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[Cancer Research 66, 3078-3086, March 15, 2006]
© 2006 American Association for Cancer Research


Cell, Tumor, and Stem Cell Biology

Behavioral Profiling of Human Transitional Cell Carcinoma Ex vivo

Carlos R. Estrada1,6, Matthew Salanga2, Diane R. Bielenberg3,6, W. Bruce Harrell1,6, David Zurakowski4,8, Xuping Zhu5,9, Matthew R. Palmer5,9, Michael R. Freeman1,6,7 and Rosalyn M. Adam1,6

1 Urological Diseases Research Center, 2 Department of Neurology Imaging Core, 3 Vascular Biology Program, 4 Department of Orthopaedics, Children's Hospital Boston; Departments of 5 Radiology, Beth Israel Deaconess Medical Center; Departments of 6 Surgery, 7 Biological Chemistry and Molecular Pharmacology, 8 Orthopaedic Surgery, and 9 Radiology, Harvard Medical School, Boston, Massachusetts

Requests for reprints: Rosalyn M. Adam, Enders Research Laboratories, Room 1077, 300 Longwood Avenue, Boston, MA 02115. Phone: 617-919-2019; Fax: 617-730-0248; E-mail: rosalyn.adam{at}childrens.harvard.edu.

Outcome studies of many types of cancer have revealed that tumors of indistinguishable histologic appearance may differ significantly in aggressiveness and in their response to therapy. A strategy that would enable early identification of patients at high risk for disease progression and allow screening of multiple therapeutic agents simultaneously for efficacy would improve clinical management. We have developed an orthotopic organ culture model of bladder cancer in which quantum dot–based fluorescent imaging approaches are used to obtain quantitative measurements of tumor cell behavior. Human transitional cell carcinoma (TCC) cells are labeled with quantum dot nanoparticles, and the cells instilled into the rat bladder in vivo, after which the bladder is excised and cultured ex vivo. Cell implantation, proliferation, and invasion into the organ wall are monitored using epifluorescence imaging and two-photon laser scanning confocal microscopy. Using this approach, we were able to assign distinct phenotypes to two metastatic bladder cancer cell lines based on different patterns of invasiveness into the bladder wall. We also showed that established tumor cell masses regressed following intravesical administration of the chemotherapeutic drug thiotepa. Collectively, these findings suggest that this assay system, which we have named EViTAS (for ex vivo tumor assay system), can recapitulate salient aspects of tumor growth in the host and is amenable to behavioral profiling of human cancer. (Cancer Res 2006; 66(6): 3078-86)







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
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Annual Meeting Education Book Meeting Abstracts Online
Copyright © 2006 by the American Association for Cancer Research.