USP15: a review of its implication in immune and inflammatory processes and tumor progression
- PMID: 33824497
- DOI: 10.1038/s41435-021-00125-9
USP15: a review of its implication in immune and inflammatory processes and tumor progression
Abstract
The covalent post-translational modification of proteins by ubiquitination not only influences protein stability and half-life, but also several aspects of protein function including enzymatic activity, sub-cellular localization, and interactions with binding partners. Protein ubiquitination status is determined by the action of large families of ubiquitin ligases and deubiquitinases, whose combined activities regulate many physiological and cellular pathways. The Ubiquitin Specific Protease (USP) family is one of 8 subfamilies of deubiquitinating enzymes composed of more than 50 members. Recent studies have shown that USP15 plays a critical role in regulating many aspects of immune and inflammatory function of leukocytes in response to a broad range of infectious and autoimmune insults and following tissue damage. USP15 regulated pathways reviewed herein include TLR signaling, RIG-I signaling, NF-kB, and IRF3/IRF7-dependent transcription for production of pro-inflammatory cytokines and type I interferons. In addition, USP15 has been found to regulate pathways implicated in tumor onset and progression such as p53, and TGF-β signaling, but also influences the leukocytes-determined immune and inflammatory microenvironment of tumors to affect progression and outcome. Hereby reviewed are recent studies of USP15 in model cell lines in vitro, and in mutant mice in vivo with reference to available human clinical datasets.
Similar articles
-
Ubiquitin-specific Protease 15 Negatively Regulates Virus-induced Type I Interferon Signaling via Catalytically-dependent and -independent Mechanisms.Sci Rep. 2015 Jun 10;5:11220. doi: 10.1038/srep11220. Sci Rep. 2015. PMID: 26061460 Free PMC article.
-
The Multifaceted Roles of USP15 in Signal Transduction.Int J Mol Sci. 2021 Apr 29;22(9):4728. doi: 10.3390/ijms22094728. Int J Mol Sci. 2021. PMID: 33946990 Free PMC article. Review.
-
The Regulations of Deubiquitinase USP15 and Its Pathophysiological Mechanisms in Diseases.Int J Mol Sci. 2017 Feb 24;18(3):483. doi: 10.3390/ijms18030483. Int J Mol Sci. 2017. PMID: 28245560 Free PMC article. Review.
-
The ubiquitin-specific protease USP15 promotes RIG-I-mediated antiviral signaling by deubiquitylating TRIM25.Sci Signal. 2014 Jan 7;7(307):ra3. doi: 10.1126/scisignal.2004577. Sci Signal. 2014. PMID: 24399297 Free PMC article.
-
USP15 potentiates NF-κB activation by differentially stabilizing TAB2 and TAB3.FEBS J. 2020 Aug;287(15):3165-3183. doi: 10.1111/febs.15202. Epub 2020 Jan 19. FEBS J. 2020. PMID: 31903660
Cited by
-
Transcription Factors, R-Loops and Deubiquitinating Enzymes: Emerging Targets in Myelodysplastic Syndromes and Acute Myeloid Leukemia.Cancers (Basel). 2021 Jul 26;13(15):3753. doi: 10.3390/cancers13153753. Cancers (Basel). 2021. PMID: 34359655 Free PMC article. Review.
-
Genome-wide sequencing identifies a thermal-tolerance related synonymous mutation in the mussel, Mytilisepta virgata.Commun Biol. 2023 Jan 3;6(1):5. doi: 10.1038/s42003-022-04407-4. Commun Biol. 2023. PMID: 36596992 Free PMC article.
-
PRDM1 promotes the ferroptosis and immune escape of thyroid cancer by regulating USP15-mediated SELENBP1 deubiquitination.J Endocrinol Invest. 2024 Dec;47(12):2981-2997. doi: 10.1007/s40618-024-02385-4. Epub 2024 Jul 16. J Endocrinol Invest. 2024. PMID: 39014173
-
In vivo CRISPR screens reveal SCAF1 and USP15 as drivers of pancreatic cancer.Nat Commun. 2024 Jun 20;15(1):5266. doi: 10.1038/s41467-024-49450-3. Nat Commun. 2024. PMID: 38902237 Free PMC article.
-
A strategy for orthogonal deubiquitination using a bump-and-hole approach.RSC Chem Biol. 2023 Oct 2;4(11):879-883. doi: 10.1039/d3cb00095h. eCollection 2023 Nov 1. RSC Chem Biol. 2023. PMID: 37920396 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous