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Cancer Research 69, 5357, July 1, 2009. Published Online First June 23, 2009;
doi: 10.1158/0008-5472.CAN-08-3895
© 2009 American Association for Cancer Research

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Cell, Tumor, and Stem Cell Biology

Nanoscale Cellular Changes in Field Carcinogenesis Detected by Partial Wave Spectroscopy

Hariharan Subramanian1, Hemant K. Roy2, Prabhakar Pradhan1, Michael J. Goldberg2, Joseph Muldoon2, Randall E. Brand2, Charles Sturgis2, Thomas Hensing2, Daniel Ray2, Andrej Bogojevic2, Jameel Mohammed2, Jeen-Soo Chang2 and Vadim Backman1

1 Biomedical Engineering Department, Northwestern University and 2 Department of Internal Medicine, Northshore University HealthSystem, Evanston, Illinois

Requests for reprints: Vadim Backman, 2145 Sheridan Road, E310, Evanston, IL 60208. Phone: 847-491-3536; Fax: 847-491-4928; E-mail: v-backman{at}northwestern.edu.

Key Words: field carcinogenesis • light scattering • disorder • nanoscale alterations • microscopy

Understanding alteration of cell morphology in disease has been hampered by the diffraction-limited resolution of optical microscopy (>200 nm). We recently developed an optical microscopy technique, partial wave spectroscopy (PWS), which is capable of quantifying statistical properties of cell structure at the nanoscale. Here we use PWS to show for the first time the increase in the disorder strength of the nanoscale architecture not only in tumor cells but also in the microscopically normal-appearing cells outside of the tumor. Although genetic and epigenetic alterations have been previously observed in the field of carcinogenesis, these cells were considered morphologically normal. Our data show organ-wide alteration in cell nanoarchitecture. This seems to be a general event in carcinogenesis, which is supported by our data in three types of cancer: colon, pancreatic, and lung. These results have important implications in that PWS can be used as a new method to identify patients harboring malignant or premalignant tumors by interrogating easily accessible tissue sites distant from the location of the lesion. [Cancer Res 2009;69(13):5357–63]







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Copyright © 2009 by the American Association for Cancer Research.