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CD36 rs1761667 Polymorphism and Its Impact on Molecular Signatures in Bladder Cancer.
Mihai Ioan Pavalean1,2, Ioana Maria Lambrescu1,3, Gisela Gaina1,3
1Department of Morphological Sciences, Carol Davila University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Genetic variations in CD36 may influence bladder cancer risk. The rs1761667 variant was linked to altered CD36 mRNA expression in bladder cancer patients, suggesting a potential role in disease pathways.
Area of Science:
- Genetics
- Oncology
- Molecular Biology
Background:
- Bladder cancer is a complex disease with emerging genetic links.
- CD36, a scavenger receptor, is involved in lipid metabolism and tumor progression.
- The role of CD36 genetic variants in bladder cancer is unexplored.
Purpose of the Study:
- To investigate the association between the rs1761667 single nucleotide polymorphism and CD36 mRNA expression levels.
- To explore the potential impact of CD36 genetic variation on bladder cancer pathogenesis.
Main Methods:
- Genotyping of the rs1761667 variant using PCR-RFLP in 30 bladder cancer patients and 19 controls.
- Quantification of CD36 mRNA expression via RT-qPCR.
- Statistical analysis of genotype-expression correlations using the 2-ΔΔCt method.
Main Results:
- CD36 mRNA expression significantly differed among rs1761667 genotypes in bladder cancer patients.
- AA genotype carriers exhibited reduced CD36 expression compared to GG carriers (p=0.03).
- No significant genotype-dependent expression differences were found in controls, and genotype distributions did not differ between cases and controls.
Conclusions:
- The rs1761667 variant may influence CD36 transcription in a genotype-dependent manner within the context of bladder cancer.
- These findings suggest a potential link between inherited CD36 variations and bladder cancer-related biological pathways.
- Further validation in tumor tissues is warranted to confirm these results.
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