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Correlation of VEGF +405C/G Polymorphism with Gastrointestinal Tract Cancers Risk: An Updated Meta-Analysis
Sukhpreet Kaur Walia1, Vasudha Sambyal1, Kamlesh Guleria1
1Human Cytogenetics Laboratory, Department of Human Genetics, Guru Nanak Dev University, Amritsar 143005, Punjab, India.
The vascular endothelial growth factor (VEGF) +405C/G polymorphism may indicate risk for esophageal, colorectal, and pancreatic cancers. This meta-analysis clarifies inconsistent findings regarding its association with gastrointestinal cancer risk.
Area of Science:
- Genetics and Molecular Biology
- Oncology
- Cancer Epidemiology
Background:
- Vascular Endothelial Growth Factor (VEGF) functional polymorphisms influence angiogenesis and tumor development.
- Previous studies on the association between VEGF +405C/G polymorphism and gastrointestinal (GI) cancer risk yielded inconsistent results.
- A meta-analysis is needed to clarify the role of this polymorphism in GI cancer development.
Purpose of the Study:
- To conduct a comprehensive meta-analysis clarifying the association between the VEGF +405C/G polymorphism and the risk of developing gastrointestinal cancers.
- To evaluate the overall association and stratified analyses based on ethnicity and cancer type.
Main Methods:
- A systematic literature search was performed across PubMed, Google Scholar, Web of Science, and Science Direct.
- Data from 23 studies, including 5,656 cases and 6,319 controls, were extracted and analyzed using MetaGenyo software.
- Inclusion and exclusion criteria were applied to ensure the quality and relevance of the selected studies.
Main Results:
- Overall analysis and ethnicity-stratified analyses did not reveal a significant association between VEGF +405C/G polymorphism and overall GI cancer risk.
- Subgroup analysis indicated a significant association with increased risk for esophageal cancer under several genetic models.
- Specific models showed significant associations with decreased risk for esophageal cancer and altered risks for colorectal and pancreatic cancers.
Conclusions:
- The VEGF +405C/G polymorphism may serve as a potential biomarker for assessing individual cancer risk.
- The findings suggest a specific role for this polymorphism in the risk of developing esophageal, colorectal, and pancreatic cancers.
- This meta-analysis provides valuable insights into the complex relationship between VEGF genetic variations and GI cancer susceptibility.
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