Premium
Genetic variability in 13q33 and 9q34 is linked to aggressiveness patterns and a higher risk of progression of non‐muscle‐invasive bladder cancer at the time of diagnosis
Author(s) -
Lenfant Louis,
CancelTassin Geraldine,
Gazut Stéphane,
Compérat Eva,
Rouprêt Morgan,
Cussenot Olivier
Publication year - 2021
Publication title -
bju international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.773
H-Index - 148
eISSN - 1464-410X
pISSN - 1464-4096
DOI - 10.1111/bju.15254
Subject(s) - bladder cancer , single nucleotide polymorphism , genotyping , medicine , genome wide association study , cohort , interquartile range , oncology , genotype , snp , allele , cancer , biology , genetics , gene
Objective To identify single nucleotide polymorphisms (SNPs) associated with patterns of aggressiveness of non‐muscle‐invasive bladder cancer (NMIBC). Patients and Methods From January 2011 to December 2018, 476 patients with NMIBC were prospectively included. The first step aimed to identify SNPs associated with aggressiveness patterns (e.g. ≥pT1or high‐grade/Grade 3 or presence of carcinoma in situ ) by analysing the data of a genome‐wide association study (GWAS) on 165 patients with BC. The second step aimed to validate the SNPs previously identified, by genotyping the germline DNA of 311 patients with NMIBC. Results Overall, the median (interquartile range) age was 66 (58–75) years and the rate of patients with aggressive NMIBC was comparable between both groups (46% vs 46%, P = 1). GWAS data analysis identified four SNPs associated with an aggressive NMIBC (rs12615669, rs4976845, rs2989734, and rs2802288). In the validation cohort, the genotype CC of rs12615669, as well as age >70 years at the time of diagnosis were associated with aggressive NMIBC ( P = 0.008 and P < 0.001, respectively). Genotyping of the entire cohort showed an association between aggressive NMIBC and the T allele of rs12615669 ( P = 0.0007), the A allele of rs4976845 ( P = 0.012), and the A allele of rs2989734 ( P = 0.007). A significant association was also found for the entire cohort between the risk of progression and the A allele of rs4976845 ( P = 0.04). Conclusion This two‐phase study identified three SNPs (rs12615669, rs4976845, and rs2989734) associated with aggressive NMIBC and one SNP (rs4976845) associated with a higher risk of progression.