| Literature DB >> 31412710 |
Niknam Riyahi1, Ava Safaroghli-Azar1, Negar Sheikh-Zeineddini1, Mohamad Sayyadi1, Davood Bashash2.
Abstract
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.Entities:
Keywords: 10058-F4; Acute leukemia; CAL-101; PI3K pathway; c-Myc
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Year: 2019 PMID: 31412710 DOI: 10.1080/07357907.2019.1651328
Source DB: PubMed Journal: Cancer Invest ISSN: 0735-7907 Impact factor: 2.176