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Article type: Research Article
Authors: Zitt, Matthias | Untergasser, Gerold | Amberger, Albert | Moser, Patrizia | Stadlmann, Sylvia | Zitt, Marion | Müller, Hannes M. | Mühlmann, Gilbert | Perathoner, Alexander | Margreiter, Raimund; | Gunsilius, Eberhard | Öfner, Dietmar
Affiliations: Department of General and Transplant Surgery, Innsbruck Medical University, Austria | Laboratory of Tumor Biology & Angiogenesis, Department of Hematology and Oncology, Innsbruck Medical University, Austria | Tyrolean Cancer Research Institute, Innsbruck, Austria | Department of Pathology, Innsbruck Medical University, Austria | Department of Pathology, Basel University Hospital, Switzerland
Note: [] Corresponding author: Matthias Zitt, MD, Department of General and Transplant Surgery, Innsbruck Medical University, Anichstrasse 35, A-6020 Innsbruck, Austria. Tel.: +43 512 504 0; Fax: +43 512 504 28519; E-mail: [email protected]
Abstract: Gene expression of Dickkopf-3 (Dkk-3) has been shown to be upregulated in tumor endothelium of colorectal cancer (CRC). For the first time, we analyzed Dkk-3 protein expression in CRC and its potential as a marker for neoangiogenesis. We used tissue microarrays (TMAs) to investigate Dkk-3 in microvessels of 403 CRC samples, 318 appropriate adjacent non-cancerous samples and 127 normal colorectal samples. Of cancer samples with CD31-positive microvessels, 67.7% were positive for Dkk-3. Dkk-3 staining was demonstrated in endothelial cells of all microvessels in nearly all cases. Dkk-3-positive samples showed a higher mean microvessel count than did Dkk-3-negative samples (P=0.001). Dkk-3 expression increased with rising numbers of microvessels per sample (P<0.0001). In adjacent samples with CD31-positive microvessels, 56% were Dkk-3-positive in all microvessels. Similar to cancer samples, Dkk-3-positive adjacent samples had a higher mean microvessel count than did Dkk-3-negative samples (P<0.0001), and Dkk-3 expression also increased with rising numbers of microvessels (P<0.0001). All microvessels in normal mucosa samples were negative for Dkk-3. Dkk-3 can be considered a putative pro-angiogenic protein in neovascularization and may possibly be a marker for neoangiogenesis in CRC. Further investigations will elucidate whether Dkk-3 is a target structure for novel therapies.
Keywords: Dickkopf-3, neoangiogenesis, colorectal cancer, adjacent tissue, tissue microarrays
Journal: Disease Markers, vol. 24, no. 2, pp. 101-109, 2008
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