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Originally published online as doi:10.2353/ajpath.2008.070625 on January 17, 2008

Published online before print January 17, 2008
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(American Journal of Pathology. 2008;172:358-366.)
© 2008 American Society for Investigative Pathology
DOI: 10.2353/ajpath.2008.070625

Intratumoral Heterogeneity for Expression of Tyrosine Kinase Growth Factor Receptors in Human Colon Cancer Surgical Specimens and Orthotopic Tumors

Toshio Kuwai*, Toru Nakamura*, Sun-Jin Kim*, Takamitsu Sasaki*, Yasuhiko Kitadai*, Robert R. Langley*, Dominic Fan*, Stanley R. Hamilton{dagger} and Isaiah J. Fidler*

From the Departments of Cancer Biology*and Pathology,{dagger}The University of Texas M. D. Anderson Cancer Center, Houston, Texas

The design of targeted therapy, particularly patient-specific targeted therapy, requires knowledge of the presence and intratumoral distribution of tyrosine kinase receptors. To determine whether the expression of such receptors is constant or varies between and within individual colon cancer neoplasms, we examined the pattern of expression of the ligands, epidermal growth factor, vascular endothelial growth factor, and platelet-derived growth factor-B as well as their respective receptors in human colon cancer surgical specimens and orthotopic human colon cancers growing in the cecal wall of nude mice. The expression of the epidermal growth factor receptor and the vascular endothelial growth factor receptor on tumor cells and stromal cells, including tumor-associated endothelial cells, was heterogeneous in surgical specimens and orthotopic tumors. In some tumors, the receptor was expressed on both tumor cells and stromal cells, and in other tumors the receptor was expressed only on tumor cells or only on stromal cells. In contrast, the platelet-derived growth factor receptor was expressed only on stromal cells in both surgical specimens and orthotopic tumors. Examination of receptor expression in both individual surgical specimens and orthotopic tumors revealed that the platelet-derived growth factor receptor was expressed only on stromal cells and that the patterns of epidermal growth factor receptor and vascular endothelial growth factor receptor 2 expression differed between tumor cells. This heterogeneity in receptor expression among different tumor cells suggests that targeting a single tyrosine kinase may not yield eradication of the disease.








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