| Literature DB >> 31948560 |
Jordan J Cardenas1, Camila Robles-Oteiza1, Katerina Politi2.
Abstract
Patient-derived xenografts are a useful tool in cancer immunology, as they allow researchers to study human cancers in vivo when starting with a relatively small amount of human tumor tissue. These models make it possible to study tumor cell-intrinsic changes that occur in response to external stimuli including cytokines like interferon gamma (IFNγ) that are important for effective anti-tumor immune responses. IFNγ responsiveness can be measured by assessing surface expression of MHC class I on tumor cells, the molecule on which tumor antigens are presented to cytotoxic T cells in the tumor microenvironment. Low levels of MHC class I and lack of responsiveness have been associated with resistance to T-cell directed therapies like immune checkpoint inhibitors. In this chapter, we present a protocol for an assay to screen patient-derived xenografts for their responsiveness to IFNγ. The results of this assay can be used as a starting point for uncovering cancer cell-intrinsic mechanisms of resistance to immunotherapies in patient tumors.Entities:
Keywords: Flow cytometry; Immunotherapy; Interferon gamma; MHC-I antigen presentation; Patient-derived xenograft
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Year: 2019 PMID: 31948560 PMCID: PMC7299176 DOI: 10.1016/bs.mie.2019.10.027
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600