Role of rs1143634 (+3954C>T) polymorphism in cancer risk: an updated meta-analysis and trial sequential analysis
Objective Oxidative stress caused by the pro-inflammatory cytokine interleukin (IL)-1β has been widely investigated for cancer risk. In this study, we focused on the role of IL-1β rs1143634 polymorphism to reveal its impact on cancer development. Methods Related studies with fixed inclusion criteria...
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oai:doaj.org-article:ae7156c626874535999a6e37d3e2d2752021-12-04T01:03:31ZRole of rs1143634 (+3954C>T) polymorphism in cancer risk: an updated meta-analysis and trial sequential analysis1473-230010.1177/03000605211060144https://doaj.org/article/ae7156c626874535999a6e37d3e2d2752021-12-01T00:00:00Zhttps://doi.org/10.1177/03000605211060144https://doaj.org/toc/1473-2300Objective Oxidative stress caused by the pro-inflammatory cytokine interleukin (IL)-1β has been widely investigated for cancer risk. In this study, we focused on the role of IL-1β rs1143634 polymorphism to reveal its impact on cancer development. Methods Related studies with fixed inclusion criteria were selected from electronic databases to May 2021. This meta-analysis was performed with odds ratios and 95% confidence intervals. Heterogeneity, publication bias and sensitivity analyses were also conducted. Trial sequential analysis (TSA) and in - silico gene expression analysis were performed. Results Forty-four case–control studies involving 18,645 patients with cancer and 22,882 controls were included. We observed a significant association of this single nucleotide polymorphism with overall cancer risk in the codominant model 3 (1.13-fold), recessive model (1.14-fold) and allelic model (1.08-fold). Subgroup analysis revealed that rs1143634 elevated the risk of gastric cancer, breast cancer and multiple myeloma. In addition, Asian and mixed populations and hospital-based controls had a significantly higher risk of cancer development. TSA confirmed our findings. Conclusion Our meta-analysis revealed that the presence of IL-1β rs1143634 polymorphism increases the risk of cancer development. Among polymorphism carriers, the Asian population has a higher risk than other ethnic populations. This meta-analysis was registered retrospectively at INPLASY ( https://inplasy.com/ , INPLASY2021100044).Sarah JafrinMd. Abdul AzizMohammad Safiqul IslamSAGE PublishingarticleMedicine (General)R5-920ENJournal of International Medical Research, Vol 49 (2021) |
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Medicine (General) R5-920 Sarah Jafrin Md. Abdul Aziz Mohammad Safiqul Islam Role of rs1143634 (+3954C>T) polymorphism in cancer risk: an updated meta-analysis and trial sequential analysis |
description |
Objective Oxidative stress caused by the pro-inflammatory cytokine interleukin (IL)-1β has been widely investigated for cancer risk. In this study, we focused on the role of IL-1β rs1143634 polymorphism to reveal its impact on cancer development. Methods Related studies with fixed inclusion criteria were selected from electronic databases to May 2021. This meta-analysis was performed with odds ratios and 95% confidence intervals. Heterogeneity, publication bias and sensitivity analyses were also conducted. Trial sequential analysis (TSA) and in - silico gene expression analysis were performed. Results Forty-four case–control studies involving 18,645 patients with cancer and 22,882 controls were included. We observed a significant association of this single nucleotide polymorphism with overall cancer risk in the codominant model 3 (1.13-fold), recessive model (1.14-fold) and allelic model (1.08-fold). Subgroup analysis revealed that rs1143634 elevated the risk of gastric cancer, breast cancer and multiple myeloma. In addition, Asian and mixed populations and hospital-based controls had a significantly higher risk of cancer development. TSA confirmed our findings. Conclusion Our meta-analysis revealed that the presence of IL-1β rs1143634 polymorphism increases the risk of cancer development. Among polymorphism carriers, the Asian population has a higher risk than other ethnic populations. This meta-analysis was registered retrospectively at INPLASY ( https://inplasy.com/ , INPLASY2021100044). |
format |
article |
author |
Sarah Jafrin Md. Abdul Aziz Mohammad Safiqul Islam |
author_facet |
Sarah Jafrin Md. Abdul Aziz Mohammad Safiqul Islam |
author_sort |
Sarah Jafrin |
title |
Role of rs1143634 (+3954C>T) polymorphism in cancer risk: an updated meta-analysis and trial sequential analysis |
title_short |
Role of rs1143634 (+3954C>T) polymorphism in cancer risk: an updated meta-analysis and trial sequential analysis |
title_full |
Role of rs1143634 (+3954C>T) polymorphism in cancer risk: an updated meta-analysis and trial sequential analysis |
title_fullStr |
Role of rs1143634 (+3954C>T) polymorphism in cancer risk: an updated meta-analysis and trial sequential analysis |
title_full_unstemmed |
Role of rs1143634 (+3954C>T) polymorphism in cancer risk: an updated meta-analysis and trial sequential analysis |
title_sort |
role of rs1143634 (+3954c>t) polymorphism in cancer risk: an updated meta-analysis and trial sequential analysis |
publisher |
SAGE Publishing |
publishDate |
2021 |
url |
https://doaj.org/article/ae7156c626874535999a6e37d3e2d275 |
work_keys_str_mv |
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