Protocols and characterization data for 2D, 3D, and slice-based tumor models from the PREDECT project

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作者
Ronald de Hoogt
Marta F. Estrada
Suzana Vidic
Emma J. Davies
Annika Osswald
Michael Barbier
Vítor E. Santo
Kjersti Gjerde
Hanneke J. A. A. van Zoggel
Sami Blom
Meng Dong
Katja Närhi
Erwin Boghaert
Catarina Brito
Yolanda Chong
Wolfgang Sommergruber
Heiko van der Kuip
Wytske M. van Weerden
Emmy W. Verschuren
John Hickman
Ralph Graeser
机构
[1] Janssen Pharmaceutica N.V.,Department of Veterinary Sciences
[2] iBET,undefined
[3] Instituto de Biologia Experimental e Tecnológica,undefined
[4] Instituto de Tecnologia Química e Biológica António Xavier,undefined
[5] Universidade Nova de Lisboa,undefined
[6] Institute of Biochemistry,undefined
[7] Faculty of Medicine,undefined
[8] University of Ljubljana,undefined
[9] Oncology IMED,undefined
[10] Bioscience,undefined
[11] AstraZeneca,undefined
[12] Boehringer Ingelheim RCV,undefined
[13] GmbH & Co. KG,undefined
[14] Institute of Medical Genetics,undefined
[15] Medical University of Vienna,undefined
[16] University of Antwerp,undefined
[17] Laboratory of Cell Biology & Histology,undefined
[18] ERASMUS MC,undefined
[19] Institute for Molecular Medicine Finland (FIMM),undefined
[20] Dr Margarete Fischer-Bosch Institute of Clinical Pharmacology and University of Tuebingen,undefined
[21] AbbVie,undefined
[22] Institut de Recherches Servier c/o 126 boulevard Pereire,undefined
[23] Boehringer Ingelheim Pharma GmbH & Co. KG,undefined
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摘要
Two-dimensional (2D) culture of cancer cells in vitro does not recapitulate the three-dimensional (3D) architecture, heterogeneity and complexity of human tumors. More representative models are required that better reflect key aspects of tumor biology. These are essential studies of cancer biology and immunology as well as for target validation and drug discovery. The Innovative Medicines Initiative (IMI) consortium PREDECT (www.predect.eu) characterized in vitro models of three solid tumor types with the goal to capture elements of tumor complexity and heterogeneity. 2D culture and 3D mono- and stromal co-cultures of increasing complexity, and precision-cut tumor slice models were established. Robust protocols for the generation of these platforms are described. Tissue microarrays were prepared from all the models, permitting immunohistochemical analysis of individual cells, capturing heterogeneity. 3D cultures were also characterized using image analysis. Detailed step-by-step protocols, exemplary datasets from the 2D, 3D, and slice models, and refined analytical methods were established and are presented.
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