Dipartimento di Medicina Clinica e Chirurgia, University of Naples Federico II, Italy; CEINGE Biotecnologie Avanzate, Napoli, Italy.
Dipartimento di Medicina Clinica e Chirurgia, University of Naples Federico II, Italy; CEINGE Biotecnologie Avanzate, Napoli, Italy.
Leuk Res. 2014 Feb;38(2):236-42. doi: 10.1016/j.leukres.2013.11.006. Epub 2013 Nov 15.
The IC50 of TKIs is significantly increased when BCR-ABL+ K562 cell line is cultured in stroma conditioned media produced by BM mesenchymal cells. In particular, while the Imatinib IC50 in the stromal co-cultures was well above the in vivo through levels of the drug, the IC50s of second generation TKIs were still below their through levels. Moreover, we provide a formal comparison of the synergy between first and second generation TKIs with the JAK inhibitor Ruxolitinib to overcome BM stroma related TKI resistance. Taken together, our data provide a rationale for the therapeutic combination of TKIs and Ruxolitinib with the aim to eradicate primary BCR-ABL+ cells homed in BM niches.
当 BCR-ABL+K562 细胞系在 BM 间质细胞产生的基质条件培养基中培养时,TKI 的 IC50 显著增加。特别是,当基质共培养物中的伊马替尼 IC50 远高于药物的体内水平时,第二代 TKI 的 IC50 仍低于其体内水平。此外,我们还对第一代和第二代 TKI 与 JAK 抑制剂芦可替尼之间的协同作用进行了正式比较,以克服 BM 基质相关 TKI 耐药性。总之,我们的数据为 TKI 和芦可替尼的联合治疗提供了依据,旨在根除归巢于 BM 龛中的原发性 BCR-ABL+细胞。