Abstract

Abstract One of the major hurdles for population screening for cancer is the low prevalence of disease (generally significantly less than 10%) in the target population. Devising an accurate, minimally-intrusive risk-stratification technique is therefore of paramount importance for efficacious population screening. Our group has developed a suite of light-scattering technologies that allow quantification of subtle micro/nanoscale architecture consequences of the well-established genetic/epigenetic alterations of field carcinogenesis. These occur in the microscopically normal mucosa as the particle sizes (e.g., ribosomes, mitochondria, macromolecular complexes) are below the diffraction limit of light (∼0.5 microns). We have used these techniques to interrogate easily accessible surrogate sites for cancer risk assessment. For instance, using a fiberoptic probe inserted into the rectum can sense the risk of advanced adenomas with ∼90% accuracy. Furthermore, buccal swabs have been shown to discriminate between smokers with and without lung cancer with excellent performance. This paradigm may exist for a number of cancer types (esophageal, ovarian, pancreas, etc.) thereby providing a broad platform for population prescreening. Citation Information: Cancer Prev Res 2010;3(12 Suppl):PL02-03.

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