Riyahi Niknam, Safaroghli-Azar Ava, Sheikh-Zeineddini Negar, Sayyadi Mohamad, Bashash Davood
Student Research Committee, Department of Hematology and Blood Banking, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences , Tehran , Iran.
Department of Hematology and Blood Banking, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences , Tehran , Iran.
Cancer Invest. 2019;37(7):311-324. doi: 10.1080/07357907.2019.1651328. Epub 2019 Aug 14.
Enthusiasms into the application of PI3K-δ inhibitor CAL-101 has been muted due to the over-activation of compensatory molecules. Our results delineated that c-Myc suppression using 10058-F4 enhanced CAL-101 cytotoxicity in less sensitive cells through different mechanisms based on p53 status; while CAL-101-plus-10058-F4 induced G1 arrest in wild-type p53-expressing leukemic cells, no conspicuous increase in G1 was noted in U937 cells harboring mutant p53. Conclusively, this study shed lights on the role of c-Myc oncoprotein in acute leukemia cells sensitivity to PI3K inhibitor and outlined that the combination of c-Myc inhibitor and CAL-101 may be a promising therapeutic approach in leukemia.
由于补偿性分子的过度激活,PI3K-δ抑制剂CAL-101的应用热情有所降温。我们的结果表明,使用10058-F4抑制c-Myc可通过基于p53状态的不同机制增强CAL-101在低敏感性细胞中的细胞毒性;虽然CAL-101加10058-F4在表达野生型p53的白血病细胞中诱导G1期阻滞,但在携带突变型p53的U937细胞中未观察到G1期有明显增加。总之,本研究揭示了c-Myc癌蛋白在急性白血病细胞对PI3K抑制剂敏感性中的作用,并概述了c-Myc抑制剂与CAL-101联合使用可能是白血病一种有前景的治疗方法。