Cargando…

Polymorphism in miR-146a associated with clinical characteristics and outcomes in gastric cancer patients treated with adjuvant oxaliplatin and fluoropyrimidines

PURPOSE: Polymorphism in miR-146a (rs2910164) has been reported to be associated with gastric cancer risk in the Chinese population. We aimed at evaluating the relationship between rs2910164 and the clinical characteristics and outcomes in stage IB–III gastric cancer patients treated with adjuvant c...

Descripción completa

Detalles Bibliográficos
Autores principales: Liao, Yu-Qian, Liao, Yu-Lu, Li, Jun, Peng, Li-Xiang, Wan, Yi-Ye, Zhong, Rui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4577269/
https://www.ncbi.nlm.nih.gov/pubmed/26396533
http://dx.doi.org/10.2147/OTT.S89635
_version_ 1782390961672814592
author Liao, Yu-Qian
Liao, Yu-Lu
Li, Jun
Peng, Li-Xiang
Wan, Yi-Ye
Zhong, Rui
author_facet Liao, Yu-Qian
Liao, Yu-Lu
Li, Jun
Peng, Li-Xiang
Wan, Yi-Ye
Zhong, Rui
author_sort Liao, Yu-Qian
collection PubMed
description PURPOSE: Polymorphism in miR-146a (rs2910164) has been reported to be associated with gastric cancer risk in the Chinese population. We aimed at evaluating the relationship between rs2910164 and the clinical characteristics and outcomes in stage IB–III gastric cancer patients treated with adjuvant chemotherapy after surgery. MATERIALS AND METHODS: Ninety-eight patients with stage IB–III gastric cancer treated with surgical resection followed by adjuvant chemotherapy of oxaliplatin and fluoropyrimidines were included in the analysis. Genomic DNA was extracted from peripheral blood sample of all patients. Polymerase chain reaction-based restriction fragment length polymorphism assay was used to determine the genotypes. RESULTS: The 2-year disease-free survival rate was 63%, and the 3-year overall survival (OS) rate was 73.4%. In dominant model, we found that rs2910164 GC + CC (G: guanine, C: cytosine) genotype carriers were less likely to develop lymph node metastasis (P=0.059). The 3-year OS was significantly different for patients with or without lymph node metastasis (89.3% vs 63.7%, P=0.015) and for patients with stage I–III disease (100.0%, 88.6%, and 56.9%; P=0.018). The 3-year OS for GC + CC carriers was significantly higher than for GG carriers (75.1% vs 66.7%, P=0.041). After the multivariant Cox regression analysis, histological grade (P=0.033, relative risk: 5.116, 95% confidence interval: 1.145–22.865) and lymph node status (P=0.031, relative risk: 6.648, 95% confidence interval: 1.191–37.118) were found to be independent prognostic factors for these patients. CONCLUSION: rs2910164 could be associated with the lymph node metastasis and prognosis of Chinese gastric cancer patients treated with oxaliplatin and fluoropyrimidines after surgical resection.
format Online
Article
Text
id pubmed-4577269
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-45772692015-09-22 Polymorphism in miR-146a associated with clinical characteristics and outcomes in gastric cancer patients treated with adjuvant oxaliplatin and fluoropyrimidines Liao, Yu-Qian Liao, Yu-Lu Li, Jun Peng, Li-Xiang Wan, Yi-Ye Zhong, Rui Onco Targets Ther Original Research PURPOSE: Polymorphism in miR-146a (rs2910164) has been reported to be associated with gastric cancer risk in the Chinese population. We aimed at evaluating the relationship between rs2910164 and the clinical characteristics and outcomes in stage IB–III gastric cancer patients treated with adjuvant chemotherapy after surgery. MATERIALS AND METHODS: Ninety-eight patients with stage IB–III gastric cancer treated with surgical resection followed by adjuvant chemotherapy of oxaliplatin and fluoropyrimidines were included in the analysis. Genomic DNA was extracted from peripheral