Evidence map›Paper›PMID 33817070›Full record

ArticleOpen life sciences2018

IL-17 Gene Rs3748067 C>T Polymorphism and Gastric Cancer Risk: A Meta-analysis.

Wang Ying, Yu Yingcong, You Liyi, Zheng Liang

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Article in Open life sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Wang YingDepartment of Gastroenterology, Wenzhou People's Hospital, Wenzhou Zhejiang Province, 325000 PR, China.
Yu YingcongDepartment of Gastroenterology, Wenzhou People's Hospital, Wenzhou Zhejiang Province, 325000 PR, China.
You LiyiDepartment of Ultrasonography, Wenzhou People's Hospital, Wenzhou Zhejiang Province, 325000 PR, China.
Zheng LiangDepartment of Gastroenterology, Wenzhou People's Hospital, Wenzhou Zhejiang Province, 325000 PR, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe purpose of this study was to investigate the correlation between Interleukin 17 (IL-17) gene rs3748067 C>T polymorphism and gastric cancer risk through pooling the open published data.

methodCase-control or cohort studies relevant to IL-17 gene rs3748067 C>T polymorphism and gastric cancer susceptibility were systematic searched for in the databases of CNKI, Pubmed, Medline, Embase and Web of science. The association between IL-17 gene rs3748067 C>T polymorphism and gastric cancer risk were expressed with an odds ratio(OR) and 95% confidence interval (95% CI). Statistical heterogeneity across the studies was evaluated by I2 test. Publication bias was evaluated by Begg's funnel plot and Egger's line regression test.

resultsFinally, seven case-control studies were included in our present study. Because of the statistical heterogeneity among the included studies for the aspects of dominant (TT+CT vs CC), recessive (TT vs CT+CC) and homozygous genetic model (TT vs CC), the data was pooled by random effect model. The pooled ORs were OR=0.99 (95% CI: 0.65-1.52), OR =1.23 (95% CI: 0.73-2.06 ) and OR=1.14 (95% CI: 0.58-2.27) for dominant, recessive and homozygous genetic model respectively. The pooled data indicated no correlation between IL-17 gene rs3748067 C>T polymorphism and gastric cancer risk. Significant publication bias was found in the dominant genetic model (p<0.05), but not in recessive and homozygous genetic model (p>0.05).

conclusionBased on the present evidence, there was no correlation between IL-17 gene rs3748067 C>T polymorphism and gastric cancer susceptibility in all genetic model. However, for the small sample size, significant heterogeneity and publication bias, the conclusion should be further evaluated through well designed case-control or cohort studies.

Indexed as

Gastric cancerIL-17meta-analysisPolymorphismsusceptibility

Identifiers

PMID33817070
PMCPMC7874690

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