Cargando…
Association between BHMT gene rs3733890 polymorphism and cancer risk: evidence from a meta-analysis
BACKGROUND AND OBJECTIVE: The gene betaine-homocysteine methyltransferase (BHMT) has drawn much attention during the past decades. An increasing number of clinical and genetic investigations have supposed that BHMT rs3733890 polymorphism might be associated with risk of breast cancer and ovarian can...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5001659/ https://www.ncbi.nlm.nih.gov/pubmed/27578989 http://dx.doi.org/10.2147/OTT.S103901 |
_version_ | 1782450461641539584 |
---|---|
author | Xu, Yue Yan, Cunye Hao, Zongyao Zhou, Jun Fan, Song Tai, Sheng Yang, Cheng Zhang, Li Liang, Chaozhao |
author_facet | Xu, Yue Yan, Cunye Hao, Zongyao Zhou, Jun Fan, Song Tai, Sheng Yang, Cheng Zhang, Li Liang, Chaozhao |
author_sort | Xu, Yue |
collection | PubMed |
description | BACKGROUND AND OBJECTIVE: The gene betaine-homocysteine methyltransferase (BHMT) has drawn much attention during the past decades. An increasing number of clinical and genetic investigations have supposed that BHMT rs3733890 polymorphism might be associated with risk of breast cancer and ovarian cancer. As no consistent conclusion has been achieved, we conducted an up-to-date summary of BHMT rs3733890 polymorphism and cancer risk through a meta-analysis. MATERIALS AND METHODS: The articles were collected from PubMed, Google Scholar, and CNKI (Chinese) databases up to December 2015. Then, the correlations were determined by reading the titles and abstracts and by further reading the full text to filter the unqualified articles. Odds ratio (OR) and the corresponding 95% confidence intervals (CI) were used to assess the results. RESULTS: Among 187 articles collected in the analysis, seven studies with a total of 2,832 cases and 3,958 controls were included for evaluation of the association between BHMT rs3733890 polymorphism and susceptibility of cancer risk. The heterogeneity test showed no significant differences. Furthermore, we found that BHMT −742G>A polymorphism in case and control groups showed no statistically significant association with susceptibility in various cancer types except for uterine cervical cancer (A vs G: OR =0.641, 95% CI =0.445–0.923, P=0.017; AA+AG vs GG: OR =0.579, 95% CI =0.362–0.924, P=0.022). In addition, no statistically significant association was uncovered when stratification analyses were conducted by ethnicity and genotyping methods. CONCLUSION: Our results have shown no obvious evidence that rs3733890 polymorphism in BHMT gene affected the susceptibility of head and neck squamous cell carcinoma, breast cancer, ovarian cancer, colorectal adenoma, and liver cancer. In contrast, we found the protective role of BHMT −742G>A polymorphism in uterine cervical cancer incidence. Future well-designed studies comprising larger sample size are warranted to verify our findings. |
format | Online Article Text |
id | pubmed-5001659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50016592016-08-30 Association between BHMT gene rs3733890 polymorphism and cancer risk: evidence from a meta-analysis Xu, Yue Yan, Cunye Hao, Zongyao Zhou, Jun Fan, Song Tai, Sheng Yang, Cheng Zhang, Li Liang, Chaozhao Onco Targets Ther Original Research BACKGROUND AND OBJECTIVE: The gene betaine-homocysteine methyltransferase (BHMT) has drawn much attention during the past decades. An increasing number of clinical and genetic investigations have supposed that BHMT rs3733890 polymorphism might be associated with risk of breast cancer and ovarian cancer. As no consistent conclusion has been achieved, we conducted an up-to-date summary of BHMT rs3733890 polymorphism and cancer risk through a meta-analysis. MATERIALS AND METHODS: The articles were collected from PubMed, Google Scholar, and CNKI (Chinese) databases up to December 2015. Then, the correlations were determined by reading the titles and abstracts and by further reading the full text to filter the unqualified articles. Odds ratio (OR) and the corresponding 95% confidence intervals (CI) were used to assess the results. RESULTS: Among 187 articles collected in the analysis, seven studies with a total of 2,832 cases and 3,958 controls were included for evaluation of the association between BHMT rs3733890 polymorphism and susceptibility of cancer risk. The heterogeneity test showed no significant differences. Furthermore, we found that BHMT −742G>A polymorphism in case and control groups showed no statistically significant association with susceptibility in various cancer types except for uterine cervical cancer (A vs G: OR =0.641, 95% CI =0.445–0.923, P=0.017; AA+AG vs GG: OR =0.579, 95% CI =0.362–0.924, P=0.022). In addition, no statistically significant association was uncovered when stratification analyses were conducted by ethnicity and genotyping methods. CONCLUSION: Our results have shown no obvious evidence that rs3733890 polymorphism in BHMT gene affected the susceptibility of head and neck squamous cell carcinoma, breast cancer, ovarian cancer, colorectal adenoma, and liver cancer. In contrast, we found the protective role of BHMT −742G>A polymorphism in uterine cervical cancer incidence. Future well-designed studies comprising larger sample size are warranted to verify our findings. Dove Medical Press 2016-08-22 /pmc/articles/PMC5001659/ /pubmed/27578989 http://dx.doi.org/10.2147/OTT.S103901 Text en © 2016 Xu 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 Xu, Yue Yan, Cunye Hao, Zongyao Zhou, Jun Fan, Song Tai, Sheng Yang, Cheng Zhang, Li Liang, Chaozhao Association between BHMT gene rs3733890 polymorphism and cancer risk: evidence from a meta-analysis |
title | Association between BHMT gene rs3733890 polymorphism and cancer risk: evidence from a meta-analysis |
title_full | Association between BHMT gene rs3733890 polymorphism and cancer risk: evidence from a meta-analysis |
title_fullStr | Association between BHMT gene rs3733890 polymorphism and cancer risk: evidence from a meta-analysis |
title_full_unstemmed | Association between BHMT gene rs3733890 polymorphism and cancer risk: evidence from a meta-analysis |
title_short | Association between BHMT gene rs3733890 polymorphism and cancer risk: evidence from a meta-analysis |
title_sort | association between bhmt gene rs3733890 polymorphism and cancer risk: evidence from a meta-analysis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5001659/ https://www.ncbi.nlm.nih.gov/pubmed/27578989 http://dx.doi.org/10.2147/OTT.S103901 |
work_keys_str_mv | AT xuyue associationbetweenbhmtgeners3733890polymorphismandcancerriskevidencefromametaanalysis AT yancunye associationbetweenbhmtgeners3733890polymorphismandcancerriskevidencefromametaanalysis AT haozongyao associationbetweenbhmtgeners3733890polymorphismandcancerriskevidencefromametaanalysis AT zhoujun associationbetweenbhmtgeners3733890polymorphismandcancerriskevidencefromametaanalysis AT fansong associationbetweenbhmtgeners3733890polymorphismandcancerriskevidencefromametaanalysis AT taisheng associationbetweenbhmtgeners3733890polymorphismandcancerriskevidencefromametaanalysis AT yangcheng associationbetweenbhmtgeners3733890polymorphismandcancerriskevidencefromametaanalysis AT zhangli associationbetweenbhmtgeners3733890polymorphismandcancerriskevidencefromametaanalysis AT liangchaozhao associationbetweenbhmtgeners3733890polymorphismandcancerriskevidencefromametaanalysis |