13rd Year Post Graduate, Department of Pharmacology, Third Floor, Medical College Block, SRMC and RI, Sri Ramachandra Institute of Higher Education and Research, No.1 Ramachandra Nagar, Porur, Chennai - 600 116, Tamil Nadu, India
2Professor and Head of the Department, Department of Pharmacology, Third Floor, Medical College Block, SRMC and RI, Sri Ramachandra Institute of Higher Education and Research, No.1 Ramachandra Nagar, Porur, Chennai - 600 116, Tamil Nadu, India
3Associate Professor, Department of Pharmacology, