Evidence map›Paper›PMID 42583819›Full record

SynthesisGenes, chromosomes & cancer2026

The Contribution of CD133 Gene Polymorphisms to Cancer Risk: Integrating Case-Control Evidence With Meta-Analysis.

Xinyi Zhang, Hang Zhou, Yongwei Li, Yuping Chu, Boyu Li, Jiaxuan Dai, Qinyue Yang, Xianhong Feng, Bifeng Chen

Abstract readMeta-Analysis
In one paragraph

Synthesis in Genes, chromosomes & cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Xinyi ZhangDepartment of Biological Science and Technology, School of Chemistry, Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan, Hubei, China.
Hang ZhouInstitute of WUT-AMU, Wuhan University of Technology, Wuhan, Hubei, China.
Yongwei LiInstitute of WUT-AMU, Wuhan University of Technology, Wuhan, Hubei, China.
Yuping ChuInstitute of WUT-AMU, Wuhan University of Technology, Wuhan, Hubei, China.
Boyu LiDepartment of Biological Science and Technology, School of Chemistry, Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan, Hubei, China.
Jiaxuan DaiDepartment of Biological Science and Technology, School of Chemistry, Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan, Hubei, China.
Qinyue YangDepartment of Biological Science and Technology, School of Chemistry, Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan, Hubei, China.
Xianhong FengDepartment of Clinical Laboratory, Wuhan Xinzhou District People's Hospital, Wuhan, Hubei, China.
Bifeng ChenDepartment of Biological Science and Technology, School of Chemistry, Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan, Hubei, China.ORCID https://orcid.org/0000-0001-5482-1910

Funding

Fundamental Research Funds for the Central Universities WUT: 104972026KFYjc0071Horizontal Project WUT: 202401hx0157Horizontal Project WUT: 202501hx0176
6 · The paper itself

Abstract

Previous studies have extensively examined the associations between CD133 gene polymorphisms (rs10022537, rs2286455, rs2240688, and rs3130) and cancer risk, but have yielded inconsistent results. This study aimed to investigate the potential contributions of these polymorphisms to the susceptibility of liver, lung, and gastric cancers through a replicated case-control study and a subsequent systematic meta-analysis. A total of 480 patients with liver cancer, 550 patients with lung cancer, 460 patients with gastric cancer, and 800 healthy controls from the Hubei population were enrolled. Sanger sequencing assay was applied to genotype the four target CD133 gene polymorphisms. The case-control study revealed that rs10022537 was significantly associated with the risk of liver cancer but not with the risk of lung or gastric cancer. In contrast, rs3130 was significantly associated with both lung and liver cancer risk, whereas no association was observed with gastric cancer risk. rs2240688 exhibited a significant association exclusively with lung cancer risk, and rs2286455 showed no significant association with any of the three cancer types. The meta-analysis further demonstrated that rs3130 was significantly associated with lung cancer risk in the Chinese population, and rs2240688 was significantly associated with gastric cancer risk. No significant association was found for rs10022537 or rs2286455 with liver, lung, or gastric cancer risk. Collectively, these findings suggested that rs3130 and rs2240688 in the CD133 gene may serve as susceptibility factors for risk of lung cancer and gastric cancer, respectively. Further validation studies in larger and more diverse populations are warranted.

Indexed as

AC133 AntigenLiver NeoplasmsLung NeoplasmsPolymorphism, Single NucleotideStomach NeoplasmsAgedCase-Control StudiesFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedAC133 AntigenPROM1 protein, humancancer riskcase–control studyCD133 genemeta‐analysissingle‐nucleotide polymorphism

Identifiers

PMID42583819
PMCPMC13463280

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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.