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Prognostic assessment of apoptotic gene polymorphisms in non-small cell lung cancer in Chinese

Apoptosis plays a key role in inhibiting tumor growth, progression and resistance to anti-tumor therapy. We hypothesized that genetic variants in apoptotic genes may affect the prognosis of lung cancer. To test this hypothesis, we selected 38 potentially functional single nucleotide polymorphisms (S...

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Autores principales: Cao, Songyu, Wang, Cheng, Huang, Xinen, Dai, Juncheng, Hu, Lingmin, Liu, Yao, Chen, Jiaping, Ma, Hongxia, Jin, Guangfu, Hu, Zhibin, Xu, Lin, Shen, Hongbing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Department of Journal of Biomedical Research 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3664730/
https://www.ncbi.nlm.nih.gov/pubmed/23720679
http://dx.doi.org/10.7555/JBR.27.20130014
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author Cao, Songyu
Wang, Cheng
Huang, Xinen
Dai, Juncheng
Hu, Lingmin
Liu, Yao
Chen, Jiaping
Ma, Hongxia
Jin, Guangfu
Hu, Zhibin
Xu, Lin
Shen, Hongbing
author_facet Cao, Songyu
Wang, Cheng
Huang, Xinen
Dai, Juncheng
Hu, Lingmin
Liu, Yao
Chen, Jiaping
Ma, Hongxia
Jin, Guangfu
Hu, Zhibin
Xu, Lin
Shen, Hongbing
author_sort Cao, Songyu
collection PubMed
description Apoptosis plays a key role in inhibiting tumor growth, progression and resistance to anti-tumor therapy. We hypothesized that genetic variants in apoptotic genes may affect the prognosis of lung cancer. To test this hypothesis, we selected 38 potentially functional single nucleotide polymorphisms (SNPs) from 12 genes (BAX, BCL2, BID, CASP3, CASP6, CASP7, CASP8, CASP9, CASP10, FAS, FASLG and MCL1) involved in apoptosis to assess their prognostic significance in lung cancer in a Chinese case cohort with 568 non-small cell lung cancer (NSCLC) patients. Thirty-five SNPs passing quality control underwent association analyses, 11 of which were shown to be significantly associated with NSCLC survival (P < 0.05). After Cox stepwise regression analyses, 3 SNPs were independently associated with the outcome of NSCLC (BID rs8190315: P = 0.003; CASP9 rs4645981: P = 0.007 and FAS rs1800682: P = 0.016). A favorable survival of NSCLC was significantly associated with the genotypes of BID rs8190315 AG/GG (adjusted HR = 0.65, 95% CI: 0.49-0.88), CASP9 rs4645981 AA (HR = 0.22, 95% CI: 0.07-0.69) and FAS rs1800682 GG (adjusted HR = 0.67, 95% CI: 0.46-0.97). Time-dependent receptor operation curve (ROC) analysis revealed that the area under curve (AUC) at year 5 was significantly increased from 0.762 to 0.819 after adding the risk score of these 3 SNPs to the clinical risk score. The remaining 32 SNPs were not significantly associated with NSCLC prognosis after adjustment for these 3 SNPs. These findings indicate that BID rs8190315, CASP9 rs4645981 and FAS rs1800682 polymorphisms in the apoptotic pathway may be involved in the prognosis of NSCLC in the Chinese population.
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spelling pubmed-36647302013-05-29 Prognostic assessment of apoptotic gene polymorphisms in non-small cell lung cancer in Chinese Cao, Songyu Wang, Cheng Huang, Xinen Dai, Juncheng Hu, Lingmin Liu, Yao Chen, Jiaping Ma, Hongxia Jin, Guangfu Hu, Zhibin Xu, Lin Shen, Hongbing J Biomed Res Research Paper Apoptosis plays a key role in inhibiting tumor growth, progression and resistance to anti-tumor therapy. We hypothesized that genetic variants in apoptotic genes may affect the prognosis of lung cancer. To test this hypothesis, we selected 38 potentially functional single nucleotide polymorphisms (SNPs) from 12 genes (BAX, BCL2, BID, CASP3, CASP6, CASP7, CASP8, CASP9, CASP10, FAS, FASLG and MCL1) involved in apoptosis to assess their prognostic significance in lung cancer in a Chinese case cohort with 568 non-small cell lung cancer (NSCLC) patients. Thirty-five SNPs passing quality control underwent association analyses, 11 of which were shown to be significantly associated with NSCLC survival (P < 0.05). After Cox stepwise regression analyses, 3 SNPs were independently associated with the outcome of NSCLC (BID rs8190315: P = 0.003; CASP9 rs4645981: P = 0.007 and FAS rs1800682: P = 0.016). A favorable survival of NSCLC was significantly associated with the genotypes of BID rs8190315 AG/GG (adjusted HR = 0.65, 95% CI: 0.49-0.88), CASP9 rs4645981 AA (HR = 0.22, 95% CI: 0.07-0.69) and FAS rs1800682 GG (adjusted HR = 0.67, 95% CI: 0.46-0.97). Time-dependent receptor operation curve (ROC) analysis revealed that the area under curve (AUC) at year 5 was significantly increased from 0.762 to 0.819 after adding the risk score of these 3 SNPs to the clinical risk score. The remaining 32 SNPs were not significantly associated with NSCLC prognosis after adjustment for these 3 SNPs. These findings indicate that BID rs8190315, CASP9 rs4645981 and FAS rs1800682 polymorphisms in the apoptotic pathway may be involved in the prognosis of NSCLC in the Chinese population. Editorial Department of Journal of Biomedical Research 2013-05 2013-04-25 /pmc/articles/PMC3664730/ /pubmed/23720679 http://dx.doi.org/10.7555/JBR.27.20130014 Text en © 2013 by the Journal of Biomedical Research. All rights reserved.
spellingShingle Research Paper
Cao, Songyu
Wang, Cheng
Huang, Xinen
Dai, Juncheng
Hu, Lingmin
Liu, Yao
Chen, Jiaping
Ma, Hongxia
Jin, Guangfu
Hu, Zhibin
Xu, Lin
Shen, Hongbing
Prognostic assessment of apoptotic gene polymorphisms in non-small cell lung cancer in Chinese
title Prognostic assessment of apoptotic gene polymorphisms in non-small cell lung cancer in Chinese
title_full Prognostic assessment of apoptotic gene polymorphisms in non-small cell lung cancer in Chinese
title_fullStr Prognostic assessment of apoptotic gene polymorphisms in non-small cell lung cancer in Chinese
title_full_unstemmed Prognostic assessment of apoptotic gene polymorphisms in non-small cell lung cancer in Chinese
title_short Prognostic assessment of apoptotic gene polymorphisms in non-small cell lung cancer in Chinese
title_sort prognostic assessment of apoptotic gene polymorphisms in non-small cell lung cancer in chinese
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3664730/
https://www.ncbi.nlm.nih.gov/pubmed/23720679
http://dx.doi.org/10.7555/JBR.27.20130014
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