Literature DB >> 25188480

Current advances in novel proteasome inhibitor-based approaches to the treatment of relapsed/refractory multiple myeloma.

Sagar Lonial, Lawrence H Boise.   

Abstract

Proteasome inhibitors (PIs) are a proven class of therapeutic agents in the treatment of cancers including multiple myeloma (MM), Waldenstrm macroglobulinemia, and mantle cell lymphoma. Their primary target is the ubiquitin-proteasome system, a universal component of eukaryotic cells involved in regulation of cellular homeostasis, angiogenesis, and cell death. Bortezomib (Velcade) is a potent and reversible PI that has been used successfully in the treatment of patients with MM. While the use of bortezomib has helped to change the natural history of MM, it is not universally effective and is associated with reversible peripheral neuropathy that can limit short-term and long-term use. Newer PIs, some of which are now undergoing clinical investigation, offer several potential advantages over bortezomib, including greater specificity and improved safety and tolerability. Here we provide a summary of the PIs in clinical and preclinical development.

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Year:  2011        PMID: 25188480

Source DB:  PubMed          Journal:  Oncology (Williston Park)        ISSN: 0890-9091            Impact factor:   2.990


  4 in total

Review 1.  Dysproteinemias and Glomerular Disease.

Authors:  Nelson Leung; Maria E Drosou; Samih H Nasr
Journal:  Clin J Am Soc Nephrol       Date:  2017-11-07       Impact factor: 8.237

2.  The combination of ionizing radiation and proteasomal inhibition by bortezomib enhances the expression of NKG2D ligands in multiple myeloma cells.

Authors:  Young Shin Lee; Woong Heo; Jiho Nam; Young Hwa Jeung; Jaeho Bae
Journal:  J Radiat Res       Date:  2018-05-01       Impact factor: 2.724

3.  Downregulation of PA28α induces proteasome remodeling and results in resistance to proteasome inhibitors in multiple myeloma.

Authors:  Yanyan Gu; Benjamin G Barwick; Mala Shanmugam; Craig C Hofmeister; Jonathan Kaufman; Ajay Nooka; Vikas Gupta; Madhav Dhodapkar; Lawrence H Boise; Sagar Lonial
Journal:  Blood Cancer J       Date:  2020-12-14       Impact factor: 11.037

4.  FV-162 is a novel, orally bioavailable, irreversible proteasome inhibitor with improved pharmacokinetics displaying preclinical efficacy with continuous daily dosing.

Authors:  Z Wang; P Dove; X Wang; A Shamas-Din; Z Li; A Nachman; Y J Oh; R Hurren; A Ruschak; S Climie; B Press; C Griffin; E Undzys; A Aman; R Al-awar; L E Kay; D O'Neill; S Trudel; M Slassi; A D Schimmer
Journal:  Cell Death Dis       Date:  2015-07-09       Impact factor: 8.469

  4 in total

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