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Impact of RhoA overexpression on clinical outcomes in cervical squamous cell carcinoma treated with concurrent chemoradiotherapy

The Rho-associated coiled-coil-containing protein kinase (ROCK) pathway is known to influence metastasis in several cancers; however, the impact of the pathway on clinical outcomes in patients undergoing radiotherapy remains unknown. In the present study, the expression of RhoA, RhoC, ROCK-1, ROCK-2...

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Autores principales: Tanaka, Keiichi, Matsumoto, Yoshitaka, Ishikawa, Hitoshi, Fukumitsu, Nobuyoshi, Numajiri, Haruko, Murofushi, Keiko, Oshiro, Yoshiko, Okumura, Toshiyuki, Satoh, Toyomi, Sakurai, Hideyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7246076/
https://www.ncbi.nlm.nih.gov/pubmed/31976530
http://dx.doi.org/10.1093/jrr/rrz093
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author Tanaka, Keiichi
Matsumoto, Yoshitaka
Ishikawa, Hitoshi
Fukumitsu, Nobuyoshi
Numajiri, Haruko
Murofushi, Keiko
Oshiro, Yoshiko
Okumura, Toshiyuki
Satoh, Toyomi
Sakurai, Hideyuki
author_facet Tanaka, Keiichi
Matsumoto, Yoshitaka
Ishikawa, Hitoshi
Fukumitsu, Nobuyoshi
Numajiri, Haruko
Murofushi, Keiko
Oshiro, Yoshiko
Okumura, Toshiyuki
Satoh, Toyomi
Sakurai, Hideyuki
author_sort Tanaka, Keiichi
collection PubMed
description The Rho-associated coiled-coil-containing protein kinase (ROCK) pathway is known to influence metastasis in several cancers; however, the impact of the pathway on clinical outcomes in patients undergoing radiotherapy remains unknown. In the present study, the expression of RhoA, RhoC, ROCK-1, ROCK-2 and p53 was immunohistochemically evaluated using biopsy specimens obtained from 49 patients with stage II–III cervical squamous cell carcinoma treated with concurrent chemoradiotherapy (CCRT). The relationship between the expression of these proteins and patient outcomes was investigated. RhoA overexpression was associated with significantly impaired disease-free survival and distant metastasis-free survival (P = 0.045 and P = 0.041, respectively) in stage III cancer patients. No differences in survival were observed based on the expression of the other proteins among stage III cancer patients. In stage II cancer patients, no differences in survival were noted based on the expression of any of the proteins. The expression of RhoA was able to successfully differentiate cervical cancer patients with distant metastasis after CCRT. This information may help stratify patients according to the risk of metastasis, thereby leading to the potential to provide individualized treatment.
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spelling pubmed-72460762020-05-28 Impact of RhoA overexpression on clinical outcomes in cervical squamous cell carcinoma treated with concurrent chemoradiotherapy Tanaka, Keiichi Matsumoto, Yoshitaka Ishikawa, Hitoshi Fukumitsu, Nobuyoshi Numajiri, Haruko Murofushi, Keiko Oshiro, Yoshiko Okumura, Toshiyuki Satoh, Toyomi Sakurai, Hideyuki J Radiat Res Regular Paper The Rho-associated coiled-coil-containing protein kinase (ROCK) pathway is known to influence metastasis in several cancers; however, the impact of the pathway on clinical outcomes in patients undergoing radiotherapy remains unknown. In the present study, the expression of RhoA, RhoC, ROCK-1, ROCK-2 and p53 was immunohistochemically evaluated using biopsy specimens obtained from 49 patients with stage II–III cervical squamous cell carcinoma treated with concurrent chemoradiotherapy (CCRT). The relationship between the expression of these proteins and patient outcomes was investigated. RhoA overexpression was associated with significantly impaired disease-free survival and distant metastasis-free survival (P = 0.045 and P = 0.041, respectively) in stage III cancer patients. No differences in survival were observed based on the expression of the other proteins among stage III cancer patients. In stage II cancer patients, no differences in survival were noted based on the expression of any of the proteins. The expression of RhoA was able to successfully differentiate cervical cancer patients with distant metastasis after CCRT. This information may help stratify patients according to the risk of metastasis, thereby leading to the potential to provide individualized treatment. Oxford University Press 2020-01-24 /pmc/articles/PMC7246076/ /pubmed/31976530 http://dx.doi.org/10.1093/jrr/rrz093 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of The Japanese Radiation Research Society and Japanese Society for Radiation Oncology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Regular Paper
Tanaka, Keiichi
Matsumoto, Yoshitaka
Ishikawa, Hitoshi
Fukumitsu, Nobuyoshi
Numajiri, Haruko
Murofushi, Keiko
Oshiro, Yoshiko
Okumura, Toshiyuki
Satoh, Toyomi
Sakurai, Hideyuki
Impact of RhoA overexpression on clinical outcomes in cervical squamous cell carcinoma treated with concurrent chemoradiotherapy
title Impact of RhoA overexpression on clinical outcomes in cervical squamous cell carcinoma treated with concurrent chemoradiotherapy
title_full Impact of RhoA overexpression on clinical outcomes in cervical squamous cell carcinoma treated with concurrent chemoradiotherapy
title_fullStr Impact of RhoA overexpression on clinical outcomes in cervical squamous cell carcinoma treated with concurrent chemoradiotherapy
title_full_unstemmed Impact of RhoA overexpression on clinical outcomes in cervical squamous cell carcinoma treated with concurrent chemoradiotherapy
title_short Impact of RhoA overexpression on clinical outcomes in cervical squamous cell carcinoma treated with concurrent chemoradiotherapy
title_sort impact of rhoa overexpression on clinical outcomes in cervical squamous cell carcinoma treated with concurrent chemoradiotherapy
topic Regular Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7246076/
https://www.ncbi.nlm.nih.gov/pubmed/31976530
http://dx.doi.org/10.1093/jrr/rrz093
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