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Human Microtumors Generated in 3D: Novel Tools for Integrated In Situ Studies of Cancer Immunotherapies
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 3698584
Author(s) Hambach, Lothar; Buser, Andreas; Vermeij, Marcel; Pouw, Nadine; van der Kwast, Theo; Goulmy, Els
Author(s) at UniBasel Buser, Andreas
Year 2016
Title Human Microtumors Generated in 3D: Novel Tools for Integrated In Situ Studies of Cancer Immunotherapies
Journal Methods in Molecular Biology
Volume 1393
Pages / Article-Number 147-61
Abstract Cellular immunotherapy targeting human tumor antigens is a promising strategy to treat solid tumors. Yet clinical results of cellular immunotherapy are disappointing. Moreover, the currently available in vitro human tumor models are not designed to study the optimization of T-cell therapies of solid tumors. Here, we describe a novel assay for multiparametric in situ analysis of therapeutic effects on individual human three-dimensional (3D) tumors. In this assay, tumors of several millimeter diameter are generated from human cancer cell lines of different tumor entities in a collagen type I microenvironment. A newly developed approach for efficient morphological analysis reveals that these in vitro tumors resemble many characteristics of the corresponding clinical cancers such as histological features, immunohistochemical staining patterns, distinct tumor growth compartments and heterogeneous protein expression. To assess the response to therapy with tumor antigen specific T-cells, standardized protocols are described to determine T-cell infiltration and tumor destruction by monitoring soluble factors and tumor growth. Human tumors engineered in 3D collagen scaffolds are excellent in vitro surrogates for avascular tumor stages allowing integrated analyses of the antitumor efficacy of cancer specific immunotherapy in situ.
Publisher Humana Press
ISSN/ISBN 1064-3745 ; 1940-6029
edoc-URL http://edoc.unibas.ch/52188/
Full Text on edoc No
Digital Object Identifier DOI 10.1007/978-1-4939-3338-9_15
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/27033225
ISI-Number WOS:000376532000016
Document type (ISI) Journal Article
 
   

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