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Aurora-A affects radiosenstivity in cervical squamous cell carcinoma and predicts poor prognosis

BACKGROUND: Definitive radiation therapy (RT) (with or without cisplatin-based chemotherapy) is one of the most effective treatments for cervical squamous cell carcinoma (CSCC), but efficacy is limited due to resistance. In the present study, we investigated the relationship between the expression o...

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Autores principales: Ma, Yuhua, Yang, Jie, Wang, Ruozheng, Zhang, Zegao, Qi, Xiaoli, Liu, Chunhua, Ma, Miaomiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458225/
https://www.ncbi.nlm.nih.gov/pubmed/28404933
http://dx.doi.org/10.18632/oncotarget.15663
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author Ma, Yuhua
Yang, Jie
Wang, Ruozheng
Zhang, Zegao
Qi, Xiaoli
Liu, Chunhua
Ma, Miaomiao
author_facet Ma, Yuhua
Yang, Jie
Wang, Ruozheng
Zhang, Zegao
Qi, Xiaoli
Liu, Chunhua
Ma, Miaomiao
author_sort Ma, Yuhua
collection PubMed
description BACKGROUND: Definitive radiation therapy (RT) (with or without cisplatin-based chemotherapy) is one of the most effective treatments for cervical squamous cell carcinoma (CSCC), but efficacy is limited due to resistance. In the present study, we investigated the relationship between the expression of Aurora kinase A (Aurora-A, AURKA)and response to RT in patients with CSCC. METHODS: The expression of Aurora-A in biopsy specimens of untreated primary tumors in 129 Uyghur patients with CSCC was investigated immunohistochemically. Primary treatment in these patients was definitive radical RT, which consisted of pelvic RT plus brachytherapy (total point A dose:70–85 Gy) (with or without cisplatin-based chemotherapy). The prognostic value of tumoral Aurora-A expression and patients’ clinical outcomes were evaluated. RESULTS: Aurora-A expression was significantly associated with lymph node metastasis (P<0.001), large tumor size (P<0.001), low hemoglobin (Hb) level (P=0.011) and recurrence (P<0.001), but not other clinicopathological factors. Definitive RT was unfavorable in patients with high Aurora-A expression (P < 0.001). In 129 enrolled patients, lymph node metastasis, large tumor size, low Hb level, and AURKA overexpression were prognostic factors for both recurrent free survival (RFS) and overall survival (OS) in univariate analysis. However, only high AURKA expression was an adverse independent risk factor for both RFS (hazard ratio, 3.953; 95% CI, 1.473-10.638; P = 0.006) and OS (hazard ratio 9.091; 95%CI 2.597-32.258; P<0.001) in multivariate analyses. CONCLUSIONS: Aurora-A may serve as a predictive biomarker of radiation response and a therapeutic target to reverse radiation therapy resistance.
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spelling pubmed-54582252017-06-08 Aurora-A affects radiosenstivity in cervical squamous cell carcinoma and predicts poor prognosis Ma, Yuhua Yang, Jie Wang, Ruozheng Zhang, Zegao Qi, Xiaoli Liu, Chunhua Ma, Miaomiao Oncotarget Research Paper BACKGROUND: Definitive radiation therapy (RT) (with or without cisplatin-based chemotherapy) is one of the most effective treatments for cervical squamous cell carcinoma (CSCC), but efficacy is limited due to resistance. In the present study, we investigated the relationship between the expression of Aurora kinase A (Aurora-A, AURKA)and response to RT in patients with CSCC. METHODS: The expression of Aurora-A in biopsy specimens of untreated primary tumors in 129 Uyghur patients with CSCC was investigated immunohistochemically. Primary treatment in these patients was definitive radical RT, which consisted of pelvic RT plus brachytherapy (total point A dose:70–85 Gy) (with or without cisplatin-based chemotherapy). The prognostic value of tumoral Aurora-A expression and patients’ clinical outcomes were evaluated. RESULTS: Aurora-A expression was significantly associated with lymph node metastasis (P<0.001), large tumor size (P<0.001), low hemoglobin (Hb) level (P=0.011) and recurrence (P<0.001), but not other clinicopathological factors. Definitive RT was unfavorable in patients with high Aurora-A expression (P < 0.001). In 129 enrolled patients, lymph node metastasis, large tumor size, low Hb level, and AURKA overexpression were prognostic factors for both recurrent free survival (RFS) and overall survival (OS) in univariate analysis. However, only high AURKA expression was an adverse independent risk factor for both RFS (hazard ratio, 3.953; 95% CI, 1.473-10.638; P = 0.006) and OS (hazard ratio 9.091; 95%CI 2.597-32.258; P<0.001) in multivariate analyses. CONCLUSIONS: Aurora-A may serve as a predictive biomarker of radiation response and a therapeutic target to reverse radiation therapy resistance. Impact Journals LLC 2017-02-24 /pmc/articles/PMC5458225/ /pubmed/28404933 http://dx.doi.org/10.18632/oncotarget.15663 Text en Copyright: © 2017 Ma et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Ma, Yuhua
Yang, Jie
Wang, Ruozheng
Zhang, Zegao
Qi, Xiaoli
Liu, Chunhua
Ma, Miaomiao
Aurora-A affects radiosenstivity in cervical squamous cell carcinoma and predicts poor prognosis
title Aurora-A affects radiosenstivity in cervical squamous cell carcinoma and predicts poor prognosis
title_full Aurora-A affects radiosenstivity in cervical squamous cell carcinoma and predicts poor prognosis
title_fullStr Aurora-A affects radiosenstivity in cervical squamous cell carcinoma and predicts poor prognosis
title_full_unstemmed Aurora-A affects radiosenstivity in cervical squamous cell carcinoma and predicts poor prognosis
title_short Aurora-A affects radiosenstivity in cervical squamous cell carcinoma and predicts poor prognosis
title_sort aurora-a affects radiosenstivity in cervical squamous cell carcinoma and predicts poor prognosis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458225/
https://www.ncbi.nlm.nih.gov/pubmed/28404933
http://dx.doi.org/10.18632/oncotarget.15663
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