CD38
生物
川地34
髓样
细胞培养
小RNA
髓系白血病
癌症研究
分子生物学
细胞生物学
遗传学
干细胞
基因
作者
Laura Pedranzini,Federica Mottadelli,Simona Ronzoni,Franca Rossella,Manuela Ferracin,Ivana Magnani,Gaia Roversi,Patrizia Colapietro,Massimo Negrini,Pier Giuseppe Pelicci,Lidia Larizza
标识
DOI:10.1016/j.leukres.2010.02.012
摘要
The t(8;21) Acute Myeloid Leukaemia (AML) Kasumi-1 cell line with N822K KIT mutation, is a model system for leukemogenesis. As AML initiating cells reside in the CD34+CD38− fraction, we addressed the refined cytogenomic characterization and miRNA expression of Kasumi-1 cell line and its FACS-sorted subpopulations focussing on this compartment. By conventional cytogenetics, Spectral-Karyotyping and array-CGH the cytogenomic profile of Kasumi-1 cells evidenced only subtle regions differentially represented in CD34+CD38− cells. Expression profiling by a miRNA platform showed a set of miRNA differentially expressed in paired subpopulations and the signature of miR-584 and miR-182 upregulation in the CD34+CD38− fraction.
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