PI3K/AKT/mTOR通路
癌症研究
白血病
突变体
U937电池
细胞毒性
化学
生物
细胞凋亡
免疫学
体外
生物化学
基因
作者
Niknam Riyahi,Ava Safaroghli‐Azar,Negar Sheikh‐Zeineddini,Mohammad Sayyadi,Davood Bashash
标识
DOI:10.1080/07357907.2019.1651328
摘要
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.
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