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DOI 10.1007/s11033-026-12776-w

Медицинская библиотека · Molecular biology reports · 2026

Integrated analysis of VEGFA rs833061 (- 460T > C) promoter polymorphism and serum YKL-40 levels in bladder cancer: evidence of a genotype-phenotype association.

Kaushik Rohit, Pawar Devender, Sharma Anuradha, Siwach Kiran, Rohilla Gulshan, Narwal Sonia, Khatri Nisha, Arora Ankit, Vashist Minakshi

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Аннотация

BACKGROUND

Angiogenesis plays a central role in bladder cancer progression. VEGFA regulates angiogenesis, whereas YKL-40 is a pro-angiogenic biomarker. The relationship between VEGFA polymorphism and circulating YKL-40 remains unclear.

METHODS AND

RESULTS

A hospital-based case-control study involving 120 bladder cancer patients and 120 age- and sex-matched healthy controls was conducted. VEGFA rs833061 genotyping was performed using ARMS-PCR and confirmed by Sanger sequencing. Serum YKL-40 concentrations were measured by ELISA. Multivariable binary logistic regression analysis adjusted for age, sex, and smoking status demonstrated that the CT and TT genotypes remained independently associated with an increased risk of bladder cancer. Serum YKL-40 concentrations were significantly elevated in patients and increased progressively with tumor stage. TT genotype carriers exhibited the highest serum YKL-40 levels.

CONCLUSIONS

After adjustment for age, sex, and smoking status, the VEGFA rs833061 polymorphism remained independently associated with bladder cancer susceptibility and circulating YKL-40 concentrations. These findings provide preliminary evidence of a genotype-phenotype relationship; however, validation in larger multicentre cohorts is required.

Для цитирования: Kaushik Rohit, Pawar Devender, Sharma Anuradha, Siwach Kiran, Rohilla Gulshan, Narwal Sonia, Khatri Nisha, Arora Ankit, Vashist Minakshi. Integrated analysis of VEGFA rs833061 (- 460T > C) promoter polymorphism and serum YKL-40 levels in bladder cancer: evidence of a genotype-phenotype association.. Molecular biology reports. 2026. DOI: 10.1007/s11033-026-12776-w.

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