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The Clinical Significance of the Expression of FEN1 in Primary Osteosarcoma

PURPOSE: The aim of this research was to investigate the clinical significance of the expression of flap structure-specific endonuclease 1 (FEN1) in primary osteosarcoma. METHODS: The expression of FEN1 was detected by immunohistochemistry analysis. The association of the expression of FEN1 in osteo...

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Autores principales: Zhong, Guangxian, Wang, Yunqing, Wei, Hongxiang, Chen, Meifang, Lin, Huangfeng, Huang, Zhen, Huang, Jinlong, Wang, Shenglin, Lin, Jianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8504935/
https://www.ncbi.nlm.nih.gov/pubmed/34675615
http://dx.doi.org/10.2147/IJGM.S335817
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author Zhong, Guangxian
Wang, Yunqing
Wei, Hongxiang
Chen, Meifang
Lin, Huangfeng
Huang, Zhen
Huang, Jinlong
Wang, Shenglin
Lin, Jianhua
author_facet Zhong, Guangxian
Wang, Yunqing
Wei, Hongxiang
Chen, Meifang
Lin, Huangfeng
Huang, Zhen
Huang, Jinlong
Wang, Shenglin
Lin, Jianhua
author_sort Zhong, Guangxian
collection PubMed
description PURPOSE: The aim of this research was to investigate the clinical significance of the expression of flap structure-specific endonuclease 1 (FEN1) in primary osteosarcoma. METHODS: The expression of FEN1 was detected by immunohistochemistry analysis. The association of the expression of FEN1 in osteosarcoma with clinicopathological parameters was analyzed by using χ(2) test or Fisher’s exact test. Survival analyses were performed by Kaplan–Meier method and Cox proportional hazards regression model. RESULTS: Of the 40 osteosarcoma patients, 19 (47.5%) patients presented with FEN1 high expression, while in the non-neoplastic bone specimens, the FEN1 high expression was observed in 10% (3/30), the positive expression rate in osteosarcoma patients was significantly higher than that of non-neoplastic bone specimens (P< 0.01). Univariate analysis indicated that the progression-free survival (PFS) and overall survival (OS) were correlated with the expression level of FEN1 (PFS, P < 0.001; OS, P = 0.002), Enneking staging (PFS, P = 0.026; OS, P = 0.044) and chemotherapy response (PFS, P = 0.019; OS, P = 0.031). Multivariate analysis demonstrated that FEN1 expression was an independent prognostic factor for the PFS (HR = 4.73, P = 0.002) and OS (HR = 4.01, P = 0.038) of osteosarcoma patients. CONCLUSION: This study showed that FEN1 was overexpressed in osteosarcoma patients and positively associated with poor prognosis of osteosarcoma patients. Further studies should focus on the relative mechanisms and the targeted FEN1 therapies for osteosarcoma.
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spelling pubmed-85049352021-10-20 The Clinical Significance of the Expression of FEN1 in Primary Osteosarcoma Zhong, Guangxian Wang, Yunqing Wei, Hongxiang Chen, Meifang Lin, Huangfeng Huang, Zhen Huang, Jinlong Wang, Shenglin Lin, Jianhua Int J Gen Med Original Research PURPOSE: The aim of this research was to investigate the clinical significance of the expression of flap structure-specific endonuclease 1 (FEN1) in primary osteosarcoma. METHODS: The expression of FEN1 was detected by immunohistochemistry analysis. The association of the expression of FEN1 in osteosarcoma with clinicopathological parameters was analyzed by using χ(2) test or Fisher’s exact test. Survival analyses were performed by Kaplan–Meier method and Cox proportional hazards regression model. RESULTS: Of the 40 osteosarcoma patients, 19 (47.5%) patients presented with FEN1 high expression, while in the non-neoplastic bone specimens, the FEN1 high expression was observed in 10% (3/30), the positive expression rate in osteosarcoma patients was significantly higher than that of non-neoplastic bone specimens (P< 0.01). Univariate analysis indicated that the progression-free survival (PFS) and overall survival (OS) were correlated with the expression level of FEN1 (PFS, P < 0.001; OS, P = 0.002), Enneking staging (PFS, P = 0.026; OS, P = 0.044) and chemotherapy response (PFS, P = 0.019; OS, P = 0.031). Multivariate analysis demonstrated that FEN1 expression was an independent prognostic factor for the PFS (HR = 4.73, P = 0.002) and OS (HR = 4.01, P = 0.038) of osteosarcoma patients. CONCLUSION: This study showed that FEN1 was overexpressed in osteosarcoma patients and positively associated with poor prognosis of osteosarcoma patients. Further studies should focus on the relative mechanisms and the targeted FEN1 therapies for osteosarcoma. Dove 2021-10-07 /pmc/articles/PMC8504935/ /pubmed/34675615 http://dx.doi.org/10.2147/IJGM.S335817 Text en © 2021 Zhong et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Zhong, Guangxian
Wang, Yunqing
Wei, Hongxiang
Chen, Meifang
Lin, Huangfeng
Huang, Zhen
Huang, Jinlong
Wang, Shenglin
Lin, Jianhua
The Clinical Significance of the Expression of FEN1 in Primary Osteosarcoma
title The Clinical Significance of the Expression of FEN1 in Primary Osteosarcoma
title_full The Clinical Significance of the Expression of FEN1 in Primary Osteosarcoma
title_fullStr The Clinical Significance of the Expression of FEN1 in Primary Osteosarcoma
title_full_unstemmed The Clinical Significance of the Expression of FEN1 in Primary Osteosarcoma
title_short The Clinical Significance of the Expression of FEN1 in Primary Osteosarcoma
title_sort clinical significance of the expression of fen1 in primary osteosarcoma
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8504935/
https://www.ncbi.nlm.nih.gov/pubmed/34675615
http://dx.doi.org/10.2147/IJGM.S335817
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