MLN4924: a novel first-in-class inhibitor of NEDD8-activating enzyme for cancer therapy

Introduction: The small ubiquitin-like molecule NEDD8 has been identified as an essential regulator of the activity of the cullin-RING E3 ubiquitin ligases (CRLs), which control the turnover of multiple proteins with fundamental roles in cancer biology. The aberrant function of the NEDD8 cascade within the context of malignancy makes it an attractive target for the development of novel anticancer agents. MLN4924 is a first-in-class inhibitor of the proximal regulator of the NEDD8 system (NEDD8-activating enzyme, NAE) that has entered Phase-I trials for cancer therapy and has established that significant therapeutic benefit can be achieved by antagonizing NEDD8-mediated protein degradation. Areas covered: This review provides a detailed overview of the NEDD8 system and discusses the mechanisms of action of MLN4924, a novel small molecule NAE inhibitor. Key findings from preclinical investigations of MLN4924 in a broad range of cancer models and preliminary findings from ongoing Phase-I clinical trials with MLN4924 are also discussed. Expert opinion: Targeting protein NEDDylation represents an exciting new anticancer strategy with demonstrable therapeutic benefit. Ongoing and future studies focused on dissecting the functional status/regulation of the NEDD8 system in individual tumor types will facilitate the design of novel approaches that yield optimal therapeutic benefit.

[1]  D. C. Dias,et al.  Nedd8 on cullin: building an expressway to protein destruction , 2004, Oncogene.

[2]  J. Wade Harper,et al.  Drug discovery in the ubiquitin–proteasome system , 2006, Nature Reviews Drug Discovery.

[3]  A. Haas,et al.  The mechanism of ubiquitin activating enzyme. A kinetic and equilibrium analysis. , 1982, The Journal of biological chemistry.

[4]  H. Gundacker,et al.  Age and acute myeloid leukemia. , 2006, Blood.

[5]  V. Chau,et al.  Nedd8 Modification of Cul-1 Activates SCFβTrCP-Dependent Ubiquitination of IκBα , 2000, Molecular and Cellular Biology.

[6]  Yi Sun,et al.  The p21-Dependent Radiosensitization of Human Breast Cancer Cells by MLN4924, an Investigational Inhibitor of NEDD8 Activating Enzyme , 2012, PloS one.

[7]  A. Ciechanover,et al.  Narrative Review: Protein Degradation and Human Diseases: The Ubiquitin Connection , 2006, Annals of Internal Medicine.

[8]  E. Lightcap,et al.  A Nedd8 conjugation pathway is essential for proteolytic targeting of p27Kip1 by ubiquitination. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[9]  E. Yeh,et al.  Identification of NEDD8-conjugation site in human cullin-2. , 1999, Biochemical and biophysical research communications.

[10]  Anjanabha Saha,et al.  Multimodal activation of the ubiquitin ligase SCF by Nedd8 conjugation , 2008, Molecular cell.

[11]  Keiji Tanaka,et al.  Cullin-based ubiquitin ligase and its control by NEDD8-conjugating system. , 2004, Current protein & peptide science.

[12]  M. Roussel,et al.  E2-RING expansion of the NEDD8 cascade confers specificity to cullin modification. , 2009, Molecular cell.

[13]  Ash A. Alizadeh,et al.  Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling , 2000, Nature.

[14]  F. Melchior,et al.  Concepts in sumoylation: a decade on , 2007, Nature Reviews Molecular Cell Biology.

[15]  Aaron Ciechanover,et al.  The ubiquitin–proteasome pathway: on protein death and cell life , 1998, The EMBO journal.

[16]  M. Petroski,et al.  The ubiquitin system, disease, and drug discovery , 2008, BMC Biochemistry.

[17]  S. Todo,et al.  TRIM40 promotes neddylation of IKKγ and is downregulated in gastrointestinal cancers. , 2011, Carcinogenesis.

[18]  M. Hochstrasser,et al.  Origin and function of ubiquitin-like proteins , 2009, Nature.

[19]  Kongthawat Chairatvit,et al.  Control of cell proliferation via elevated NEDD8 conjugation in oral squamous cell carcinoma , 2007, Molecular and Cellular Biochemistry.

[20]  Jidong Liu,et al.  NEDD8 modification of CUL1 dissociates p120(CAND1), an inhibitor of CUL1-SKP1 binding and SCF ligases. , 2002, Molecular cell.

[21]  Mark Manfredi,et al.  MLN4924, a NEDD8-activating enzyme inhibitor, is active in diffuse large B-cell lymphoma models: rationale for treatment of NF-{kappa}B-dependent lymphoma. , 2010, Blood.

[22]  H. Suzuki,et al.  NEDD8 recruits E2‐ubiquitin to SCF E3 ligase , 2001, The EMBO journal.

