| Literature DB >> 35294592 |
Mahmoud Mohammad Yaseen1, Nizar Mohammad Abuharfeil2, Homa Darmani2.
Abstract
Immune checkpoint proteins, such as programmed cell death receptor 1 (PD-1) and its ligand (PD-L1), play critical roles in the pathology of chronic inflammatory pathological conditions, particularly cancer. In addition, the activation of PD-1/PD-L1 pathway is involved in mediating resistance to certain anti-cancer chemo- and immuno-therapeutics. Unfortunately, targeting the PD-1/PD-L1 pathway by the available anti-PD-1/PD-L1 drugs can benefit only a small proportion of cancer patients. Thus, studying the factors that regulate the expression of these immune checkpoint proteins is of central importance in this context. Recent investigations have identified CMTM6 and, to a lesser extent, CMTM4, as master regulators of PD-L1 expression in various cancer cells. Understanding the mechanisms by which such proteins upregulate the expression of PD-L1 in tumor cells, and determining the potential regulators of CMTM6 expression in different types of cancers will accelerate the development of new therapeutic targets and/or lead to the enhancement of the currently available PD-1/PD-L1 blockade therapies.Entities:
Keywords: Circular RNAs (circRNAs); Endosomal degradation; Epithelial to mesenchymal transition (EMT) transcription factor SNAIL; Hu-antigen R (HuR) protein; Proteasomal degradation; WEE1 and ATM Kinases
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Year: 2022 PMID: 35294592 DOI: 10.1007/s00262-022-03171-y
Source DB: PubMed Journal: Cancer Immunol Immunother ISSN: 0340-7004 Impact factor: 6.630