Research Paper
Novel surface targets and serum biomarkers from the ovarian cancer vasculature
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Volume 12, Issue 3 August 1, 2011
Pages 169 - 180
http://dx.doi.org/10.4161/cbt.12.3.16260
Authors: Dimitra Sasaroli, Phyllis A. Gimotty, Harsh B. Pathak, Rachel Hammond, Eleni Kougioumtzidou, Dionyssios Katsaros, Ron Buckanovich, Karthik Devarajan, Raphael Sandaltzopoulos, Andrew K. Godwin, Nathalie Scholler and George Coukos
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- Dimitra Sasaroli
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University of Pennsylvania, Philadelphia, PA USA; Democritus University of Thrace, Alexandroupolis, Greece
- Phyllis A. Gimotty
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University of Pennsylvania, Philadelphia, PA, USA
- Harsh B. Pathak
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Fox Chase Cancer Center, Philadelphia, PA, USA
- Rachel Hammond
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University of Pennsylvania, Philadelphia, PA, USA
- Eleni Kougioumtzidou
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University of Pennsylvania, Philadelphia, PA USA; Democritus University of Thrace, Alexandroupolis, Greece
- Dionyssios Katsaros
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University of Turin, Torino, Italy
- Ron Buckanovich
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University of Pennsylvania, Philadelphia, PA USA; University of Michigan, Ann Arbor, MI, USA
- Karthik Devarajan
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Fox Chase Cancer Center, Philadelphia, PA, USA
- Raphael Sandaltzopoulos
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Democritus University of Thrace, Alexandroupolis, Greece
- Andrew K. Godwin
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Fox Chase Cancer Center, Philadelphia, PA, USA
- Nathalie Scholler
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University of Pennsylvania, Philadelphia, PA USA
- George Coukos
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Corresponding author: gcks@mail.med.upenn.edu
University of Pennsylvania, Philadelphia, PA USA
Abstract:
The molecular phenotype of tumor vasculature is different from normal vasculature, offering new opportunities for diagnosis and therapy of cancer, but the identification of tumor-restricted targets remains a challenge. We investigated 13 tumor vascular markers (TVMs) from 50 candidates identified through expression profiling of ovarian cancer vascular cells and selected to be either transmembrane or secreted, and to be either absent or expressed at low levels in normal tissues while overexpressed in tumors, based on analysis of 1,110 normal and tumor tissues from publicly available Affymetrix microarray data. Tumor-specific expression of each TVM was confirmed at the protein level in tumor tissue and/or in serum. Among the 13 TVMs, 11 were expressed on tumor vascular endothelium; the remaining 2 TVMs were expressed by tumor leukocytes. Our results demonstrate that certain transmembrane TVMs such as ADAM12 and CDCP1 are selectively expressed in tumor vasculature and represent promising targets for vascular imaging or anti-vascular therapy of epithelial ovarian cancer, while secreted or shed molecules such as TNFRSF21/DR6 can function as serum biomarkers. We have identified novel tumor-specific vasculature markers which appear promising for cancer serum diagnostics, molecular imaging and/or therapeutic targeting applications and warrant further clinical development.
Received: May 2, 2011
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