Department of Laboratory Medicine, The First Affiliated Hospital of Kunming Medical College, Kunming, Yunnan, China.
Leuk Res. 2011 Oct;35(10):1355-9. doi: 10.1016/j.leukres.2011.04.020. Epub 2011 May 13.
Activation-induced deaminase (AID), a cytidine deaminase, can accelerate the acquisition of BCR-ABL1 kinase domain mutations in human CML. In the present study, we investigated the expression of AID and Bcr-Abl in CML cells derived from 35 clinical patients. We found that both AID and Bcr-Abl were correlatively over-expressed in CML-LBC (lymphoid blast crisis) cells as compared with those in CML-CP (chronic phase) cells. AID expression was significantly decreased in CML-LBC cells after treated with arsenic trioxide, especially together with imatinib. We also observed satisfied therapy effects of As(2)O(3) and imatinib on patients with CML blast crisis. These data suggest that decreasing AID expression in CML-LBC by As(2)O(3) may be a promising approach to CML treatment.
激活诱导脱氨酶(AID)是一种胞嘧啶脱氨酶,可加速人类 CML 中 BCR-ABL1 激酶结构域突变的获得。在本研究中,我们研究了来自 35 例临床患者的 CML 细胞中 AID 和 Bcr-Abl 的表达。我们发现,与 CML-CP(慢性期)细胞相比,CML-LBC(淋巴母细胞危象)细胞中 AID 和 Bcr-Abl 均过度表达。三氧化二砷治疗后,CML-LBC 细胞中的 AID 表达明显降低,尤其是与伊马替尼联合治疗时。我们还观察到三氧化二砷和伊马替尼对 CML 急变期患者的治疗效果令人满意。这些数据表明,通过三氧化二砷降低 CML-LBC 中的 AID 表达可能是治疗 CML 的一种有前途的方法。