blood sample of all patients. Polymerase chain reaction-based restriction fragment length polymorphism assay was used to determine the genotypes. RESULTS: The 2-year disease-free survival rate was 63%, and the 3-year overall survival (OS) rate was 73.4%. In dominant model, we found that rs2910164 GC + CC (G: guanine, C: cytosine) genotype carriers were less likely to develop lymph node metastasis (P=0.059). The 3-year OS was significantly different for patients with or without lymph node metastasis (89.3% vs 63.7%, P=0.015) and for patients with stage I–III disease (100.0%, 88.6%, and 56.9%; P=0.018). The 3-year OS for GC + CC carriers was significantly higher than for GG carriers (75.1% vs 66.7%, P=0.041). After the multivariant Cox regression analysis, histological grade (P=0.033, relative risk: 5.116, 95% confidence interval: 1.145–22.865) and lymph node status (P=0.031, relative risk: 6.648, 95% confidence interval: 1.191–37.118) were found to be independent prognostic factors for these patients. CONCLUSION: rs2910164 could be associated with the lymph node metastasis and prognosis of Chinese gastric cancer patients treated with oxaliplatin and fluoropyrimidines after surgical resection. Dove Medical Press 2015-09-16 /pmc/articles/PMC4577269/ /pubmed/26396533 http://dx.doi.org/10.2147/OTT.S89635 Text en © 2015 Liao 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
Liao, Yu-Qian
Liao, Yu-Lu
Li, Jun
Peng, Li-Xiang
Wan, Yi-Ye
Zhong, Rui
Polymorphism in miR-146a associated with clinical characteristics and outcomes in gastric cancer patients treated with adjuvant oxaliplatin and fluoropyrimidines
title Polymorphism in miR-146a associated with clinical characteristics and outcomes in gastric cancer patients treated with adjuvant oxaliplatin and fluoropyrimidines
title_full Polymorphism in miR-146a associated with clinical characteristics and outcomes in gastric cancer patients treated with adjuvant oxaliplatin and fluoropyrimidines
title_fullStr Polymorphism in miR-146a associated with clinical characteristics and outcomes in gastric cancer patients treated with adjuvant oxaliplatin and fluoropyrimidines
title_full_unstemmed Polymorphism in miR-146a associated with clinical characteristics and outcomes in gastric cancer patients treated with adjuvant oxaliplatin and fluoropyrimidines
title_short Polymorphism in miR-146a associated with clinical characteristics and outcomes in gastric cancer patients treated with adjuvant oxaliplatin and fluoropyrimidines
title_sort polymorphism in mir-146a associated with clinical characteristics and outcomes in gastric cancer patients treated with adjuvant oxaliplatin and fluoropyrimidines
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4577269/
https://www.ncbi.nlm.nih.gov/pubmed/26396533
http://dx.doi.org/10.2147/OTT.S89635
work_keys_str_mv AT liaoyuqian polymorphisminmir146aassociatedwithclinicalcharacteristicsandoutcomesingastriccancerpatientstreatedwithadjuvantoxaliplatinandfluoropyrimidines
AT liaoyulu polymorphisminmir146aassociatedwithclinicalcharacteristicsandoutcomesingastriccancerpatientstreatedwithadjuvantoxaliplatinandfluoropyrimidines
AT lijun polymorphisminmir146aassociatedwithclinicalcharacteristicsandoutcomesingastriccancerpatientstreatedwithadjuvantoxaliplatinandfluoropyrimidines
AT penglixiang polymorphisminmir146aassociatedwithclinicalcharacteristicsandoutcomesingastriccancerpatientstreatedwithadjuvantoxaliplatinandfluoropyrimidines
AT wanyiye polymorphisminmir146aassociatedwithclinicalcharacteristicsandoutcomesingastriccancerpatientstreatedwithadjuvantoxaliplatinandfluoropyrimidines
AT zhongrui polymorphisminmir146aassociatedwithclinicalcharacteristicsandoutcomesingastriccancerpatientstreatedwithadjuvantoxaliplatinandfluoropyrimidines