| Literature DB >> 35821636 |
Zoe Raglow1, Mary Kathryn McKenna2, Challice L Bonifant3, Wenjing Wang4, Marina Pasca di Magliano5, Johannes Stadlmann6, Josef M Penninger7, Richard D Cummings8, Malcolm K Brenner9, David M Markovitz10.
Abstract
Chimeric antigen receptor (CAR) T cell therapy has created a paradigm shift in the treatment of hematologic malignancies but has not been as effective toward solid tumors. For such tumors, the primary obstacles facing CAR T cells are scarcity of tumor-specific antigens and the hostile and complex tumor microenvironment. Glycosylation, the process by which sugars are post-translationally added to proteins or lipids, is profoundly dysregulated in cancer. Abnormally glycosylated glycoproteins expressed on cancer cells offer unique targets for CAR T therapy as they are specific to tumor cells. Tumor stromal cells also express abnormal glycoproteins and thus also have the potential to be targeted by glycan-binding CAR T cells. This review will discuss the state of CAR T cells in the therapy of solid tumors, the cancer glycoproteome and its potential for use as a therapeutic target, and the landscape and future of glycan-binding CAR T cell therapy.Entities:
Keywords: CAR T cell therapy; cancer glycobiology; glycan; glycoprotein; solid tumor; tumor microenvironment
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Year: 2022 PMID: 35821636 PMCID: PMC9481985 DOI: 10.1016/j.ymthe.2022.07.006
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 12.910