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FSCN1 is an effective marker of poor prognosis and a potential therapeutic target in human tongue squamous cell carcinoma

To estimate the value of FSCN1 in evaluating the prognosis and guiding the targeted therapy for patients with tongue squamous cell carcinoma (TSCC). Using the Oncomine database, we found some genes especially FSCN1 differentially expressed between TSCC samples and tongue normal samples. So we compar...

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Autores principales: Chen, Yue, Tian, Tian, Li, Zhi-Yong, Wang, Chun-Yang, Deng, Rong, Deng, Wei-Ye, Yang, An-kui, Chen, Yan-Feng, Li, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6494834/
https://www.ncbi.nlm.nih.gov/pubmed/31043585
http://dx.doi.org/10.1038/s41419-019-1574-5
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author Chen, Yue
Tian, Tian
Li, Zhi-Yong
Wang, Chun-Yang
Deng, Rong
Deng, Wei-Ye
Yang, An-kui
Chen, Yan-Feng
Li, Hao
author_facet Chen, Yue
Tian, Tian
Li, Zhi-Yong
Wang, Chun-Yang
Deng, Rong
Deng, Wei-Ye
Yang, An-kui
Chen, Yan-Feng
Li, Hao
author_sort Chen, Yue
collection PubMed
description To estimate the value of FSCN1 in evaluating the prognosis and guiding the targeted therapy for patients with tongue squamous cell carcinoma (TSCC). Using the Oncomine database, we found some genes especially FSCN1 differentially expressed between TSCC samples and tongue normal samples. So we compared FSCN1 expression between TSCC and normal cell lines and knocked down FSCN1 in TSCC cells to observe its influence on the viability and trans-migration in vitro and tumor growth in vivo. Then we measured FSCN1 expression in human cancer tissues and adjacent non-carcinoma tissues (ANT) and explored the relationship between FSCN1 expression and clinical pathological factors and prognosis in TSCC patients. We found that FSCN1 is expressed higher in TSCC cells than in normal cells. Knockdown of FSCN1 reduced TSCC cell viability and trans-migration in vitro and impaired tumor growth in vivo. FSCN1 also expressed higher in human TSCC than in ANT. In addition, FSCN1 expression was related to N classification, clinical stage and relapse. TSCC patients with over-expression of FSCN1 had worse prognosis. In conclusion, over-expression of FSCN1 indicates worse prognosis for patients with TSCC and FSCN1 may be a potential prognostic biomarker and therapeutic target in TSCC.
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spelling pubmed-64948342019-05-02 FSCN1 is an effective marker of poor prognosis and a potential therapeutic target in human tongue squamous cell carcinoma Chen, Yue Tian, Tian Li, Zhi-Yong Wang, Chun-Yang Deng, Rong Deng, Wei-Ye Yang, An-kui Chen, Yan-Feng Li, Hao Cell Death Dis Article To estimate the value of FSCN1 in evaluating the prognosis and guiding the targeted therapy for patients with tongue squamous cell carcinoma (TSCC). Using the Oncomine database, we found some genes especially FSCN1 differentially expressed between TSCC samples and tongue normal samples. So we compared FSCN1 expression between TSCC and normal cell lines and knocked down FSCN1 in TSCC cells to observe its influence on the viability and trans-migration in vitro and tumor growth in vivo. Then we measured FSCN1 expression in human cancer tissues and adjacent non-carcinoma tissues (ANT) and explored the relationship between FSCN1 expression and clinical pathological factors and prognosis in TSCC patients. We found that FSCN1 is expressed higher in TSCC cells than in normal cells. Knockdown of FSCN1 reduced TSCC cell viability and trans-migration in vitro and impaired tumor growth in vivo. FSCN1 also expressed higher in human TSCC than in ANT. In addition, FSCN1 expression was related to N classification, clinical stage and relapse. TSCC patients with over-expression of FSCN1 had worse prognosis. In conclusion, over-expression of FSCN1 indicates worse prognosis for patients with TSCC and FSCN1 may be a potential prognostic biomarker and therapeutic target in TSCC. Nature Publishing Group UK 2019-05-01 /pmc/articles/PMC6494834/ /pubmed/31043585 http://dx.doi.org/10.1038/s41419-019-1574-5 Text en © The Author(s) 2019 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, Yue
Tian, Tian
Li, Zhi-Yong
Wang, Chun-Yang
Deng, Rong
Deng, Wei-Ye
Yang, An-kui
Chen, Yan-Feng
Li, Hao
FSCN1 is an effective marker of poor prognosis and a potential therapeutic target in human tongue squamous cell carcinoma
title FSCN1 is an effective marker of poor prognosis and a potential therapeutic target in human tongue squamous cell carcinoma
title_full FSCN1 is an effective marker of poor prognosis and a potential therapeutic target in human tongue squamous cell carcinoma
title_fullStr FSCN1 is an effective marker of poor prognosis and a potential therapeutic target in human tongue squamous cell carcinoma
title_full_unstemmed FSCN1 is an effective marker of poor prognosis and a potential therapeutic target in human tongue squamous cell carcinoma
title_short FSCN1 is an effective marker of poor prognosis and a potential therapeutic target in human tongue squamous cell carcinoma
title_sort fscn1 is an effective marker of poor prognosis and a potential therapeutic target in human tongue squamous cell carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6494834/
https://www.ncbi.nlm.nih.gov/pubmed/31043585
http://dx.doi.org/10.1038/s41419-019-1574-5
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