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ABCC2-24C > T polymorphism is associated with the response to platinum/5-Fu-based neoadjuvant chemotherapy and better clinical outcomes in advanced gastric cancer patients
Several studies have evaluated the efficacy of neoadjuvant treatment using oxaliplatin and fluoropyrimidines in advanced gastric cancer (GC). However, preoperative biomarkers predictive of clinical outcome remain lacking. We examined polymorphisms in the MTHFR, DPYD, UMPS, ABCB1, ABCC2, GSTP1, ERCC1...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342428/ https://www.ncbi.nlm.nih.gov/pubmed/27487151 http://dx.doi.org/10.18632/oncotarget.10961 |
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author | Li, Ziyu Xing, Xiaofang Shan, Fei Li, Shuangxi Li, Zhongwu Xiao, Aitang Xing, Zhaodong Xue, Kan Li, Zhemin Hu, Ying Jia, Yongning Miao, Rulin Zhang, Lianhai Bu, Zhaode Wu, Aiwen Ji, Jiafu |
author_facet | Li, Ziyu Xing, Xiaofang Shan, Fei Li, Shuangxi Li, Zhongwu Xiao, Aitang Xing, Zhaodong Xue, Kan Li, Zhemin Hu, Ying Jia, Yongning Miao, Rulin Zhang, Lianhai Bu, Zhaode Wu, Aiwen Ji, Jiafu |
author_sort | Li, Ziyu |
collection | PubMed |
description | Several studies have evaluated the efficacy of neoadjuvant treatment using oxaliplatin and fluoropyrimidines in advanced gastric cancer (GC). However, preoperative biomarkers predictive of clinical outcome remain lacking. We examined polymorphisms in the MTHFR, DPYD, UMPS, ABCB1, ABCC2, GSTP1, ERCC1, and XRCC1 genes to evaluate their usefulness as pharmacogenetic markers in a cohort of 103 GC patients treated with preoperative chemotherapy. DNA was extracted from peripheral blood cells, and the genotypes were analyzed using a SNaPShot(TM) assay, polymerase chain reaction amplification, and sequencing. The ABCC2-24C > T (rs717620) genotype was associated with pathologic response to neoadjuvant chemotherapy. Patients with the TT and TC genotypes responded to neoadjuvant chemotherapy 3.80 times more often than those with the CC genotype (95% CI: 1.27–11.32). Patients with the CC genotype also had poorer outcomes than those with other genotypes. Thus, ABCC2-24C > T polymorphism may help to predict the response to preoperative chemotherapy in GC patients. |
format | Online Article Text |
id | pubmed-5342428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53424282017-03-22 ABCC2-24C > T polymorphism is associated with the response to platinum/5-Fu-based neoadjuvant chemotherapy and better clinical outcomes in advanced gastric cancer patients Li, Ziyu Xing, Xiaofang Shan, Fei Li, Shuangxi Li, Zhongwu Xiao, Aitang Xing, Zhaodong Xue, Kan Li, Zhemin Hu, Ying Jia, Yongning Miao, Rulin Zhang, Lianhai Bu, Zhaode Wu, Aiwen Ji, Jiafu Oncotarget Research Paper Several studies have evaluated the efficacy of neoadjuvant treatment using oxaliplatin and fluoropyrimidines in advanced gastric cancer (GC). However, preoperative biomarkers predictive of clinical outcome remain lacking. We examined polymorphisms in the MTHFR, DPYD, UMPS, ABCB1, ABCC2, GSTP1, ERCC1, and XRCC1 genes to evaluate their usefulness as pharmacogenetic markers in a cohort of 103 GC patients treated with preoperative chemotherapy. DNA was extracted from peripheral blood cells, and the genotypes were analyzed using a SNaPShot(TM) assay, polymerase chain reaction amplification, and sequencing. The ABCC2-24C > T (rs717620) genotype was associated with pathologic response to neoadjuvant chemotherapy. Patients with the TT and TC genotypes responded to neoadjuvant chemotherapy 3.80 times more often than those with the CC genotype (95% CI: 1.27–11.32). Patients with the CC genotype also had poorer outcomes than those with other genotypes. Thus, ABCC2-24C > T polymorphism may help to predict the response to preoperative chemotherapy in GC patients. Impact Journals LLC 2016-07-30 /pmc/articles/PMC5342428/ /pubmed/27487151 http://dx.doi.org/10.18632/oncotarget.10961 Text en Copyright: © 2016 Li et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Li, Ziyu Xing, Xiaofang Shan, Fei Li, Shuangxi Li, Zhongwu Xiao, Aitang Xing, Zhaodong Xue, Kan Li, Zhemin Hu, Ying Jia, Yongning Miao, Rulin Zhang, Lianhai Bu, Zhaode Wu, Aiwen Ji, Jiafu ABCC2-24C > T polymorphism is associated with the response to platinum/5-Fu-based neoadjuvant chemotherapy and better clinical outcomes in advanced gastric cancer patients |
title | ABCC2-24C > T polymorphism is associated with the response to platinum/5-Fu-based neoadjuvant chemotherapy and better clinical outcomes in advanced gastric cancer patients |
title_full | ABCC2-24C > T polymorphism is associated with the response to platinum/5-Fu-based neoadjuvant chemotherapy and better clinical outcomes in advanced gastric cancer patients |
title_fullStr | ABCC2-24C > T polymorphism is associated with the response to platinum/5-Fu-based neoadjuvant chemotherapy and better clinical outcomes in advanced gastric cancer patients |
title_full_unstemmed | ABCC2-24C > T polymorphism is associated with the response to platinum/5-Fu-based neoadjuvant chemotherapy and better clinical outcomes in advanced gastric cancer patients |
title_short | ABCC2-24C > T polymorphism is associated with the response to platinum/5-Fu-based neoadjuvant chemotherapy and better clinical outcomes in advanced gastric cancer patients |
title_sort | abcc2-24c > t polymorphism is associated with the response to platinum/5-fu-based neoadjuvant chemotherapy and better clinical outcomes in advanced gastric cancer patients |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342428/ https://www.ncbi.nlm.nih.gov/pubmed/27487151 http://dx.doi.org/10.18632/oncotarget.10961 |
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