| Literature DB >> 35819633 |
Dan-Dan Shen1,2, Ya-Ping Bi2, Jing-Ru Pang2, Li-Juan Zhao2,3, Long-Fei Zhao2, Ya Gao2, Bo Wang2, Hui-Min Liu2, Ying Liu4, Ning Wang5, Yi-Chao Zheng6,7,8, Hong-Min Liu9,10.
Abstract
Cancer immunotherapy is a rapidly developing and effective method for the treatment of a variety of malignancies in recent years. As a significant immune checkpoint, programmed cell death 1 ligand 1 (PD-L1) and its receptor programmed cell death protein 1 (PD-1) play the most significant role in cancer immune escape and cancer immunotherapy. Though PD-L1 have become an important target for drug development and there have been various approved drugs and clinic trials targeting it, and various clinical response rate and adverse reactions prevent many patients from benefiting from it. In recent years, combination trials have become the main direction of PD-1/PD-L1 antibodies development. Here, we summarized PD-L1 biofunctions and key roles in various cancers along with the development of PD-L1 inhibitors. The regulators that are involved in controlling PD-L1 expression including post-translational modification, mRNA level regulation as well as degradation and exosome secretory pathway of PD-L1 were focused. This systematic summary may provide comprehensive understanding of different regulations on PD-L1 as well as a broad prospect for the search of the important regulator of PD-L1. The regulatory factors of PD-L1 can be potential targets for immunotherapy and increase strategies of immunotherapy in combination.Entities:
Keywords: Cancer immunotherapy; Degradation; PD-L1; Regulation mechanisms; Structure
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Year: 2022 PMID: 35819633 DOI: 10.1007/s00018-022-04431-x
Source DB: PubMed Journal: Cell Mol Life Sci ISSN: 1420-682X Impact factor: 9.207