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Issue title: 40th Conference of the German Society for Clinical Microcirculation and Hemorheology, 5-6 November 2021, Senftenberg, Germany
Guest editors: J.-H. Küpper, A. Krüger-Genge and F. Jung
Article type: Research Article
Authors: Kohl, Cynthiaa; * | Aung, Thihab; c | Haerteis, Silkeb | Papathemelis, Thomasa
Affiliations: [a] Department of Gynecology and Obstetrics, St. Marien Hospital Amberg, Amberg, Germany | [b] Institute for Molecular and Cellular Anatomy, University of Regensburg, Regensburg, Germany | [c] Center of Plastic, Aesthetic, Hand and Reconstructive Surgery, University of Regensburg, Regensburg, Germany
Correspondence: [*] Corresponding author: Dr. Cynthia Kohl, Department of Gynecology and Obstetrics, St. Marien Hospital Amberg, Amberg, Germany. Tel.: +49 9621 381371; Fax: +49 9621 381358; E-mail: kohlc001@klinikum-amberg.de.
Abstract: BACKGROUND:Breast cancer is the most common malignant tumor in women and highly heterogeneous with a variety of different molecular subtypes. The analysis of the individual tumor biology is necessary to develop a specific and individualized treatment plan for every patient. The chick chorioallantoic membrane (CAM) model, a 3D-in-vivo-tumor-model, could potentially provide a methodology that facilitates the gain of additional information regarding the tumor biology as well as the testing of the tumor’s individual sensitivity to different therapies. OBJECTIVE:The objective was to establish the grafting of different breast cancer primaries onto the CAM for tumor profiling and the investigation of different parameters. METHODS:Breast cancer primary tissue of different patients was grafted onto the CAM. Subsequently, 3D volume and perfusion measurements were performed during the engraftment period. Histological analyses of the tumors were carried out after the engraftment period. RESULTS:The grafting of the breast cancer primaries onto the CAM was successful. The tumors remained partially vital and displayed angiogenic development on the CAM. CONCLUSIONS:Breast cancer primary material can be grafted onto the CAM and we observed visible and measurable changes of perfusion over time.
Keywords: Breast cancer primary material, breast cancer, CAM model, 3D-in-vivo-tumor-model
DOI: 10.3233/CH-219113
Journal: Clinical Hemorheology and Microcirculation, vol. 79, no. 1, pp. 157-166, 2021
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