Evidence map›Paper›PMID 39382410›Full record

ArticleThe Indian journal of medical research2024

Association of VEGFA polymorphisms with the risk of oesophageal cancer in Punjab, India: A case-control study.

Kamlesh Guleria, Vasudha Sambyal, Sukhpreet Kaur Walia, Meena Sudan, Manjit Singh Uppal

Abstract read
In one paragraph

Article in The Indian journal of medical research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

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1citing papers in PubMed, 1 pooled it
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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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Kamlesh GuleriaDepartment of Human Genetics, Guru Nanak Dev University, Amritsar, Punjab, India.
Vasudha SambyalDepartment of Human Genetics, Guru Nanak Dev University, Amritsar, Punjab, India.
Sukhpreet Kaur WaliaDepartment of Human Genetics, Guru Nanak Dev University, Amritsar, Punjab, India.
Meena SudanDepartment of Radiation Oncology, Sri Guru Ram Das Institute of Medical Sciences and Research, Amritsar, Punjab, India.
Manjit Singh UppalDepartment of Surgery, Sri Guru Ram Das Institute of Medical Sciences and Research, Amritsar, Punjab, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & objectives Vascular endothelial growth factor (VEGF) is one of the most important angiogenic factors which stimulates tumour progression induction of endothelial cell migration and division, inhibition of the apoptosis of endothelial cells, induction of serine protease activity and enhancement of vascular permeability. This study aimed to investigate the correlation of VEGF+405G/C,-7C/T and+936C/T polymorphisms with oesophageal cancer risk. Methods DNA samples of 464 subjects (231 sporadic oesophageal cancer affected individuals and 233 controls) were genotyped forVEGF+936C/T,+405G/C and-7C/T polymorphisms. VEGF+936C/T and +405G/C polymorphisms were genotyped by PCR-RFLP method whereas VEGF-7C/T polymorphism was genotyped using Amplification refractory mutation system-polymerase chain reaction (ARMS-PCR). Results CT genotype of VEGF-7C/T polymorphism was significantly associated with reduced risk of oesophageal cancer. VEGF-7C/T polymorphism was significantly associated with reduced risk of oesophageal cancer underdominant, co-dominant, over dominant and log-additive genetic models in total patients and in the female group. C+936G+405T-7 haplotype was significantly associated with decreased risk (P=0.01)of oesophageal cancer in total patients and also in the male group (P=0.02). Interpretation & conclusions In future, replication of the findings of the present study in a larger sample from different ethnic groups, along with functional analysis, may be insightful for the role of VEGFA polymorphisms in the pathogenesis of oesophageal cancer. Identification of the correlation of VEGF variants with specific therapy in oesophageal cancer may help in better selection of patients and monitoring treatment response in VEGF-therapy.

Indexed as

Esophageal NeoplasmsGenetic Predisposition to DiseaseHaplotypesPolymorphism, Single NucleotideVascular Endothelial Growth Factor AAdultAgedCase-Control StudiesFemaleGenetic Association StudiesGenotypeHumansIndiaMaleMiddle AgedRisk FactorsVascular Endothelial Growth Factor AVEGFA protein, humanAngiogenesisoesophageal cancerpolymorphismuntranslated regionsVEGF

Identifiers

PMID39382410
PMCPMC11463243

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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.