Volume 77, Issue 3 pp. 455-459
Experimental Cancer

Angiogenic potential of malignant and non-malignant human breast tissues in an in vivo angiogenesis model

Hera C. Lichtenbeld

Hera C. Lichtenbeld

Department of Internal Medicine, University Hospital Maastricht, Maastricht, The Netherlands

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Annemarie F. Barendsz-Janson

Annemarie F. Barendsz-Janson

Department of Internal Medicine, University Hospital Maastricht, Maastricht, The Netherlands

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Helma van Essen

Helma van Essen

Department of Internal Medicine, University Hospital Maastricht, Maastricht, The Netherlands

Department of Pharmacology, University of Maastricht, Maastricht, The Netherlands

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Harry Struijker Boudier

Harry Struijker Boudier

Department of Pharmacology, University of Maastricht, Maastricht, The Netherlands

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Arjan W. Griffioen

Arjan W. Griffioen

Department of Internal Medicine, University Hospital Maastricht, Maastricht, The Netherlands

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Harry F. P. Hillen

Corresponding Author

Harry F. P. Hillen

Department of Internal Medicine, University Hospital Maastricht, Maastricht, The Netherlands

Department of Internal Medicine, Academic Hospital Maastricht, P.O. Box 5800, 6202 AZ Maastricht, The Netherlands. Fax: (31) 43-387-5006Search for more papers by this author

Abstract

Tumors need to acquire an angiogenic phenotype for outgrowth and metastasis formation. Limited information on the angiogenic potential of specific tissues, especially human breast tissues is available. Here we describe an in vivo model, using the dorsal skin fold chamber in immunodeficient nude mice, where various tissues of human breast origin were xenografted and evaluated for their angiogenesis-inducing potential. We found that angiogenesis was abundantly induced by all breast carcinoma tissue samples. Similar angiogenesis was induced by tissue samples from breasts with hyperplasia and apocrine metaplasia. Histologically normal tissues adjacent to the tumor induced angiogenesis in 66% of the cases. Angiogenesis was not induced by control tissues from normal healthy breasts, obtained after cosmetic breast reduction. Angiogenesis induction parallelled VEGF production by the tumor cells. The tissue induced neovascularization, found both around and in the human tissue, was functional since a tail vein injection of albumin-FITC revealed positive tumor microcirculation within 5 min, while the tumor tissue still consisted of vital human epithelial cells after 14 days. Int. J. Cancer 77:455–459, 1998. © 1998 Wiley-Liss, Inc.

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