| Literature DB >> 21779143 |
Matthew R Hughes1, Emina H Huang.
Abstract
Advances in molecular biology have defined the molecular basis for colorectal cancer (CRC). Though only a fraction of CRC has been determined to have a hereditary component, the discovery of genetic alterations in these clinical syndromes has permitted definition of similar discoveries in sporadic CRC. Here we will delineate the molecular basis for the most common of these defined syndromes, including familial adenomatous polyposis, hereditary non-polyposis colon cancer, MUTYH associated polyposis, Juvenile polyposis, Peutz-Jeghers syndrome, and Cowden's syndrome. The newest paradigm with implications for the pathogenesis of sporadic CRC is called the cancer stem cell hypothesis. As this paradigm also implicates aberrations in molecular pathways, a brief discussion of this hypothesis is included.Entities:
Year: 2011 PMID: 21779143 PMCID: PMC3138675 DOI: 10.1053/j.scrs.2010.12.002
Source DB: PubMed Journal: Semin Colon Rectal Surg ISSN: 1043-1489