Investigating neoplastic progression of ulcerative colitis with label-free comparative proteomics.
Ontology highlight
ABSTRACT: Patients with extensive ulcerative colitis (UC) have an increased risk of colorectal cancer. Although UC patients generally undergo lifelong colonoscopic surveillance to detect dysplasia or cancer in the colon, detection of cancer in this manner is expensive and invasive. An objective biomarker of dysplasia would vastly improve the clinical management of cancer risk in UC patients. In the current study, accurate mass and time methods with ion intensity-based label-free proteomics are applied to profile individual rectal and colon samples from UC patients with dysplasia or cancer (UC progressors) compared to rectal samples from patients that are dysplasia/cancer free (UC nonprogressors) to identify a set of proteins in the rectum mucosa that differentiate the two groups. In addition to the
SUBMITTER: May D
PROVIDER: S-EPMC3017661 | biostudies-literature | 2011 Jan
REPOSITORIES: biostudies-literature
ACCESS DATA