Methylation profiling of mesothelioma using real-time methylation-specific PCR: A pilot study

Robert T. Pu, Zong Mei Sheng, Claire W. Michael, Michael G. Rhode, Douglas P. Clark, Timothy J. O'Leary

Research output: Contribution to journalArticlepeer-review

Abstract

We tested whether methylation profiles generated by real-time methylation-specific PCR (MSP) can be useful in differentiating benign, reactive mesothelial cell proliferation (RM) from malignant mesothelioma (MM). Forty-two of the 63 cases (67%) yielded informative results for RARβ2, GPC3, CDKN2A (p16), TERT, and CCND2 (cyclinD2) gene methylation. DNA methylation of any gene was observed in much higher frequency in MM cases than RM cases (63% vs. 33%, P < 0.05). Individual gene methylation was higher in the MM than the RM cases for most of the genes; however, this was not statistically significant (RARβ2: 58% vs. 33%, P > 0.05; GPC3: 36% vs. 27%, P > 0.05; CDKN2A: 4% vs. 0%; TERT: 4% vs. 0%), while CCND2 methylation was not detected in any case. Although preliminary, we demonstrate that real-time MSP can be applied to archival specimens and gene methylation profiling may have potential to be a useful ancillary tool to help distinguish MM from RM.

Original languageEnglish (US)
Pages (from-to)498-502
Number of pages5
JournalDiagnostic cytopathology
Volume35
Issue number8
DOIs
StatePublished - Aug 2007

Keywords

  • Gene methylatio profiling
  • Mesothelioma
  • Real-time MSP

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Histology

Fingerprint Dive into the research topics of 'Methylation profiling of mesothelioma using real-time methylation-specific PCR: A pilot study'. Together they form a unique fingerprint.

Cite this