| Literature DB >> 25139296 |
Taku Harada1, Eiichiro Yamamoto2, Hiro-o Yamano3, Masanori Nojima4, Reo Maruyama2, Kohei Kumegawa5, Masami Ashida5, Kenjiro Yoshikawa3, Tomoaki Kimura3, Eiji Harada3, Ryo Takagi3, Yoshihito Tanaka3, Hironori Aoki6, Masayo Nishizono3, Michiko Nakaoka3, Akihiro Tsuyada5, Takeshi Niinuma2, Masahiro Kai5, Kazuya Shimoda7, Yasuhisa Shinomura8, Tamotsu Sugai9, Kohzoh Imai4, Hiromu Suzuki10.
Abstract
Aberrant DNA methylation could potentially serve as a biomarker for colorectal neoplasms. In this study, we assessed the feasibility of using DNA methylation detected in bowel lavage fluid (BLF) for colorectal cancer screening. A total of 508 BLF specimens were collected from patients with colorectal cancer (n = 56), advanced adenoma (n = 53), minor polyp (n = 209), and healthy individuals (n = 190) undergoing colonoscopy. Methylation of 15 genes (miR-1-1, miR-9-1, miR-9-3, miR-34b/c, miR-124-1, miR-124-2, miR-124-3, miR-137, SFRP1, SFRP2, APC, DKK2, WIF1, LOC386758, and ZNF582) was then analyzed in MethyLight assays, after which receiver operating characteristic (ROC) curves were analyzed to assess the diagnostic performance of BLF methylation. Through analyzing BLF specimens in a training set (n = 345), we selected the three genes showing the greatest sensitivity for colorectal cancer detection (miR-124-3, 71.8%; LOC386758, 79.5%; and SFRP1, 74.4%). A scoring system based on the methylation of those three genes (M-score) achieved 82% sensitivity and 79% specificity, and the area under the ROC curve (AUC) was 0.834. The strong performance of this system was then validated in an independent test set (n = 153; AUC = 0.808). No significant correlation was found between M-score and the clinicopathologic features of the colorectal cancers. Our results demonstrate that DNA methylation in BLF specimens may be a useful biomarker for the detection of colorectal cancer. ©2014 American Association for Cancer Research.Entities:
Mesh:
Substances:
Year: 2014 PMID: 25139296 DOI: 10.1158/1940-6207.CAPR-14-0162
Source DB: PubMed Journal: Cancer Prev Res (Phila) ISSN: 1940-6215