HIV Protease Inhibitors for the Treatment of Multiple Myeloma

被引:0
作者
Mendez-Lopez, Max [1 ]
Sutter, Tabea [1 ]
Driessen, Christoph [1 ]
Besse, Lenka [1 ]
机构
[1] Cantonal Hosp St Gallen, Dept Med Oncol & Hematol, Rorschacherstr 95, CH-9007 St Gallen, Switzerland
关键词
Drug repurposing; HIV protease inhibitors; multiple myeloma; proteasome inhibitors; ENDOPLASMIC-RETICULUM STRESS; BONE-MARROW ANGIOGENESIS; SINGLE-AGENT CARFILZOMIB; LOW-DOSE DEXAMETHASONE; CELLS IN-VITRO; ANTIRETROVIRAL THERAPY; DRUG-RESISTANCE; GROWTH ARREST; MICROVESSEL DENSITY; INITIAL THERAPY;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Outcomes in multiple myeloma (MM) patients have improved in recent years owing to the introduction of new drugs. Among them, proteasome inhibitors and immunomodulatory imide drugs have become central in the management of newly diagnosed and relapsed MM. However, resistance to these classes of agents develops in most patients and ultimately leads to death from relapsed/refractory disease. A need exists for new classes of antimyeloma drugs, especially ones that are active in the multirefractory setting. The conventional drug development process, which involves extensive preclinical and clinical testing prior to assessment of clinical activity, has fallen short in delivering adequately safe and active novel drug candidates. HIV protease inhibitors such as nelfinavir are safe, US Food and Drug Administration-approved agents that have been shown to have potent antimyeloma activity in both preclinical models and patients with refractory disease. The repurposing of HIV protease inhibitors for treatment of MM is promising in light of their antimyeloma activity in conjunction with their global availability, established safety, and relatively low cost. This review will summarize the preclinical and clinical data available on HIV protease inhibitors for the treatment of refractory MM.
引用
收藏
页码:615 / 623
页数:9
相关论文
共 109 条
  • [1] An inhibitor of HIV-1 protease modulates proteasome activity, antigen presentation, and T cell responses
    André, P
    Groettrup, M
    Klenerman, P
    de Giuli, R
    Booth, BL
    Cerundolo, V
    Bonneville, M
    Jotereau, F
    Zinkernagel, RM
    Lotteau, V
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) : 13120 - 13124
  • [2] Drug repositioning: Identifying and developing new uses for existing drugs
    Ashburn, TT
    Thor, KB
    [J]. NATURE REVIEWS DRUG DISCOVERY, 2004, 3 (08) : 673 - 683
  • [3] Bahlis NJ, 2016, BLOOD S, V128
  • [4] The HIV protease inhibitor indinavir down-regulates the expression of the pro-angiogenic MT1-MMP by human endothelial cells
    Barillari, Giovanni
    Iovane, Andre
    Bacigalupo, Ilaria
    Labbaye, Catherine
    Chiozzini, Chiara
    Sernicola, Leonardo
    Quaranta, Maria Teresa
    Falchi, Mario
    Sgadari, Cecilia
    Ensoli, Barbara
    [J]. ANGIOGENESIS, 2014, 17 (04) : 831 - 838
  • [5] ISOLATION OF A T-LYMPHOTROPIC RETROVIRUS FROM A PATIENT AT RISK FOR ACQUIRED IMMUNE-DEFICIENCY SYNDROME (AIDS)
    BARRESINOUSSI, F
    CHERMANN, JC
    REY, F
    NUGEYRE, MT
    CHAMARET, S
    GRUEST, J
    DAUGUET, C
    AXLERBLIN, C
    VEZINETBRUN, F
    ROUZIOUX, C
    ROZENBAUM, W
    MONTAGNIER, L
    [J]. SCIENCE, 1983, 220 (4599) : 868 - 871
  • [6] Association between altered expression of adipogenic factor SREBP1 in lipoatrophic adipose tissue from HIV-1-infected patients and abnormal adipocyte differentiation and insulin resistance
    Bastard, JP
    Caron, M
    Vidal, H
    Jan, V
    Auclair, M
    Vigouroux, C
    Luboinski, J
    Laville, M
    Malachi, M
    Girard, PM
    Rozenbaum, W
    Levan, P
    Capeau, J
    [J]. LANCET, 2002, 359 (9311) : 1026 - 1031
  • [7] Carfilzomib resistance due to ABCB1/MDR1 overexpression is overcome by nelfinavir and lopinavir in multiple myeloma
    Besse, A.
    Stolze, S. C.
    Rasche, L.
    Weinhold, N.
    Morgan, G. J.
    Kraus, M.
    Bader, J.
    Overkleeft, H. S.
    Besse, L.
    Driessen, C.
    [J]. LEUKEMIA, 2018, 32 (02) : 391 - 401
  • [8] A metabolic switch in proteasome inhibitor-resistant multiple myeloma ensures higher mitochondrial metabolism, protein folding and sphingomyelin synthesis
    Besse, Lenka
    Besse, Andrej
    Mendez-Lopez, Max
    Vasickova, Katerina
    Sedlackova, Miroslava
    Vanhara, Petr
    Kraus, Marianne
    Bader, Jurgen
    Ferreira, Renan B.
    Castellano, Ronald K.
    Law, Brian K.
    Driessen, Christoph
    [J]. HAEMATOLOGICA, 2019, 104 (09)
  • [9] The human immunodeficiency virus-1 protease inhibitor nelfinavir impairs proteasome activity and inhibits the proliferation of multiple myeloma cells in vitro and in vivo
    Bono, Camille
    Karlin, Lionel
    Hare, Stephanie
    Mouly, Enguerran
    Labaume, Sylvaine
    Galicier, Lionel
    Apcher, Sebastien
    Sauvageon, Helene
    Fermand, Jean-Paul
    Bories, Jean-Christophe
    Arnulf, Bertrand
    [J]. HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2012, 97 (07): : 1101 - 1109
  • [10] Brüning A, 2009, CANCER BIOL THER, V8, P222