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ARLTS1 polymorphism is associated with an increased risk of familial cancer: evidence from a meta-analysis
Adenosine diphosphate (ADP)-ribosylation factor-like tumour suppressor gene 1(ARLTS1) might be associated with an increased risk of several types of familial cancers. However, previous studies have shown that cancer susceptibility is not completely consistent with ARLTS1 polymorphisms, and the preci...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470195/ https://www.ncbi.nlm.nih.gov/pubmed/28630657 http://dx.doi.org/10.1186/s13053-017-0068-7 |
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author | Jiang, Yan Zhao, Chen-Yang Cheng, Li-Chun Xu, Bing Lv, Hui-Yi |
author_facet | Jiang, Yan Zhao, Chen-Yang Cheng, Li-Chun Xu, Bing Lv, Hui-Yi |
author_sort | Jiang, Yan |
collection | PubMed |
description | Adenosine diphosphate (ADP)-ribosylation factor-like tumour suppressor gene 1(ARLTS1) might be associated with an increased risk of several types of familial cancers. However, previous studies have shown that cancer susceptibility is not completely consistent with ARLTS1 polymorphisms, and the precise mechanism remains unknown. Therefore, we conducted a meta-analysis of case-control studies by searching the PubMed, Embase, OVID, Science Direct and Chinese National Knowledge Infrastructure (CNKI) databases. In total, 12 studies met the inclusion criteria and were included in this meta-analysis. Statistical analyses were performed using STATA 11.0 software. Overall, the Cys148Arg T > C variant significantly increased cancer risk (CC vs. TT: OR = 1.27, 95% CI = 1.15–1.41, P < 0.05). The stratification indicated that the Cys148Arg variant is significantly associated with sporadic cancer (CC vs. TT: OR = 1.36, 95% CI = 1.18–1.55) and familial cancer (CC vs. TT: OR = 1.26, 95% CI = 1.12–1.43). Trp149Stop, Pro131Leu, Ser99Ser and Leu132Leu were not correlated with cancer susceptibility. Based on these results, we demonstrated that the ARLTS1 Cys148Arg polymorphism is associated with an increased risk of sporadic cancer and familial cancer, and there were no associations between the other four SNPs (i.e., Trp149Stop, Pro131Leu, Ser99Ser and Leu132Leu) and cancer risk. |
format | Online Article Text |
id | pubmed-5470195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54701952017-06-19 ARLTS1 polymorphism is associated with an increased risk of familial cancer: evidence from a meta-analysis Jiang, Yan Zhao, Chen-Yang Cheng, Li-Chun Xu, Bing Lv, Hui-Yi Hered Cancer Clin Pract Review Adenosine diphosphate (ADP)-ribosylation factor-like tumour suppressor gene 1(ARLTS1) might be associated with an increased risk of several types of familial cancers. However, previous studies have shown that cancer susceptibility is not completely consistent with ARLTS1 polymorphisms, and the precise mechanism remains unknown. Therefore, we conducted a meta-analysis of case-control studies by searching the PubMed, Embase, OVID, Science Direct and Chinese National Knowledge Infrastructure (CNKI) databases. In total, 12 studies met the inclusion criteria and were included in this meta-analysis. Statistical analyses were performed using STATA 11.0 software. Overall, the Cys148Arg T > C variant significantly increased cancer risk (CC vs. TT: OR = 1.27, 95% CI = 1.15–1.41, P < 0.05). The stratification indicated that the Cys148Arg variant is significantly associated with sporadic cancer (CC vs. TT: OR = 1.36, 95% CI = 1.18–1.55) and familial cancer (CC vs. TT: OR = 1.26, 95% CI = 1.12–1.43). Trp149Stop, Pro131Leu, Ser99Ser and Leu132Leu were not correlated with cancer susceptibility. Based on these results, we demonstrated that the ARLTS1 Cys148Arg polymorphism is associated with an increased risk of sporadic cancer and familial cancer, and there were no associations between the other four SNPs (i.e., Trp149Stop, Pro131Leu, Ser99Ser and Leu132Leu) and cancer risk. BioMed Central 2017-06-13 /pmc/articles/PMC5470195/ /pubmed/28630657 http://dx.doi.org/10.1186/s13053-017-0068-7 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Jiang, Yan Zhao, Chen-Yang Cheng, Li-Chun Xu, Bing Lv, Hui-Yi ARLTS1 polymorphism is associated with an increased risk of familial cancer: evidence from a meta-analysis |
title | ARLTS1 polymorphism is associated with an increased risk of familial cancer: evidence from a meta-analysis |
title_full | ARLTS1 polymorphism is associated with an increased risk of familial cancer: evidence from a meta-analysis |
title_fullStr | ARLTS1 polymorphism is associated with an increased risk of familial cancer: evidence from a meta-analysis |
title_full_unstemmed | ARLTS1 polymorphism is associated with an increased risk of familial cancer: evidence from a meta-analysis |
title_short | ARLTS1 polymorphism is associated with an increased risk of familial cancer: evidence from a meta-analysis |
title_sort | arlts1 polymorphism is associated with an increased risk of familial cancer: evidence from a meta-analysis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470195/ https://www.ncbi.nlm.nih.gov/pubmed/28630657 http://dx.doi.org/10.1186/s13053-017-0068-7 |
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