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  • Meeting abstract
  • Open Access

The A148T variant of CDKN2A gene in bladder cancer

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Hereditary Cancer in Clinical Practice20119 (Suppl 2) :A11

  • Published:


  • Bladder Cancer
  • Urinary Bladder
  • Tumor Grade
  • Genetic Alteration
  • Polymorphic Variant


Cancer of the urinary bladder is a common malignant disease in Poland. Molecular genetic alterations play a key role in bladder cancer carcinogenesis. Understanding genetic events that lead to initiation and progression of bladder cancer remains an important challenge in urological research.

Materials and methods

44 lesions were determined to be non-invasive tumors (pTa), whereas 36 tumors were invasive (pT1-T4). Tumor grade was noted low (G1) in 46 cases and high (G2-3) in 34 cases. DNA samples were evaluated for CDKN2A mutations with the use of MSSCP and sequencing method.


We found common polymorphic variants reported in the literature at codon 148 in exon 2 (Arg148Thr) and at nucleotides 500 and 540 in the 3’untranslated region which were not considered to be functional variants. We compared the obtained frequencies for the particular CDKN2A variants with the control group for the Polish population examined by Debniak and colleagues (Cancer Research 2005) and we found a significant difference in A148T polymorphism occurrence in the group of the bladder cancer patients (G test, table 2 ×2: NBLADDER CANCER =80, NCONTROL=1210, G=10.214, p<0.01). The Nt 500c>g, Nt540c>t polymorphisms recorded in the group of the bladder cancer patients in our study is not different from those recorded in the control group.


The A148T variant of CDKN2A gene seems to be associated with an increased risk of bladder cancer development.

Authors’ Affiliations

Chair of Clinical and Laboratory Genetics, Medical University of Łodz, Poland
2nd Clinic of Urology Medical University of Łodz, Poland
Department of Ecology and Vertebrate Zoology, University of Łodz, Poland
Department of Urology, John Paul II Regional Hospital Belchatow, Poland


© Borkowska et al; licensee BioMed Central Ltd. 2011

This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.