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PMID: 17636483 Published · ppublish English Journal Article

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

Diagnostic cytopathology ·Vol. 35 ·No. 8 ·2007-08-00 ·Pages 498-502

Pu RT, Sheng ZM, Michael CW, Rhode MG, Clark DP, O'Leary TJ

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 RARbeta2, 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 (RARbeta2: 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.

MeSH Terms
DNA Methylation DNA, Neoplasm/genetics Epithelium/pathology Female Humans Male Mesothelioma/diagnosis,genetics Middle Aged Pilot Projects Reverse Transcriptase Polymerase Chain Reaction/methods
Chemicals
DNA, Neoplasm
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Pu Robert T
Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan 48109, USA. robertpu@umich.edu
Sheng Zong-Mei
Michael Claire W
Rhode Michael G
Clark Douglas P
O'Leary Timothy J
Article Info
Journal
Diagnostic cytopathology
Abbr.
Diagn Cytopathol
ISSN
8755-1039
Published
2007-08-00
Pages
498-502
Language
English
Region
United States
NLM ID
8506895
Subset
IM
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