[23]  A. Ciechanover,et al.  The ubiquitin-proteasome pathway: the complexity and myriad functions of proteins death. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[24]  J. Wade Harper,et al.  Ubiquitin-like protein activation by E1 enzymes: the apex for downstream signalling pathways , 2009, Nature Reviews Molecular Cell Biology.

[25]  Jeffrey J. Jones,et al.  A targeted proteomic analysis of the ubiquitin-like modifier nedd8 and associated proteins. , 2008, Journal of proteome research.

[26]  R. Neve,et al.  The Amyloid Precursor Protein-binding Protein APP-BP1 Drives the Cell Cycle through the S-M Checkpoint and Causes Apoptosis in Neurons* , 2000, The Journal of Biological Chemistry.

[27]  Hartmut Goldschmidt,et al.  Bortezomib or high-dose dexamethasone for relapsed multiple myeloma. , 2005, The New England journal of medicine.

[28]  Hui Zhang,et al.  CAND1 binds to unneddylated CUL1 and regulates the formation of SCF ubiquitin E3 ligase complex. , 2002, Molecular cell.

[29]  A. Hershko,et al.  The ubiquitin system for protein degradation and some of its roles in the control of the cell division cycle* , 2005, Cell Death and Differentiation.

[30]  A. Hershko,et al.  Regulation of neddylation and deneddylation of cullin1 in SCFSkp2 ubiquitin ligase by F-box protein and substrate. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[31]  J. Laubach,et al.  Clinical challenges associated with bortezomib therapy in multiple myeloma and Waldenströms Macroglobulinemia , 2009, Leukemia & lymphoma.

[32]  Francis J Giles,et al.  Inhibition of NEDD8-activating enzyme: a novel approach for the treatment of acute myeloid leukemia. , 2010, Blood.

[33]  P. Robinson,et al.  E3 ubiquitin ligases. , 2005, Essays in biochemistry.

[34]  Michele Cavo,et al.  Proteasome inhibitors in multiple myeloma: 10 years later. , 2012, Blood.

[35]  Daniel C. Scott,et al.  Structural Insights into NEDD8 Activation of Cullin-RING Ligases: Conformational Control of Conjugation , 2008, Cell.

[36]  J. Toth,et al.  A gatekeeper residue for NEDD8-activating enzyme inhibition by MLN4924. , 2012, Cell reports.

[37]  E. Yeh,et al.  Characterization of NEDD8, a Developmentally Down-regulated Ubiquitin-like Protein* , 1997, The Journal of Biological Chemistry.

[38]  L. Kay,et al.  Novel proteasome inhibitors to overcome bortezomib resistance. , 2011, Journal of the National Cancer Institute.

[39]  W. Kaelin,et al.  An intact NEDD8 pathway is required for Cullin‐dependent ubiquitylation in mammalian cells , 2002, EMBO reports.

[40]  Bhuvanesh Singh,et al.  SCCRO (DCUN1D1) Is an Essential Component of the E3 Complex for Neddylation* , 2008, Journal of Biological Chemistry.

[41]  A. Ciechanover Intracellular protein degradation: from a vague idea thru the lysosome and the ubiquitin–proteasome system and onto human diseases and drug targeting* , 2005, Cell Death and Differentiation.

[42]  E. Yeh,et al.  Identification of the Activating and Conjugating Enzymes of the NEDD8 Conjugation Pathway* , 1999, The Journal of Biological Chemistry.

[43]  D. Ribatti,et al.  Bortezomib as an antitumor agent. , 2006, Current pharmaceutical biotechnology.

[44]  Raymond J. Deshaies,et al.  Function and regulation of cullin–RING ubiquitin ligases , 2005, Nature Reviews Molecular Cell Biology.

[45]  B. Schulman,et al.  Expression, purification, and characterization of the E1 for human NEDD8, the heterodimeric APPBP1-UBA3 complex. , 2005, Methods in enzymology.

[46]  R. Deshaies,et al.  In vitro reconstitution of SCF substrate ubiquitination with purified proteins. , 2005, Methods in enzymology.

[47]  Tommer Ravid,et al.  Diversity of degradation signals in the ubiquitin–proteasome system , 2008, Nature Reviews Molecular Cell Biology.

[48]  E. Brambilla,et al.  Altered pattern of Cul-1 protein expression and neddylation in human lung tumours: relationships with CAND1 and cyclin E protein levels. , 2007, The Journal of pathology.

[49]  Y. Saeki,et al.  Direct interactions between NEDD8 and ubiquitin E2 conjugating enzymes upregulate cullin-based E3 ligase activity , 2007, Nature Structural &Molecular Biology.

[50]  N. Munshi,et al.  Latest advances and current challenges in the treatment of multiple myeloma , 2012, Nature Reviews Clinical Oncology.

