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Association of polymorphisms in interleukin-8 gene with cancer risk: a meta-analysis of 22 case–control studies
Interleukin-8 (IL-8) is a kind of chemokine that plays an important role in the development and progression of many human malignancies. Previous studies have uncovered that polymorphisms in IL-8 is associated with the risk of many cancer types, but the results were inconsistent and inconclusive. In...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4922774/ https://www.ncbi.nlm.nih.gov/pubmed/27382310 http://dx.doi.org/10.2147/OTT.S103159 |
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author | Zhang, Meng Fang, Tingting Wang, Kai Mei, Hongbing Lv, Zhaojie Wang, Feng Cai, Zhiming Liang, Chaozhao |
author_facet | Zhang, Meng Fang, Tingting Wang, Kai Mei, Hongbing Lv, Zhaojie Wang, Feng Cai, Zhiming Liang, Chaozhao |
author_sort | Zhang, Meng |
collection | PubMed |
description | Interleukin-8 (IL-8) is a kind of chemokine that plays an important role in the development and progression of many human malignancies. Previous studies have uncovered that polymorphisms in IL-8 is associated with the risk of many cancer types, but the results were inconsistent and inconclusive. In the present study, we aimed to explore the roles of IL-8 polymorphisms (rs2227307, rs2227306, +678T/C, rs1126647, and +1633C/T) and cancer risk through a systematic review and meta-analysis. Potential source of heterogeneity was sought out through sensitivity analysis. Desirable data were extracted and registered into databases. Finally, a total of ten publications comprising of 22 case–control studies, including 4,259 cases and 7,006 controls were ultimately eligible for the meta-analysis. No significant association was uncovered for all the five polymorphisms and the overall cancer risk. However, in the stratification analysis by cancer type, a significantly decreased risk of hepatocellular carcinoma was identified for rs2227306 polymorphism (T vs C: odds ratio [OR] =0.721, 95% confidence interval [CI] =0.567–0.916, P(z)=0.007; TT vs CC: OR =0.447, 95% CI =0.274–0.728, P(z)=0.001; TT vs TC + CC: OR =0.480, 95% CI =0.304–0.760, P(z)=0.002). In conclusion, our data shows that rs2227306 polymorphism plays a protective role in hepatocellular carcinoma risk. Future well-designed studies with a larger sample size are warranted to verify our findings. |
format | Online Article Text |
id | pubmed-4922774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49227742016-07-05 Association of polymorphisms in interleukin-8 gene with cancer risk: a meta-analysis of 22 case–control studies Zhang, Meng Fang, Tingting Wang, Kai Mei, Hongbing Lv, Zhaojie Wang, Feng Cai, Zhiming Liang, Chaozhao Onco Targets Ther Original Research Interleukin-8 (IL-8) is a kind of chemokine that plays an important role in the development and progression of many human malignancies. Previous studies have uncovered that polymorphisms in IL-8 is associated with the risk of many cancer types, but the results were inconsistent and inconclusive. In the present study, we aimed to explore the roles of IL-8 polymorphisms (rs2227307, rs2227306, +678T/C, rs1126647, and +1633C/T) and cancer risk through a systematic review and meta-analysis. Potential source of heterogeneity was sought out through sensitivity analysis. Desirable data were extracted and registered into databases. Finally, a total of ten publications comprising of 22 case–control studies, including 4,259 cases and 7,006 controls were ultimately eligible for the meta-analysis. No significant association was uncovered for all the five polymorphisms and the overall cancer risk. However, in the stratification analysis by cancer type, a significantly decreased risk of hepatocellular carcinoma was identified for rs2227306 polymorphism (T vs C: odds ratio [OR] =0.721, 95% confidence interval [CI] =0.567–0.916, P(z)=0.007; TT vs CC: OR =0.447, 95% CI =0.274–0.728, P(z)=0.001; TT vs TC + CC: OR =0.480, 95% CI =0.304–0.760, P(z)=0.002). In conclusion, our data shows that rs2227306 polymorphism plays a protective role in hepatocellular carcinoma risk. Future well-designed studies with a larger sample size are warranted to verify our findings. Dove Medical Press 2016-06-22 /pmc/articles/PMC4922774/ /pubmed/27382310 http://dx.doi.org/10.2147/OTT.S103159 Text en © 2016 Zhang 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 Zhang, Meng Fang, Tingting Wang, Kai Mei, Hongbing Lv, Zhaojie Wang, Feng Cai, Zhiming Liang, Chaozhao Association of polymorphisms in interleukin-8 gene with cancer risk: a meta-analysis of 22 case–control studies |
title | Association of polymorphisms in interleukin-8 gene with cancer risk: a meta-analysis of 22 case–control studies |
title_full | Association of polymorphisms in interleukin-8 gene with cancer risk: a meta-analysis of 22 case–control studies |
title_fullStr | Association of polymorphisms in interleukin-8 gene with cancer risk: a meta-analysis of 22 case–control studies |
title_full_unstemmed | Association of polymorphisms in interleukin-8 gene with cancer risk: a meta-analysis of 22 case–control studies |
title_short | Association of polymorphisms in interleukin-8 gene with cancer risk: a meta-analysis of 22 case–control studies |
title_sort | association of polymorphisms in interleukin-8 gene with cancer risk: a meta-analysis of 22 case–control studies |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4922774/ https://www.ncbi.nlm.nih.gov/pubmed/27382310 http://dx.doi.org/10.2147/OTT.S103159 |
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