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Methylation profile in penile carcinoma reveals unique signature relative to surround tissue and HPV status

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BMC Proceedings20137 (Suppl 2) :P30

  • Published:


  • Methylation Profile
  • Differential Methylation
  • Unique Signature
  • Important Public Health Problem
  • Genomic Workbench


Penile carcinoma (PeCa) is an important public health problem in poor and developing countries. Despite the unpredictable behavior and aggressive treatment, there are few data on molecular and epigenetic mechanisms reported in PeCa. The aim of this study was to identify epigenetic profile in tumors and surrounding tissue as well as to identify molecular markers in PeCa, according to the Papillomavirus (HPV) infection.

Patients and methods

Paired PeCa and surrounding tissue samples were collected from 16 patients. Twenty tumors were also included. Methylated (MethylMiner - Invitrogen) and unmethylated (digested with restriction enzyme McrBC) enriched sequences were hybridized in a 244K Human DNA Methylation Microarray platform (Agilent Technologies). This assay interrogates 27,627 expanded CpG islands and 5081 shore CpG island regions. Genomic Workbench Standard (v 5.0.14) and BRB softwares were used to analyze the data.


It was considered only probes with p value<0.001, FDR <0.05 and located inside or in the gene promoter. HPV positivity was detected in 43% of cases (Linear Array HPV Test Genotyping - Roche), mainly for 16 and 18 subtypes. Penile carcinoma displayed unique signature relative to surround tissue, showing 171 probes methylated and 349 unmethylated exclusively in tumor samples. Several probes related to genes involved in NOTCH and WNT pathways were altered in HPV positive cases.


It was found a differential methylation profile according to HPV status (positive or negative), indicating at least two disrupted pathways, one related to viral infection and the other associated with transcriptional regulation of stem cells.

Financial support


Authors’ Affiliations

Department of General Biology, Londrina State University, Londrina, PR, Brazil
CIPE - AC Camargo Cancer Hospital, São Paulo, SP, Brazil
Epigenetics Group, International Agency for Research on Cancer (IARC), Lyon, France
Institute of Biosciences, UNESP, Botucatu, SP, Brazil
Barretos Cancer Hospital, Barretos, SP, Brazil
Department of Pathology, UNICAMP, Campinas, SP, Brazil
Department of Urology, Faculty of Medicine, UNESP, Botucatu, SP, Brazil


© Kuasne et al; licensee BioMed Central Ltd. 2013

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.