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Sphingolipid players in the leukemia arena
Authors:Clara Ricci  Francesco Onida  Riccardo Ghidoni
Affiliation:a Laboratory of Biochemistry and Molecular Biology, San Paolo University Hospital, Medical School, University of Milan, 20142 via A. di Rudinì, 8-Milan, Italy
b Fondazione Matarelli, 20121 Milan, Italy
c Fondazione Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, IRCCS, and University of Milan, 20122 Milan, Italy
Abstract:Sphingolipids function as bioactive mediators of different cellular processes, mostly proliferation, survival, differentiation and apoptosis, besides being structural components of cellular membranes. Involvement of sphingolipid metabolism in cancerogenesis was demonstrated in solid tumors as well as in hematological malignancies. Herein, we describe the main biological and clinical aspects of leukemias and summarize data regarding sphingolipids as mediators of apoptosis triggered in response to anti-leukemic agents and synthetic analogs as inducers of cell death as well. We also report the contribution of molecules that modulate sphingolipid metabolism to development of encouraging strategies for leukemia treatment. Finally we address how deregulation of sphingolipid metabolism is associated to occurrence of therapy resistance both in vitro and in vivo. Sphingolipids can be considered promising therapeutic tools alone or in combination with other compounds, as well as valid targets in the attempt to eradicate leukemia and overcome drug resistance.
Keywords:4-HPR, fenretinide   ALL, acute lymphoblastic leukemia   AML, acute myeloid leukemia   AMMoL, acute myelomonocytic leukemia   APL, acute promyelocytic leukemia   Ara-c, cytosine arabinoside   aSMase, acid sphingomyelinase   ATRA, all-trans retinoic acid   B-CLL, chronic B-cell lymphoid leukemia   Cer, Ceramide   CML, chronic myelogenous leukemia   D609, tricyclodecan-9-yl-xanthogenate   d-e-MAPP, (1S,2R)-d-erythro-2-(N-myristoylamino)-1-phenyl-1-propanol   DMS, N,N-Dimethylsphingosine   DNR, daunorubicin   doxo, doxorubicin   DT, diphtheria toxin   EBV, Epstein-Barr Virus   Epo, erythropoietin   GCS, GlucosylCeramideSynthase   GlcCer, GlucosylCeramide   GM-CSF, granulocyte-macrophage colony-stimulating factor   GSH, glutathione   HDACIs, histone deacetylases inhibitors   HSC, hematopoietic stem cells   IM, Imatinib Mesylate   IR, ionizing radiation   LSC, leukemic stem cells   nSMase, neutral sphingomyelinase   Pgp, P-glycoprotein   Ph, Philadelphia Chromosome   PKC, protein kinases C   PPPP, dl-threo-phenyl-2-hexadecanoylamino-3-pyrrolidino-1-propanol   ROS, reactive oxygen species   S1P, sphingosine-1-phosphate   SAHA, suberoylanilide hydroximic acid   SK1, sphingosine kinase 1   SM, sphingomyelin   SMS, sphingomyelin synthase   SPLs, sphingolipids   SPT, serine-palmitoyl transferase   T-ALL, acute T-lymphoblastic leukemia   VCR, vincristine
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