformin inhibited growth and metastasis of oral cancer cells. Importantly, metformin-restrained tumorigenesis of oral cancer was accompanied with strong decrease of both Aurora-A and Late SV40 Factor (LSF) expressions. Furthermore, LSF contributed to Aurora-A-elicited malignancy behaviors of oral cancer via binding to the promoter region of Aurora-A. A significant correlation was observed between LSF and Aurora-A levels in a cohort of specimens of oral cancer. These findings showed that a novel LSF/Aurora-A-signaling inhibition supports the rationale of using metformin as potential OSCC therapeutics. |
format | Online Article Text |
id | pubmed-5430965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54309652017-05-16 Metformin disrupts malignant behavior of oral squamous cell carcinoma via a novel signaling involving Late SV40 factor/Aurora-A Chen, Chang-Han Tsai, Hsin-Ting Chuang, Hui-Ching Shiu, Li-Yen Su, Li-Jen Chiu, Tai-Jan Luo, Sheng-Dean Fang, Fu-Min Huang, Chao-Cheng Chien, Chih-Yen Sci Rep Article Conventional therapeutic processes in patient with OSCC are associated with several unfavorable effects leading to patients with poor survival rate. Metformin has been shown to protect against a variety of specific diseases, including cancer. However, the precise roles and mechanisms underlying the therapeutic effects of metformin on OSCC remain elusive. In the current study, in vitro and xenograft model experiments revealed that metformin inhibited growth and metastasis of oral cancer cells. Importantly, metformin-restrained tumorigenesis of oral cancer was accompanied with strong decrease of both Aurora-A and Late SV40 Factor (LSF) expressions. Furthermore, LSF contributed to Aurora-A-elicited malignancy behaviors of oral cancer via binding to the promoter region of Aurora-A. A significant correlation was observed between LSF and Aurora-A levels in a cohort of specimens of oral cancer. These findings showed that a novel LSF/Aurora-A-signaling inhibition supports the rationale of using metformin as potential OSCC therapeutics. Nature Publishing Group UK 2017-05-02 /pmc/articles/PMC5430965/ /pubmed/28465536 http://dx.doi.org/10.1038/s41598-017-01353-8 Text en © The Author(s) 2017 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 Chen, Chang-Han Tsai, Hsin-Ting Chuang, Hui-Ching Shiu, Li-Yen Su, Li-Jen Chiu, Tai-Jan Luo, Sheng-Dean Fang, Fu-Min Huang, Chao-Cheng Chien, Chih-Yen Metformin disrupts malignant behavior of oral squamous cell carcinoma via a novel signaling involving Late SV40 factor/Aurora-A |
title | Metformin disrupts malignant behavior of oral squamous cell carcinoma via a novel signaling involving Late SV40 factor/Aurora-A |
title_full | Metformin disrupts malignant behavior of oral squamous cell carcinoma via a novel signaling involving Late SV40 factor/Aurora-A |
title_fullStr | Metformin disrupts malignant behavior of oral squamous cell carcinoma via a novel signaling involving Late SV40 factor/Aurora-A |
title_full_unstemmed | Metformin disrupts malignant behavior of oral squamous cell carcinoma via a novel signaling involving Late SV40 factor/Aurora-A |
title_short | Metformin disrupts malignant behavior of oral squamous cell carcinoma via a novel signaling involving Late SV40 factor/Aurora-A |
title_sort | metformin disrupts malignant behavior of oral squamous cell carcinoma via a novel signaling involving late sv40 factor/aurora-a |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430965/ https://www.ncbi.nlm.nih.gov/pubmed/28465536 http://dx.doi.org/10.1038/s41598-017-01353-8 |
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