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Role of IL-1β 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 criter...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647244/ https://www.ncbi.nlm.nih.gov/pubmed/34861128 http://dx.doi.org/10.1177/03000605211060144 |
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author | Jafrin, Sarah Aziz, Md. Abdul Islam, Mohammad Safiqul |
author_facet | Jafrin, Sarah Aziz, Md. Abdul Islam, Mohammad Safiqul |
author_sort | Jafrin, Sarah |
collection | PubMed |
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 | Online Article Text |
id | pubmed-8647244 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-86472442021-12-07 Role of IL-1β rs1143634 (+3954C>T) polymorphism in cancer risk: an updated meta-analysis and trial sequential analysis Jafrin, Sarah Aziz, Md. Abdul Islam, Mohammad Safiqul J Int Med Res Meta-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 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). SAGE Publications 2021-12-03 /pmc/articles/PMC8647244/ /pubmed/34861128 http://dx.doi.org/10.1177/03000605211060144 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Meta-Analysis Jafrin, Sarah Aziz, Md. Abdul Islam, Mohammad Safiqul Role of IL-1β rs1143634 (+3954C>T) polymorphism in cancer risk: an updated meta-analysis and trial sequential analysis |
title | Role of IL-1β rs1143634 (+3954C>T) polymorphism
in cancer risk: an updated meta-analysis and trial sequential
analysis |
title_full | Role of IL-1β rs1143634 (+3954C>T) polymorphism
in cancer risk: an updated meta-analysis and trial sequential
analysis |
title_fullStr | Role of IL-1β rs1143634 (+3954C>T) polymorphism
in cancer risk: an updated meta-analysis and trial sequential
analysis |
title_full_unstemmed | Role of IL-1β rs1143634 (+3954C>T) polymorphism
in cancer risk: an updated meta-analysis and trial sequential
analysis |
title_short | Role of IL-1β rs1143634 (+3954C>T) polymorphism
in cancer risk: an updated meta-analysis and trial sequential
analysis |
title_sort | role of il-1β rs1143634 (+3954c>t) polymorphism
in cancer risk: an updated meta-analysis and trial sequential
analysis |
topic | Meta-Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647244/ https://www.ncbi.nlm.nih.gov/pubmed/34861128 http://dx.doi.org/10.1177/03000605211060144 |
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