| Literature DB >> 35246703 |
Liyan Qu1, Jiakang Jin2,3, Jianan Lou2,3, Chao Qian2,3, Jinti Lin2,3, Ankai Xu2,3, Bing Liu2,3, Man Zhang2,3, Huimin Tao4,5, Wei Yu6,7.
Abstract
As the main immune checkpoint, PD-L1-PD-1 interaction plays a critical role in the dysregulation of effector T cells, which contributes to the failure of Chimeric Antigen Receptor T-cell (CAR-T) and other immunotherapies. Presently, most research focuses on the extracellular function of PD-L1. Membrane PD-L1 can interact with its receptor PD-1 and decrease T cell-induced cancer immunity. However, the function of PD-L1 in cancer cells is still unclear. Recent studies have shown the separated clinical significance of PD-L1 expression in various cancer types, showing the complexity of PD-L1 in cancer cell regulation. As a novel regulatory pathway, the nuclear translocation of PD-L1 in cancer cells receives more attention. Results of these preclinical studies demonstrated that nuclear PD-L1 has an essential role in cancer development and other immune checkpoint molecules transcription. Herein, we summarized the mechanisms involved in PD-L1 nuclear transportation and identify the key regulatory factors in this process. Furthermore, we also summarize the function of nuclear PD-L1 in cancer immunity. These findings suggested the novel PD-L1 regulation in cancer development, which showed that nuclear PD-L1 is a potential therapeutic target in future cancer therapy.Entities:
Keywords: Cancer immunity and immunotherapy; Immune escape; Nuclear transportation; PD-L1; Transcriptional regulation
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Year: 2022 PMID: 35246703 DOI: 10.1007/s00262-022-03176-7
Source DB: PubMed Journal: Cancer Immunol Immunother ISSN: 0340-7004 Impact factor: 6.630