Tinospora Cordifolia (Thunb.) Miers (Giloy) Inhibits Oral Cancer Cells In A Dose-Dependent Manner By Inducing Apoptosis And Attenuating Epithelial-Mesenchymal Transition

SAUDI JOURNAL OF BIOLOGICAL SCIENCES(2021)

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摘要
Background: Tinospora cordifolia (Thunb.) Miers (Giloy) has been applied successfully as an antiinflammatory, anti-diabetic, and even as an anti-cancer agent. Yet, to date, the application of Giloy has not been explored concerning oral cancer.Objectives: To assess the effect of T cordifolia (Thunb.) Miers (Giloy) extract (TcE) on an oral cancer cell line.Methods: AW13516 (oral cancer cell line) cells were treated with the prepared aqueous extract of TcE for 24 hat various concentrations ranging between 5 lg/ml and 100 lg/ml and compared with control (cells without treatment). Thee effect of the extracts on apoptosis was assessed by through Annexin V flow cytometry assay and Luminometry based assessment of Caspase 8, 9 and caspase 3/7 activity. RNA was isolated from treated cells and gene expression of selected metastatic genes (MMP1, MMP10, and CXCL8); epithelial-mesenchymal stem cell genes (TWIST1, SNAIL, ZEB1, Oct4) and stemness related genses (Nanog, Sox2) were analyzed by using a quantitative real-time PCR system. The experiments were performed in triplicates.Results: Aqueous extract of TcE was found to induce apoptosis inducer in AW13516 cells in a concentration-dependent manner and was potent even at a low concentration of 5 lg/ml. The apoptosis induction was confirmed with the caspase activity assay. Treatment of the cells with the extract for 24 h exhibited a significant decrease in the expression of EMT genes in a dose-dependent manner without an effect on the metastatic genes.Conclusion: Aqueous extract of TcE induces apoptosis-mediated cell death in the oral cancer cell line AW13516 while attenuating its potential for epithelial mesenchymal transition. (C) 2021 The Author(s). Published by Elsevier B.V. on behalf of King Saud University.
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关键词
Giloy, Oral cancer, AW13516 cell line, Apoptosis, Epithelial-mesenchymal transition, Mitochondrial membrane potential
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