[51]  S. Elledge,et al.  Structure of the Cul1–Rbx1–Skp1–F boxSkp2 SCF ubiquitin ligase complex , 2002, Nature.

[52]  Kenneth P Nephew,et al.  The NEDD8 pathway is required for proteasome-mediated degradation of human estrogen receptor (ER)-alpha and essential for the antiproliferative activity of ICI 182,780 in ERalpha-positive breast cancer cells. , 2003, Molecular endocrinology.

[53]  Amanda Doucette,et al.  An inhibitor of NEDD8-activating enzyme as a new approach to treat cancer , 2009, Nature.

[54]  A. Ciechanover,et al.  Targeting proteins for destruction by the ubiquitin system: implications for human pathobiology. , 2009, Annual review of pharmacology and toxicology.

[55]  David W. Miller,et al.  The structure of the APPBP1-UBA3-NEDD8-ATP complex reveals the basis for selective ubiquitin-like protein activation by an E1. , 2003, Molecular cell.

[56]  Yu Shyr,et al.  Survival in BRAF V600-mutant advanced melanoma treated with vemurafenib. , 2012, The New England journal of medicine.

[57]  A. Haas,et al.  Conservation in the Mechanism of Nedd8 Activation by the Human AppBp1-Uba3 Heterodimer* , 2003, Journal of Biological Chemistry.

[58]  Ping Li,et al.  Substrate-assisted inhibition of ubiquitin-like protein-activating enzymes: the NEDD8 E1 inhibitor MLN4924 forms a NEDD8-AMP mimetic in situ. , 2010, Molecular cell.

[59]  Anindya Dutta,et al.  NEDD8-targeting drug MLN4924 elicits DNA rereplication by stabilizing Cdt1 in S phase, triggering checkpoint activation, apoptosis, and senescence in cancer cells. , 2010, Cancer research.

[60]  S. Keir,et al.  Initial testing of the investigational NEDD8‐activating enzyme inhibitor MLN4924 by the pediatric preclinical testing program , 2012, Pediatric blood & cancer.

[61]  Bart Barlogie,et al.  A phase 2 study of bortezomib in relapsed, refractory myeloma. , 2003, The New England journal of medicine.

[62]  D. Kuhn,et al.  Proteasome Inhibitors in Cancer Therapy: Lessons from the First Decade , 2008, Clinical Cancer Research.

[63]  Hua Li,et al.  Radiosensitization of human pancreatic cancer cells by MLN4924, an investigational NEDD8-activating enzyme inhibitor. , 2012, Cancer research.

[64]  Ivan Dikic,et al.  Ubiquitin-binding proteins: decoders of ubiquitin-mediated cellular functions. , 2012, Annual review of biochemistry.

[65]  U. Narayanan,et al.  Inhibition of NEDD8-activating enzyme induces rereplication and apoptosis in human tumor cells consistent with deregulating CDT1 turnover. , 2011, Cancer research.

[66]  J. Andersen,et al.  The interferon regulated ubiquitin-like protein, ISG15, in tumorigenesis: friend or foe? , 2006, Cytokine & growth factor reviews.

[67]  Keiji Tanaka,et al.  Covalent modification of all members of human cullin family proteins by NEDD8 , 1999, Oncogene.

[68]  N. Munshi,et al.  Bortezomib in the front-line treatment of multiple myeloma , 2008, Expert Review of Anticancer Therapy.

[69]  Yi Sun,et al.  Targeting E3 Ubiquitin Ligases for Cancer Therapy , 2003, Cancer biology & therapy.

[70]  D. McMillin,et al.  Molecular and Cellular Effects of NEDD8-Activating Enzyme Inhibition in Myeloma , 2012, Molecular Cancer Therapeutics.

[71]  M. Hochstrasser,et al.  Modification of proteins by ubiquitin and ubiquitin-like proteins. , 2006, Annual review of cell and developmental biology.

[72]  Bin Jiang,et al.  Bortezomib plus melphalan and prednisone for initial treatment of multiple myeloma. , 2008, The New England journal of medicine.

[73]  M. Huang,et al.  Inhibition of the Nedd8 System Sensitizes Cells to DNA Interstrand Cross-linking Agents , 2012, Molecular Cancer Research.

[74]  M. Tyers,et al.  Dcn1 functions as a scaffold-type E3 ligase for cullin neddylation. , 2008, Molecular cell.

[75]  C. Hill,et al.  Crystal Structure of the Human Ubiquitin-like Protein NEDD8 and Interactions with Ubiquitin Pathway Enzymes* , 1998, The Journal of Biological Chemistry.

[76]  Usha Narayanan,et al.  Treatment-emergent mutations in NAEβ confer resistance to the NEDD8-activating enzyme inhibitor MLN4924. , 2012, Cancer cell.