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Rizzieri et al. J Cancer Metastasis Treat 2019;5:26                 Journal of Cancer
               DOI: 10.20517/2394-4722.2019.05                           Metastasis and Treatment




               Review                                                                        Open Access


               Metabolic alterations and the potential for targeting
               metabolic pathways in the treatment of multiple

               myeloma

               Dustin Rizzieri, Barry Paul, Yubin Kang


               Division of Hematological Malignancies and Cellular Therapy, Duke University Medical Center, Durham, NC 27710, USA.
               Correspondence to: Dr. Yubin Kang, Division of Hematological Malignancies and Cellular Therapy, Duke University Medical
               Center, DUMC 3961, 2400 Pratt Street, Suite 5000, Durham, NC 27710, USA. E-mail: yubin.kang@duke.edu
               How to cite this article: Rizzieri D, Paul B, Kang Y. Metabolic alterations and the potential for targeting metabolic pathways in the
               treatment of multiple myeloma. J Cancer Metastasis Treat 2019;5:26. http://dx.doi.org/10.20517/2394-4722.2019.05
               Received: 5 Jan 2019    First Decision: 30 Jan 2019     Revised: 15 Feb 2019     Accepted: 27 Feb 2019     Published: 3 Apr 2019

               Science Editor: Siddiqui Rafat     Copy Editor: Cai-Hong Wang    Production Editor: Huan-Liang Wu



               Abstract
               Metabolism is defined as the collection of complex biochemical processes that living cells use to generate energy and
               maintain their growth and survival. Metabolism encompasses the synthesis and breakdown of glucose, fatty acids,
               and amino acids; the generation of energy (ATP); and oxidative phosphorylation. In cancer cells, metabolism can be
               commandeered to promote tumor growth and cellular proliferation. These alterations in metabolism have emerged
               as an additional hallmark of various cancers. In this review we focus on metabolic alterations in multiple myeloma
               (MM) - a malignancy of plasma cells - including derangements in glycolysis, gluconeogenesis, the tricarboxylic acid
               cycle, oxidative phosphorylation, and fatty acid/amino acid synthesis and degradation. Particular focus is given
               to metabolic alterations that contribute to myeloma cell growth, proliferation and drug resistance. Finally, novel
               approaches that target metabolic pathways for the treatment of MM are discussed.


               Keywords: Metabolism, alterations, multiple myeloma, treatment




               MULTIPLE MYELOMA
               Multiple myeloma (MM) is a malignancy of terminally differentiated plasma cells typically characterized by
               clonal proliferation of these plasma cells in the bone marrow. MM represents 1% of all malignancies and 18% of
               hematologic malignancies in the United States; accounting for an estimated 30,770 new diagnoses and 12,770
                               [1]
               deaths in 2018 alone . Classically, MM results in the secretion of a non-functional monoclonal immunoglobulin

                           © The Author(s) 2019. Open Access This article is licensed under a Creative Commons Attribution 4.0
                           International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use,
                sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long
                as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license,
                and indicate if changes were made.


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