| Literature DB >> 18623110 |
Frank A Orlando1, Dongfeng Tan, Juan D Baltodano, Thaer Khoury, John F Gibbs, Victor J Hassid, Bestoun H Ahmed, Sadir J Alrawi.
Abstract
Colorectal cancer progression originates when accumulated genetic and epigenetic alterations cause genomic instability and a malignant phenotype. Subsequent molecular pathway deregulation leads to histopathologic changes that are clinically evident as aberrant crypt foci (ACF) and visualized by high-magnification chromoscopic colonoscopy. ACF are biomarkers of increased colorectal cancer risk, particularly those with dysplastic features. Genetic profiling using genomic instability, loss of heterozygosity, and methylation analysis has revealed a minority population of ACF genotypically analogous to cancer.Entities:
Mesh:
Year: 2008 PMID: 18623110 PMCID: PMC3971525 DOI: 10.1002/jso.21106
Source DB: PubMed Journal: J Surg Oncol ISSN: 0022-4790 Impact factor: 3.454