| Literature DB >> 30442814 |
Jung-Mao Hsu1, Chia-Wei Li1, Yun-Ju Lai2, Mien-Chie Hung3,4.
Abstract
Posttranslational modifications (PTM) of PD-L1 have emerged as important regulatory mechanisms that modulate immunosuppression in patients with cancer. In exposure to inflammatory cytokines, cancer cells and antigen-presenting cells, such as macrophages and dendritic cells, express PD-L1 to inhibit the activity of effector T cells through PD-1 engagement. Recent studies suggested that glycosylation, phosphorylation, ubiquitination, sumoylation, and acetylation play important roles in the regulation of PD-L1 protein stability and translocation and protein-protein interactions. Aberrant alterations of PTMs directly influence PD-L1-mediated immune resistance. On the basis of the newly identified regulatory signaling pathways of PD-L1 PTMs, researchers have investigated the cancer therapeutic potential of natural food compounds, small-molecule inhibitors, and mAbs by targeting PD-L1 PTMs. Results of these preclinical studies demonstrated that targeting PTMs of PD-L1 yields promising antitumor effects and that clinical translation of these therapeutic strategies is warranted. Cancer Res; 78(22); 6349-53. ©2018 AACR. ©2018 American Association for Cancer Research.Entities:
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Year: 2018 PMID: 30442814 PMCID: PMC6242346 DOI: 10.1158/0008-5472.CAN-18-1892
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701