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Prognostic role of apoptosis-related gene functional variants in advanced non-small-cell lung cancer patients treated with first-line platinum-based chemotherapy

BACKGROUND: Single-nucleotide polymorphisms in apoptosis-related genes have been shown to play a role in the efficacy of platinum-based chemotherapy and may influence clinical outcomes. Our study aimed to evaluate the correlations of four functional single-nucleotide polymorphisms − FAS −670 A>G,...

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Autores principales: Tao, Kai-Yi, Li, Xian-Xing, Xu, Wei-Zhen, Wang, Yin, Zhu, Shuang-Mei, Xie, Hua-Xia, Luo, Wen-Hua, Xu, Yan-Jun, Xu, Xiao-Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298310/
https://www.ncbi.nlm.nih.gov/pubmed/25609982
http://dx.doi.org/10.2147/OTT.S74855
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author Tao, Kai-Yi
Li, Xian-Xing
Xu, Wei-Zhen
Wang, Yin
Zhu, Shuang-Mei
Xie, Hua-Xia
Luo, Wen-Hua
Xu, Yan-Jun
Xu, Xiao-Ling
author_facet Tao, Kai-Yi
Li, Xian-Xing
Xu, Wei-Zhen
Wang, Yin
Zhu, Shuang-Mei
Xie, Hua-Xia
Luo, Wen-Hua
Xu, Yan-Jun
Xu, Xiao-Ling
author_sort Tao, Kai-Yi
collection PubMed
description BACKGROUND: Single-nucleotide polymorphisms in apoptosis-related genes have been shown to play a role in the efficacy of platinum-based chemotherapy and may influence clinical outcomes. Our study aimed to evaluate the correlations of four functional single-nucleotide polymorphisms − FAS −670 A>G, FAS ligand −844 T>C, survivin −31 G>C, and survivin 9386 C>T – with drug response and clinical outcomes in advanced non-small-cell lung cancer patients who received platinum-based chemotherapy. MATERIALS AND METHODS: Polymorphisms were evaluated using the polymerase chain reaction-based restriction fragment-length polymorphism technique. RESULTS: Patients with the CC genotype of FAS −670 A>G had worse overall survival (OS) than those with the CT or TT genotype (P=0.044), with median OS values of 20.1 months, 22.8 months, and 26.0 months, respectively. Furthermore, progression-free survival was associated with the FAS −670 A>G polymorphism (P=0.032). In addition, patients with the TC and CC genotypes of survivin 9386 C>T experienced improved survival compared with patients with the TT genotype (median OS 31.4 months and 22.8 months, respectively). CONCLUSION: The functional FAS −670 A>G and survivin 9386 C>T polymorphisms are potential independent prognostic factors in advanced non-small-cell lung cancer patients treated with platinum-based chemotherapy.
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spelling pubmed-42983102015-01-21 Prognostic role of apoptosis-related gene functional variants in advanced non-small-cell lung cancer patients treated with first-line platinum-based chemotherapy Tao, Kai-Yi Li, Xian-Xing Xu, Wei-Zhen Wang, Yin Zhu, Shuang-Mei Xie, Hua-Xia Luo, Wen-Hua Xu, Yan-Jun Xu, Xiao-Ling Onco Targets Ther Original Research BACKGROUND: Single-nucleotide polymorphisms in apoptosis-related genes have been shown to play a role in the efficacy of platinum-based chemotherapy and may influence clinical outcomes. Our study aimed to evaluate the correlations of four functional single-nucleotide polymorphisms − FAS −670 A>G, FAS ligand −844 T>C, survivin −31 G>C, and survivin 9386 C>T – with drug response and clinical outcomes in advanced non-small-cell lung cancer patients who received platinum-based chemotherapy. MATERIALS AND METHODS: Polymorphisms were evaluated using the polymerase chain reaction-based restriction fragment-length polymorphism technique. RESULTS: Patients with the CC genotype of FAS −670 A>G had worse overall survival (OS) than those with the CT or TT genotype (P=0.044), with median OS values of 20.1 months, 22.8 months, and 26.0 months, respectively. Furthermore, progression-free survival was associated with the FAS −670 A>G polymorphism (P=0.032). In addition, patients with the TC and CC genotypes of survivin 9386 C>T experienced improved survival compared with patients with the TT genotype (median OS 31.4 months and 22.8 months, respectively). CONCLUSION: The functional FAS −670 A>G and survivin 9386 C>T polymorphisms are potential independent prognostic factors in advanced non-small-cell lung cancer patients treated with platinum-based chemotherapy. Dove Medical Press 2015-01-14 /pmc/articles/PMC4298310/ /pubmed/25609982 http://dx.doi.org/10.2147/OTT.S74855 Text en © 2015 Tao et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Tao, Kai-Yi
Li, Xian-Xing
Xu, Wei-Zhen
Wang, Yin
Zhu, Shuang-Mei
Xie, Hua-Xia
Luo, Wen-Hua
Xu, Yan-Jun
Xu, Xiao-Ling
Prognostic role of apoptosis-related gene functional variants in advanced non-small-cell lung cancer patients treated with first-line platinum-based chemotherapy
title Prognostic role of apoptosis-related gene functional variants in advanced non-small-cell lung cancer patients treated with first-line platinum-based chemotherapy
title_full Prognostic role of apoptosis-related gene functional variants in advanced non-small-cell lung cancer patients treated with first-line platinum-based chemotherapy
title_fullStr Prognostic role of apoptosis-related gene functional variants in advanced non-small-cell lung cancer patients treated with first-line platinum-based chemotherapy
title_full_unstemmed Prognostic role of apoptosis-related gene functional variants in advanced non-small-cell lung cancer patients treated with first-line platinum-based chemotherapy
title_short Prognostic role of apoptosis-related gene functional variants in advanced non-small-cell lung cancer patients treated with first-line platinum-based chemotherapy
title_sort prognostic role of apoptosis-related gene functional variants in advanced non-small-cell lung cancer patients treated with first-line platinum-based chemotherapy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298310/
https://www.ncbi.nlm.nih.gov/pubmed/25609982
http://dx.doi.org/10.2147/OTT.S74855
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