Korean J Pathol.  2010 Dec;44(6):623-630.

Prognostic Significance of Methylation Profiles in Urothelial Carcinomas of the Bladder

Affiliations
  • 1Departmentsof Pathology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. bijou@skku.edu, kkmkys@skku.edu
  • 2Department of Urology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Abstract

BACKGROUND
Study on epigenetics of urothelial carcinomas has expanded and allowed better understanding of their correlation with clinicopathologic features. The aim of this study was to determine reliable predictive epigenetic markers for patients with urothelial carcinoma of urinary bladder.
METHODS
In 64 urothelial carcinomas of the urinary bladder, methylationspecific polymerase chain reaction with RAS association domain family 1A (RASSF1A), adenomatous polyposis coli (APC), death-associated protein-kinase (DAPK), runt-related transcription factor 3 (RUNX3), p14, p16 and MGMT was performed and correlated the results with p53 mutations, DNA ploidy, clinicopathologic parameters and recurrences.
RESULTS
Hypermethyation of RASSF1A, APC, DAPK, RUNX3, p14, p16 and MGMT promoters was observed in 35 (54.7%), 29 (45.3%), 18 (28.1%), 18 (28.1%), 9 (14.1%), 2 (3.1%), and 6 (9.4%) cases, respectively. Hypermethylation of RUNX3 and APC was significantly associated with high histologic grades and aneuploidy. Methylation of DAPK was significantly associated with muscle invasion. Methylation of DAPK and RUNX3 genes was significantly associated with recurrence. In survival analyses, methylation of RUNX3 gene and methylation-high (methylation at two or more loci) phenotype was significantly associated with poor recurrence-free survival.
CONCLUSIONS
Methylation of RUNX3 gene and methylation-high phenotype are significant indicator of recurrence.

Keyword

Methylation; Urothelial carcinoma; Genes, tumor suppressor; Prognosis

MeSH Terms

Adenomatous Polyposis Coli
Aneuploidy
DNA
Epigenomics
Genes, Tumor Suppressor
Humans
Methylation
Muscles
Phenotype
Ploidies
Polymerase Chain Reaction
Prognosis
Recurrence
Transcription Factor 3
Urinary Bladder
DNA
Transcription Factor 3
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