| Literature DB >> 19435926 |
Sabine C Glöckner1, Mashaal Dhir, Joo Mi Yi, Kelly E McGarvey, Leander Van Neste, Joost Louwagie, Timothy A Chan, Wolfram Kleeberger, Adriaan P de Bruïne, Kim M Smits, Carolina A J Khalid-de Bakker, Daisy M A E Jonkers, Reinhold W Stockbrügger, Gerrit A Meijer, Frank A Oort, Christine Iacobuzio-Donahue, Katja Bierau, James G Herman, Stephen B Baylin, Manon Van Engeland, Kornel E Schuebel, Nita Ahuja.
Abstract
We have used a gene expression array-based strategy to identify the methylation of tissue factor pathway inhibitor 2 (TFPI2), a potential tumor suppressor gene, as a frequent event in human colorectal cancers (CRC). TFPI2 belongs to the recently described group of embryonic cell Polycomb group (PcG)-marked genes that may be predisposed to aberrant DNA methylation in early stages of colorectal carcinogenesis. Aberrant methylation of TFPI2 was detected in almost all CRC adenomas (97%, n = 56) and stages I to IV CRCs (99%, n = 115). We further explored the potential of TFPI2 as a biomarker for the early detection of CRC using stool DNA-based assays in patients with nonmetastatic CRC and average-risk noncancer controls who were candidates for screening. TFPI2 methylation was detected in stool DNA from stage I to III CRC patients with a sensitivity of 76% to 89% and a specificity of 79% to 93%. Detection of TFPI2 methylation in stool DNA may act as a useful adjunct to the noninvasive strategies for screening of CRCs in the future.Entities:
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Year: 2009 PMID: 19435926 PMCID: PMC3062162 DOI: 10.1158/0008-5472.CAN-08-0142
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701