Zuccato Cristina, Bianchi Nicoletta, Borgatti Monica, Lampronti Ilaria, Massei Francesco, Favre Claudio, Gambari Roberto
GenTech-for-Thal, Department of Biochemistry and Molecular Biology, University of Ferrara, Ferrara, Italy.
Acta Haematol. 2007;117(3):168-76. doi: 10.1159/000097465. Epub 2006 Dec 5.
We studied the effects of everolimus on the erythroid differentiation of human leukaemic K562 cells and on the cultures of erythroid progenitors derived from the peripheral blood of beta-thalassaemia patients. A quantitative real-time reverse-transcription polymerase chain reaction assay was employed for the quantification of the accumulation of globin mRNAs. The results obtained demonstrate that everolimus is a potent inducer of the erythroid differentiation of K562 cells. Erythroid induction is associated with an increase in alpha- and gamma-globin mRNAs. In erythroid precursor cells from 4 beta-thalassaemia patients, everolimus stimulated a preferential increase (ranging from 1.8- to 7.2-fold) in gamma-globin mRNA. Only minor effects were observed on the expression of alpha-globin genes. These results, in our opinion, are of interest as this compound is already employed in clinical trials as an anti-rejection agent following kidney transplantation. These data suggest that everolimus warrants further evaluation as a potential therapeutic drug in the treatment of beta-thalassaemia.
我们研究了依维莫司对人白血病K562细胞红系分化以及对β地中海贫血患者外周血来源的红系祖细胞培养的影响。采用定量实时逆转录聚合酶链反应分析法定量珠蛋白mRNA的积累。获得的结果表明,依维莫司是K562细胞红系分化的有效诱导剂。红系诱导与α和γ珠蛋白mRNA的增加有关。在4例β地中海贫血患者的红系前体细胞中,依维莫司刺激γ珠蛋白mRNA优先增加(1.8至7.2倍)。对α珠蛋白基因的表达仅观察到轻微影响。我们认为,这些结果很有意义,因为该化合物已作为肾移植后的抗排斥药物用于临床试验。这些数据表明,依维莫司作为治疗β地中海贫血的潜在治疗药物值得进一步评估。