Sphingolipid players in the leukemia arena |
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Authors: | Clara Ricci Francesco Onida Riccardo Ghidoni |
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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 |
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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. |
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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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