Cargando…
Association of polymorphisms in MALAT1 with the risk of esophageal squamous cell carcinoma in a Chinese population
OBJECTIVE: The main aim of this study was to investigate the association of polymorphisms in long non-coding RNA metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) with the risk of esophageal squamous cell carcinoma (ESCC) in a Chinese population. METHODS: A total of 245 ESCC patients a...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6452823/ https://www.ncbi.nlm.nih.gov/pubmed/31040692 http://dx.doi.org/10.2147/OTT.S191155 |
_version_ | 1783409353422798848 |
---|---|
author | Qu, Yan Shao, Na Yang, Wenjing Wang, Jianbo Cheng, Yufeng |
author_facet | Qu, Yan Shao, Na Yang, Wenjing Wang, Jianbo Cheng, Yufeng |
author_sort | Qu, Yan |
collection | PubMed |
description | OBJECTIVE: The main aim of this study was to investigate the association of polymorphisms in long non-coding RNA metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) with the risk of esophageal squamous cell carcinoma (ESCC) in a Chinese population. METHODS: A total of 245 ESCC patients and 490 gender- and age-matched cancer-free controls were genotyped for four tag single nucleotide polymorphisms (SNPs) of MALAT1 (rs3200401 C > T, rs1122709 C > G, rs664589 C > G, and rs619586 A > G). Statistical analyses including chi-squared test and logistic regression were performed to identify the association between the tag SNPs and risk of ESCC, and false discovery rate (FDR) <25% was applied to adjust for multiple comparisons. RESULTS: We found that rs3200401 C > T polymorphism of MALAT1 was significantly associated with increased risk of ESCC (CT vs CC: adjusted OR =1.59, 95% CI =1.07–2.35, P=0.021; TT vs CC: adjusted OR =2.27, 95% CI =1.04–4.96, P=0.039; dominant model [CT+TT vs CC]: adjusted OR =1.68, 95% CI =1.16–2.43, P=0.006). In the stratified analysis, rs3200401 TT and CT/TT genotypes were associated with increased risk of ESCC compared with CC genotype in subgroup of never drinking (TT vs CC: adjusted OR =2.34, 95% CI =1.02–5.34, P=0.044; CT/TT vs CC: adjusted OR =1.52, 95% CI =1.02–2.26, P=0.041). However, compared with AA genotype, MALAT1 rs619586 GG was associated with decreased risk of ESCC in ever drinking subgroup (GG vs AA: adjusted OR =0.38, 95% CI =0.15–0.99, P=0.049). The results remained significant after FDR adjustment (FDR value <0.25) except for the comparison between rs619586 GG and AA genotype in ever drinking subgroup. CONCLUSION: Taken together, our findings proposed that polymorphism rs3200401 C > T in MALAT1 gene is associated with increased risk of ESCC. Since the association between rs619586 A > G polymorphism and ESCC risk was not significant after FDR adjustment, there was a minor possibility that rs619586 A > G might be a protective factor for ESCC. |
format | Online Article Text |
id | pubmed-6452823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64528232019-04-30 Association of polymorphisms in MALAT1 with the risk of esophageal squamous cell carcinoma in a Chinese population Qu, Yan Shao, Na Yang, Wenjing Wang, Jianbo Cheng, Yufeng Onco Targets Ther Original Research OBJECTIVE: The main aim of this study was to investigate the association of polymorphisms in long non-coding RNA metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) with the risk of esophageal squamous cell carcinoma (ESCC) in a Chinese population. METHODS: A total of 245 ESCC patients and 490 gender- and age-matched cancer-free controls were genotyped for four tag single nucleotide polymorphisms (SNPs) of MALAT1 (rs3200401 C > T, rs1122709 C > G, rs664589 C > G, and rs619586 A > G). Statistical analyses including chi-squared test and logistic regression were performed to identify the association between the tag SNPs and risk of ESCC, and false discovery rate (FDR) <25% was applied to adjust for multiple comparisons. RESULTS: We found that rs3200401 C > T polymorphism of MALAT1 was significantly associated with increased risk of ESCC (CT vs CC: adjusted OR =1.59, 95% CI =1.07–2.35, P=0.021; TT vs CC: adjusted OR =2.27, 95% CI =1.04–4.96, P=0.039; dominant model [CT+TT vs CC]: adjusted OR =1.68, 95% CI =1.16–2.43, P=0.006). In the stratified analysis, rs3200401 TT and CT/TT genotypes were associated with increased risk of ESCC compared with CC genotype in subgroup of never drinking (TT vs CC: adjusted OR =2.34, 95% CI =1.02–5.34, P=0.044; CT/TT vs CC: adjusted OR =1.52, 95% CI =1.02–2.26, P=0.041). However, compared with AA genotype, MALAT1 rs619586 GG was associated with decreased risk of ESCC in ever drinking subgroup (GG vs AA: adjusted OR =0.38, 95% CI =0.15–0.99, P=0.049). The results remained significant after FDR adjustment (FDR value <0.25) except for the comparison between rs619586 GG and AA genotype in ever drinking subgroup. CONCLUSION: Taken together, our findings proposed that polymorphism rs3200401 C > T in MALAT1 gene is associated with increased risk of ESCC. Since the association between rs619586 A > G polymorphism and ESCC risk was not significant after FDR adjustment, there was a minor possibility that rs619586 A > G might be a protective factor for ESCC. Dove Medical Press 2019-04-03 /pmc/articles/PMC6452823/ /pubmed/31040692 http://dx.doi.org/10.2147/OTT.S191155 Text en © 2019 Qu et al. 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/). 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. |
spellingShingle | Original Research Qu, Yan Shao, Na Yang, Wenjing Wang, Jianbo Cheng, Yufeng Association of polymorphisms in MALAT1 with the risk of esophageal squamous cell carcinoma in a Chinese population |
title | Association of polymorphisms in MALAT1 with the risk of esophageal squamous cell carcinoma in a Chinese population |
title_full | Association of polymorphisms in MALAT1 with the risk of esophageal squamous cell carcinoma in a Chinese population |
title_fullStr | Association of polymorphisms in MALAT1 with the risk of esophageal squamous cell carcinoma in a Chinese population |
title_full_unstemmed | Association of polymorphisms in MALAT1 with the risk of esophageal squamous cell carcinoma in a Chinese population |
title_short | Association of polymorphisms in MALAT1 with the risk of esophageal squamous cell carcinoma in a Chinese population |
title_sort | association of polymorphisms in malat1 with the risk of esophageal squamous cell carcinoma in a chinese population |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6452823/ https://www.ncbi.nlm.nih.gov/pubmed/31040692 http://dx.doi.org/10.2147/OTT.S191155 |
work_keys_str_mv | AT quyan associationofpolymorphismsinmalat1withtheriskofesophagealsquamouscellcarcinomainachinesepopulation AT shaona associationofpolymorphismsinmalat1withtheriskofesophagealsquamouscellcarcinomainachinesepopulation AT yangwenjing associationofpolymorphismsinmalat1withtheriskofesophagealsquamouscellcarcinomainachinesepopulation AT wangjianbo associationofpolymorphismsinmalat1withtheriskofesophagealsquamouscellcarcinomainachinesepopulation AT chengyufeng associationofpolymorphismsinmalat1withtheriskofesophagealsquamouscellcarcinomainachinesepopulation |