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- W3201327672 abstract "We explored the anticancer activity of two synthetic flavonoid-based small molecules, HMDC and HMDF, with bioactive methylenedioxy functionality. HMDF inhibited the proliferation of the p53 wild-type (NCIH460 and A549), and p53 null (NCIH1299) non-small cell lung cancer and breast cancer (MCF-7) cells more potently than HMDC without significant cytotoxic effects on the normal lung-epithelial (L132) and macrophage (Raw 264.7) cells. HMDF mediated reduction of the cell proliferation occurred due to its attachment at the p53-binding domain of MDM2 (also evident from molecular docking analysis), which induced the disruption of the p53-MDM2 interactions. Ultimately, a higher expression of p53 in the NCIH460 cells was observed. The up-regulated p53 level instigated apoptosis of cancer cells. However, MDM2 expression level remained unaltered. The docking studies further indicate that HMDF can suppress the anti-apoptotic activity of Bcl-2 protein by blocking its BH3 domain." @default.
- W3201327672 created "2021-09-27" @default.
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- W3201327672 date "2022-01-01" @default.
- W3201327672 modified "2023-09-23" @default.
- W3201327672 title "Understanding the Role of Flavonoid Based Small Molecules in Modulating the Oncogenic Protein-Protein Interactions: A Quest for Therapeutic Arsenal" @default.
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- W3201327672 doi "https://doi.org/10.1016/j.molstruc.2021.131511" @default.
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