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Methylation profiling of mesothelioma using real‐time methylation‐specific PCR: A pilot study
Author(s) -
Pu Robert T.,
Sheng ZongMei,
Michael Claire W.,
Rhode Michael G.,
Clark Douglas P.,
O'Leary Timothy J.
Publication year - 2007
Publication title -
diagnostic cytopathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.417
H-Index - 65
eISSN - 1097-0339
pISSN - 8755-1039
DOI - 10.1002/dc.20692
Subject(s) - methylation , cdkn2a , dna methylation , mesothelioma , microbiology and biotechnology , cdkn2b , cancer research , medicine , gene , biology , pathology , gene expression , genetics
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 . Diagn. Cytopathol. 2007;35:498–502. © 2007 Wiley‐Liss, Inc.