Evidence map›Paper›PMID 25268356›Full record

ArticlePloS one2014

The CXCL12 G801A polymorphism is associated with cancer risk: a meta-analysis.

Ke Zhu, Benchun Jiang, Rong Hu, Ying Yang, Miao Miao, Yingchun Li, Zhuogang Liu

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 3 pooled it
–field-weighted citation impact
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

9 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Review
  6. Article
  7. Article
  8. OncoTargets and therapy · 2017
    Article
  9. Article
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

7 authors.

Ke ZhuDepartment of Hematology, Affiliated Shengjing Hospital, China Medical University, Shenyang, Liaoning, China.
Benchun JiangDepartment of General Surgery, Affiliated Shengjing Hospital, China Medical University, Shenyang, Liaoning, China.
Rong HuDepartment of Hematology, Affiliated Shengjing Hospital, China Medical University, Shenyang, Liaoning, China.
Ying YangDepartment of Hematology, Affiliated Shengjing Hospital, China Medical University, Shenyang, Liaoning, China.
Miao MiaoDepartment of Hematology, Affiliated Shengjing Hospital, China Medical University, Shenyang, Liaoning, China.
Yingchun LiDepartment of Hematology, Affiliated Shengjing Hospital, China Medical University, Shenyang, Liaoning, China.
Zhuogang LiuDepartment of Hematology, Affiliated Shengjing Hospital, China Medical University, Shenyang, Liaoning, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCXCL12 is a small chemotactic cytokine belonging to the CXC chemokine family expressed in various organs. It contributes to the migration, invasion and angiogenesis of cancer cells. Recently, the CXCL12 G801A polymorphism was shown to be associated with an increased risk of various kinds of cancers, but the results were too inconsistent to be conclusive.

methodsTo solve the problem of inadequate statistical power and conflicting results, a meta-analysis of published case-control studies was performed, including 4,435 cancer cases and 6,898 controls. Odds ratios (ORs) and their 95% confidence intervals (CIs) were used to determine the strength of association between CXCL12 G801A polymorphism and cancer risk.

resultsA significant association between CXCL12 G801A polymorphism and cancer risk was found under all genetic models. Further, subgroup analysis stratified by ethnicity suggested a significant association between CXCL12 G801A polymorphism and cancer risk in the Asian subgroup under all genetic models. However, in the Caucasian subgroup, a significant association was only found under an additive genetic model and a dominant genetic model. The analysis stratified by cancer type found that CXCL12 G801A polymorphism may increase the risk of breast cancer, lung cancer, and "other" cancers. Based on subgroup stratified by source of controls, a significant association was observed in hospital-based studies under all genetic models.

conclusionsThe CXCL12 G801A polymorphism is associated with an increased risk of cancer based on current published data. In the future, large-scale well-designed studies with more information are needed to better estimate possible gene-gene or gene-environment interactions.

Indexed as

Polymorphism, Single NucleotideAsian PeopleBreast NeoplasmsCase-Control StudiesChemokine CXCL12Gene ExpressionHumansLung NeoplasmsModels, GeneticOdds RatioRiskWhite PeopleChemokine CXCL12CXCL12 protein, human

Identifiers

PMID25268356
PMCPMC4182572

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.