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Domanda fondamentale È sufficiente attaccare esclusivamente le CSC? Nessuno ha finora dimostrato che l'incapacità di self-renewal delle CSC sia sufficiente ad impedire lo sviluppo di un tumore Acute Promyelocytic Leukemia (APL) Myeloid differentiation Monoblast Promyelocytes PML Chr 15 RAR Chr 17 PML RAR t(15;17) Leukemia-free survival (%) Leukemogenesis is a multi-stage process Pre-leukemia At the pre-leukemic stage, hematopoiesis is apparently norma Molecular mechanism of PML-RAR action DNMT/HMTs RA From DeThe and C ATRA acts on bulk APL cells, and on LICs APL ATRA Tumor Recurrenc tumor grows back PML-RAR degradation Bulk Cells LICs Continuous treatment with HDACi is required for prolonging survival of leukemic mice Continuous treatment with HDACi is required for prolonging survival of leukemic mice rapid growing cells killed tumor grows back An assay to measure LICs Bulk LIC (Ly5.1+)) Vehicle Treatment No Effect Leukemic Cells (Ly5.2) Drug treatment Harvest leukemic cells (Ly5.2+) treated/untreated LIC Expansion Transplant in Limiting Dilutions (Ly5.1+) LIC Reduction An assay to measure LICs Bulk LIC (Ly5.1+) Vehicle Treatment No Effect Leukemic Cells (Ly5.2) Drug treatment Harvest leukemic cells (Ly5.2+) treated/untreated LIC Expansion Transplant in Limiting Dilutions (Ly5.1+) LIC Reduction ATRA treatment reduces LIC frequency ≈ 100 fold VPA spares LICs Limiting Dilution Vehicle LIC Frequency 2.5x10^4 VPA 3.9x10^4 Short-term inhibition of multiple HDACs with SAHA tackles LICs but does not prolong survival Survival LIC assay LIC Frequency Vehicle SAHA 2.5x10^4 2.3x10^6 In Summary… Leukemia ATRA Tumor Recurrenc ? SAHA VPA Bulk Cells LICs Eradication of APL by ATRA-SAHA-VPA No leukemic cells detectable