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Carbon Ion Irradiation Enhances the Anti-tumor Efficiency in Tongue Squamous Cell Carcinoma via Modulating the FAK Signaling

Oral cancer is a very aggressive disease with high rates of recurrence and metastasis. This study aimed at addressing how efficiently tongue cancer is suppressed after carbon ion irradiation. Here, the close relationship between upregulated expression of focal adhesion kinase (FAK) and high metastat...

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Autores principales: Si, Qingzong, Ye, Qian, Bing, Zhitong, Fan, Ruihong, Hu, Xiaoli, Liu, Bin, Wang, Jizeng, Liu, Yang, An, Xiaoli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7901966/
https://www.ncbi.nlm.nih.gov/pubmed/33634070
http://dx.doi.org/10.3389/fpubh.2021.631118
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author Si, Qingzong
Ye, Qian
Bing, Zhitong
Fan, Ruihong
Hu, Xiaoli
Liu, Bin
Wang, Jizeng
Liu, Yang
An, Xiaoli
author_facet Si, Qingzong
Ye, Qian
Bing, Zhitong
Fan, Ruihong
Hu, Xiaoli
Liu, Bin
Wang, Jizeng
Liu, Yang
An, Xiaoli
author_sort Si, Qingzong
collection PubMed
description Oral cancer is a very aggressive disease with high rates of recurrence and metastasis. This study aimed at addressing how efficiently tongue cancer is suppressed after carbon ion irradiation. Here, the close relationship between upregulated expression of focal adhesion kinase (FAK) and high metastatic status in tongue squamous cell carcinoma patients was validated using bioinformatics and immunohistochemical analyses. Our data indicated that FAK suppression significantly enhanced the killing effect induced by irradiation in the tongue cancer cell line CAL27, as evidenced by increased apoptotic induction and reduced colony formation. More importantly, in FAK-deficient cells, carbon ion irradiation was shown to remarkably inhibit migration and invasion by delaying wound healing and slowing down motility. Further studies revealed that irradiation exposure caused disorganization of the actin cytoskeleton and reduced cell adhesive energy in FAK-deficient cells. Moreover, carbon ion treatment, in combination with FAK silencing, markedly blocked the phosphorylation levels of FAK, and paxillin, which partly contributed to the reduced motility of tongue squamous cell carcinoma CAL27 cells. Collectively, these results suggest that the prominent obstructing role of carbon ion irradiation in the growth inhibition and metastatic behavior of tumors, including attenuation of cell adhesiveness, motility, and invasiveness, could be distinctly modulated by FAK-mediated downstream pathways.
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spelling pubmed-79019662021-02-24 Carbon Ion Irradiation Enhances the Anti-tumor Efficiency in Tongue Squamous Cell Carcinoma via Modulating the FAK Signaling Si, Qingzong Ye, Qian Bing, Zhitong Fan, Ruihong Hu, Xiaoli Liu, Bin Wang, Jizeng Liu, Yang An, Xiaoli Front Public Health Public Health Oral cancer is a very aggressive disease with high rates of recurrence and metastasis. This study aimed at addressing how efficiently tongue cancer is suppressed after carbon ion irradiation. Here, the close relationship between upregulated expression of focal adhesion kinase (FAK) and high metastatic status in tongue squamous cell carcinoma patients was validated using bioinformatics and immunohistochemical analyses. Our data indicated that FAK suppression significantly enhanced the killing effect induced by irradiation in the tongue cancer cell line CAL27, as evidenced by increased apoptotic induction and reduced colony formation. More importantly, in FAK-deficient cells, carbon ion irradiation was shown to remarkably inhibit migration and invasion by delaying wound healing and slowing down motility. Further studies revealed that irradiation exposure caused disorganization of the actin cytoskeleton and reduced cell adhesive energy in FAK-deficient cells. Moreover, carbon ion treatment, in combination with FAK silencing, markedly blocked the phosphorylation levels of FAK, and paxillin, which partly contributed to the reduced motility of tongue squamous cell carcinoma CAL27 cells. Collectively, these results suggest that the prominent obstructing role of carbon ion irradiation in the growth inhibition and metastatic behavior of tumors, including attenuation of cell adhesiveness, motility, and invasiveness, could be distinctly modulated by FAK-mediated downstream pathways. Frontiers Media S.A. 2021-02-03 /pmc/articles/PMC7901966/ /pubmed/33634070 http://dx.doi.org/10.3389/fpubh.2021.631118 Text en Copyright © 2021 Si, Ye, Bing, Fan, Hu, Liu, Wang, Liu and An. 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 Public Health
Si, Qingzong
Ye, Qian
Bing, Zhitong
Fan, Ruihong
Hu, Xiaoli
Liu, Bin
Wang, Jizeng
Liu, Yang
An, Xiaoli
Carbon Ion Irradiation Enhances the Anti-tumor Efficiency in Tongue Squamous Cell Carcinoma via Modulating the FAK Signaling
title Carbon Ion Irradiation Enhances the Anti-tumor Efficiency in Tongue Squamous Cell Carcinoma via Modulating the FAK Signaling
title_full Carbon Ion Irradiation Enhances the Anti-tumor Efficiency in Tongue Squamous Cell Carcinoma via Modulating the FAK Signaling
title_fullStr Carbon Ion Irradiation Enhances the Anti-tumor Efficiency in Tongue Squamous Cell Carcinoma via Modulating the FAK Signaling
title_full_unstemmed Carbon Ion Irradiation Enhances the Anti-tumor Efficiency in Tongue Squamous Cell Carcinoma via Modulating the FAK Signaling
title_short Carbon Ion Irradiation Enhances the Anti-tumor Efficiency in Tongue Squamous Cell Carcinoma via Modulating the FAK Signaling
title_sort carbon ion irradiation enhances the anti-tumor efficiency in tongue squamous cell carcinoma via modulating the fak signaling
topic Public Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7901966/
https://www.ncbi.nlm.nih.gov/pubmed/33634070
http://dx.doi.org/10.3389/fpubh.2021.631118
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