An inhibitor of NEDD8-activating enzyme as a new approach to treat cancer
- PMID: 19360080
- DOI: 10.1038/nature07884
An inhibitor of NEDD8-activating enzyme as a new approach to treat cancer
Abstract
The clinical development of an inhibitor of cellular proteasome function suggests that compounds targeting other components of the ubiquitin-proteasome system might prove useful for the treatment of human malignancies. NEDD8-activating enzyme (NAE) is an essential component of the NEDD8 conjugation pathway that controls the activity of the cullin-RING subtype of ubiquitin ligases, thereby regulating the turnover of a subset of proteins upstream of the proteasome. Substrates of cullin-RING ligases have important roles in cellular processes associated with cancer cell growth and survival pathways. Here we describe MLN4924, a potent and selective inhibitor of NAE. MLN4924 disrupts cullin-RING ligase-mediated protein turnover leading to apoptotic death in human tumour cells by a new mechanism of action, the deregulation of S-phase DNA synthesis. MLN4924 suppressed the growth of human tumour xenografts in mice at compound exposures that were well tolerated. Our data suggest that NAE inhibitors may hold promise for the treatment of cancer.
Comment in
-
Drug discovery: Fresh target for cancer therapy.Nature. 2009 Apr 9;458(7239):709-10. doi: 10.1038/458709a. Nature. 2009. PMID: 19360071 No abstract available.
Similar articles
-
Mutations in UBA3 confer resistance to the NEDD8-activating enzyme inhibitor MLN4924 in human leukemic cells.PLoS One. 2014 Apr 1;9(4):e93530. doi: 10.1371/journal.pone.0093530. eCollection 2014. PLoS One. 2014. PMID: 24691136 Free PMC article.
-
Targeting NEDD8-activated cullin-RING ligases for the treatment of cancer.Clin Cancer Res. 2009 Jun 15;15(12):3912-6. doi: 10.1158/1078-0432.CCR-09-0343. Epub 2009 Jun 9. Clin Cancer Res. 2009. PMID: 19509147
-
Nedd8-Activating Enzyme Is a Druggable Host Dependency Factor of Human and Mouse Cytomegalovirus.Viruses. 2021 Aug 14;13(8):1610. doi: 10.3390/v13081610. Viruses. 2021. PMID: 34452475 Free PMC article.
-
Targeting Neddylation pathways to inactivate cullin-RING ligases for anticancer therapy.Antioxid Redox Signal. 2014 Dec 10;21(17):2383-400. doi: 10.1089/ars.2013.5795. Epub 2014 Feb 20. Antioxid Redox Signal. 2014. PMID: 24410571 Free PMC article. Review.
-
MLN4924: a novel first-in-class inhibitor of NEDD8-activating enzyme for cancer therapy.Expert Opin Investig Drugs. 2012 Oct;21(10):1563-73. doi: 10.1517/13543784.2012.707192. Epub 2012 Jul 16. Expert Opin Investig Drugs. 2012. PMID: 22799561 Review.
Cited by
-
Src phosphorylation converts Mdm2 from a ubiquitinating to a neddylating E3 ligase.Proc Natl Acad Sci U S A. 2015 Feb 10;112(6):1749-54. doi: 10.1073/pnas.1416656112. Epub 2015 Jan 26. Proc Natl Acad Sci U S A. 2015. PMID: 25624478 Free PMC article.
-
Neutrophils and inflammatory resolution in the mucosa.Semin Immunol. 2015 May;27(3):177-83. doi: 10.1016/j.smim.2015.03.007. Epub 2015 Mar 26. Semin Immunol. 2015. PMID: 25818531 Free PMC article. Review.
-
Convergence of mammalian RQC and C-end rule proteolytic pathways via alanine tailing.Mol Cell. 2021 May 20;81(10):2112-2122.e7. doi: 10.1016/j.molcel.2021.03.004. Epub 2021 Apr 27. Mol Cell. 2021. PMID: 33909987 Free PMC article.
-
Comprehensive transcriptomic analysis of molecularly targeted drugs in cancer for target pathway evaluation.Cancer Sci. 2015 Jul;106(7):909-20. doi: 10.1111/cas.12682. Epub 2015 May 25. Cancer Sci. 2015. PMID: 25911996 Free PMC article.
-
Bridged Proteolysis Targeting Chimera (PROTAC) Enables Degradation of Undruggable Targets.J Am Chem Soc. 2022 Dec 14;144(49):22622-22632. doi: 10.1021/jacs.2c09255. Epub 2022 Nov 30. J Am Chem Soc. 2022. PMID: 36448571 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous