Evidence map›Paper›PMID 40542752›Full record

SynthesisAsian Pacific journal of cancer prevention : APJCP2025

Correlation of VEGF +405C/G Polymorphism with Gastrointestinal Tract Cancers Risk: An Updated Meta-Analysis.

Sukhpreet Kaur Walia, Vasudha Sambyal, Kamlesh Guleria

Abstract readMeta-Analysis
In one paragraph

Synthesis in Asian Pacific journal of cancer prevention : APJCP, 2025. 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

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Sukhpreet Kaur WaliaHuman Cytogenetics Laboratory, Department of Human Genetics, Guru Nanak Dev University, Amritsar 143005, Punjab, India.
Vasudha SambyalHuman Cytogenetics Laboratory, Department of Human Genetics, Guru Nanak Dev University, Amritsar 143005, Punjab, India.
Kamlesh GuleriaHuman Cytogenetics Laboratory, Department of Human Genetics, Guru Nanak Dev University, Amritsar 143005, Punjab, India.ORCID 0000-0002-1626-601X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe functional polymorphisms of VEGF can affect different cellular processes and play a major role in angiogenesis and tumor development. Several case-control studies have explored the association of VEGF +405C/G polymorphism with GIT cancer risk, however, the results were inconsistent. Therefore, the meta-analysis was conducted to clarify the association.

methodsBased on the inclusion and exclusion criteria, relevant data were extracted from PubMed, Google Scholar, Web of Science and Science Direct. Twenty three studies comprising 5,656 cases and 6,319 healthy controls were included in the present meta-analysis and the data was analysed by using online MetaGenyo software.

resultsIn the present study, no significant association was found in any of the genetic models in overall analysis as well as when data was stratified according to the ethnicity (p>0.05). After performing sub-group analysis on the basis of cancer type, significant association was found with increased risk of developing esophageal cancer under allele contrast, recessive, GG vs. CC and GG vs. GC models (p<0.05). Under overdominant model, VEGF +405C/G polymorphism was significantly associated with decreased risk of developing esophageal cancer (p=0.017) and GG vs. GC model showed a significant association with the risk of developing colorectal cancer (p=0.047) and pancreatic cancer (p=0.010). However, GC vs. CC model showed that VEGF +405C/G polymorphism was significantly associated with reduced risk of pancreatic cancer (p=0.039).

conclusionThe present updated meta-analysis suggested that VEGF +405C/G polymorphism may serve as a biomarker for determining an individual's risk of esophageal, colorectal and pancreatic cancer.

Indexed as

Biomarkers, TumorGastrointestinal NeoplasmsGenetic Predisposition to DiseasePolymorphism, Single NucleotideVascular Endothelial Growth Factor ACase-Control StudiesHumansPrognosisRisk FactorsBiomarkers, TumorVascular Endothelial Growth Factor AVEGFA protein, humanAngiogenesisGastrointestinal tract cancersGenetic associationMeta-analysisVEGF +405C/G polymorphism

Identifiers

PMID40542752
PMCPMC12374524

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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.