Evidence map›Paper›PMID 29228747›Full record

ArticleOncotarget2017

The association of matrix metalloproteinase-9 promoter polymorphisms with gastric cancer risk: a meta-analysis.

Ziheng Peng, Jinhai Jia, Wenjian Gong, Xuehan Gao, Peiru Ma, Zhucheng Jin, Yue Fan, Yanchu Li, Xiaolin Zhang

Open access · diamondAbstract read
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Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 49% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 5 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Ziheng Peng *Department of School of Basic Medical Sciences, Hebei Medical University, Shi Jiazhuang 050017, China.
Jinhai Jia *Department of Outpatient Clinic, Hebei Medical University, Shi Jiazhuang 050017, China.
Wenjian GongDepartment of School of Basic Medical Sciences, Hebei Medical University, Shi Jiazhuang 050017, China.
Xuehan GaoDepartment of School of Basic Medical Sciences, Hebei Medical University, Shi Jiazhuang 050017, China.
Peiru MaDepartment of School of Basic Medical Sciences, Hebei Medical University, Shi Jiazhuang 050017, China.
Zhucheng JinDepartment of School of Basic Medical Sciences, Hebei Medical University, Shi Jiazhuang 050017, China.
Yue FanDepartment of School of Basic Medical Sciences, Hebei Medical University, Shi Jiazhuang 050017, China.
Yanchu LiDepartment of School of Basic Medical Sciences, Hebei Medical University, Shi Jiazhuang 050017, China.
Xiaolin ZhangDepartment of Epidemiology and Statistics, School of Public Health, Hebei Medical University, Shi Jiazhuang 050017, China.
Hebei Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeA variety of studies have observed that the single nucleotide polymorphisms (SNPs) matrix metalloproteinase-9 (MMP-9) gene may be associated with the risk of gastric cancer(GC), and a cytosine (C) to thymine (T) mutation at the -1562 site of the MMP-9 gene promoter is reported to be closely related to the susceptibility. However, because of the conflicting results of these studies, we undertook a systematic meta-analysis to assess the association between the SNPs and the risk of gastric cancer. MATERIALS AND

methodsA computerised literature search was conducted within the databases of PubMed, EMBASE, and ISI Web of Knowledge for studies on the genetic association of MMP-9-1562C/T and gastric cancer published from 2004 to 2015. The pooled odds ratio (OR) and 95% confidence intervals (CI) were estimated for each genotype using the dominant, recessive, co-dominant, and allelic models of the matrix metalloproteinase 9.

resultsOur analysis indicated a significant association of MMP-9-1562C/T with gastric cancer (dominant model [CT+TT/CC]: OR = 1.121, 95% CI = 0.965-1.304; recessive model [CC+CT/TT]: OR = 1.663, 95% CI = 1.148-2.408; co-dominant model [TT/CC]: OR = 1.666, 95% CI = 1.127-2.461; [CT/CC]: OR = 1.078, 95% CI = 0.923-1.259; allelic model [T/C]: OR = 1.150, 95% CI =1.014-1.304).

conclusionsOur meta-analysis results demonstrated that MMP-9-1562C/T promoter polymorphisms increase the risk of developing gastric cancer.

Indexed as

gastric cancermatrix metalloproteinase 9meta-analysispolymorphisms susceptibility risk

Identifiers

PMID29228747
PMCPMC5716787
OpenAlexW2754215859

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.