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Development of certain benzylidene coumarin derivatives as anti-prostate cancer agents targeting EGFR and PI3Kβ kinases

Lina M. A. Abdel Ghany, Tarek S. Ibrahim, Abdulrahman S. Alharbi, Mohamed S. Abdel‐Aziz, Eman M. El‐labbad, Mohamed Elagawany, Noha Ryad

2024Journal of Enzyme Inhibition and Medicinal Chemistry11 citationsDOIOpen Access PDF

Abstract

Novel coumarin derivatives were synthesised and tested for their cytotoxicity against human cancer cells (PC-3 and MDA-MB-231). Compounds 5, 4b, and 4a possessed potent cytotoxic activity against PC-3 cells with IC50 3.56, 8.99, and 10.22 µM, respectively. Compound 4c displayed cytotoxicity more than erlotinib in the MDA-MB-231 cells with IC50 8.5 µM. Moreover, compound 5 exhibited potent inhibitory activity on EFGR with IC50 0.1812 µM, as well as PI3Kβ inhibitory activity that was twofold higher than LY294002, suggesting that this compound has a dual EGFR and PI3Kβ inhibiting activity. Docking aligns with the in vitro results and sheds light on the molecular mechanisms underlying dual targeting. Furthermore, compound 5 decreased AKT and m-TOR expression in PC-3 cells, showing that it specifically targets these cells via the EGFR/PI3K/Akt/m-TOR signalling pathway. Simultaneously, compound 5 caused cell cycle arrest at S phase and induced activation of both intrinsic and extrinsic apoptotic pathways.

Topics & Concepts

ChemistryCytotoxicityPI3K/AKT/mTOR pathwayProtein kinase BCoumarinDocking (animal)IC50In vitroCancer cellLY294002ErlotinibApoptosisCytotoxic T cellEGFR inhibitorsKinaseCancer researchPharmacologyBiochemistryEpidermal growth factor receptorCancerReceptorBiologyMedicineNursingGeneticsOrganic chemistryPI3K/AKT/mTOR signaling in cancerQuinazolinone synthesis and applicationsSynthesis and biological activity
Development of certain benzylidene coumarin derivatives as anti-prostate cancer agents targeting EGFR and PI3Kβ kinases | Litcius