Year: 2019
Type: article
Study design: Observational Study
Abstract: A major challenge for the reduction of colon cancer is to detect patients carrying high-risk premalignant adenomas with minimally invasive testing. As one step, we have addressed the feasibility of detecting protein signals in the serum of patients carrying an adenoma as small as 6-9 mm in maximum linear dimension. Serum protein biomarkers, discovered in two animal models of early colonic adenomagenesis, were studied in patients using quantitative mass-spectrometric assays. One cohort included patients bearing adenomas known to be growing on the basis of longitudinal computed tomographic colonography. The other cohort, screened by optical colonoscopy, included both patients free of adenomas and patients bearing adenomas whose risk status was judged by histopathology. The markers F5, ITIH4, LRG1, and VTN were each elevated both in this patient study and in the studies of the Pirc rat model. The quantitative study in the Pirc rat model had demonstrated that the elevated level of each of these markers is correlated with the number of colonic adenomas. However, the levels of these markers in patients were not significantly correlated with the total adenoma volume. Postpolypectomy blood samples demonstrated that the elevated levels of these four conserved markers persisted after polypectomy. Two additional serum markers rapidly renormalized after polypectomy: growth-associated CRP levels were enhanced only with high-risk adenomas, while PI16 levels, not associated with growth, were reduced regardless of risk status. We discuss biological hypotheses to account for these observations, and ways for these signals to contribute to the prevention of colon cancer.
Language: English
Subfield: Oncology
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Funders: Wisconsin Alumni Research Foundation, University of Wisconsin-Madison, University of Wisconsin Carbone Cancer Center, National Institutes of Health, School of Medicine and Public Health, University of Wisconsin-Madison, National Cancer Institute, National Institute of General Medical Sciences, National Institute of Environmental Health Sciences, National Center for Advancing Translational Sciences
Awards: G1712026730, G2584911113, G4004214011, Biotechnology Training Program, Analyses of Progression to Colon Cancer in a Spectrum of Pathways, G5813506420, Molecular and Cellular Mechanisms of Tumor Development, G6291298690, Virtual Colonoscopy and Colorectal Cancer Screening, Ultra-Low Radiation Dose Body CT Imaging, G7092232967, G761346317, Comparative Effectiveness of Virtual and Optical Colonoscopy for CRC Surveillance, GENES CONTROLLING NEOPLASIA OF THE INTESTINAL EPITHELIUM, The Role of Aryl Hyrocarbon Receptor in Colon Tumorigenesis, G9000213383, G9000352744, University of Wisconsin Institute for Clinical and Translational Research, UW Comprehensive Cancer Center Support
OpenAlex ID: W2940139661
