Litcius/Paper detail

Tanshinone IIA synergistically enhances the antitumor activity of doxorubicin by interfering with the PI3K/AKT/mTOR pathway and inhibition of topoisomerase II: <i>in vitro</i> and molecular docking studies

Aml Ghanem, Hamdy A. Emara, Shaden Muawia, Ahmed I. Abd El Maksoud, Ahmed A. Al‐Karmalawy, Mohamed F. Elshal

2020New Journal of Chemistry91 citationsDOI

Abstract

Schematic diagram showing the pharmacophoric features of doxorubicin and tanshinone IIA as DNA intercalators, and their effects on cardiac tissues.

Topics & Concepts

ChemistryPI3K/AKT/mTOR pathwayTopoisomeraseIn vitroDoxorubicinDocking (animal)Protein kinase BPharmacologyPhosphorylationBiochemistrySignal transductionChemotherapyNursingSurgeryMedicineCancer therapeutics and mechanismsTraditional Chinese Medicine AnalysisCancer Treatment and Pharmacology
Tanshinone IIA synergistically enhances the antitumor activity of doxorubicin by interfering with the PI3K/AKT/mTOR pathway and inhibition of topoisomerase II: <i>in vitro</i> and molecular docking studies | Litcius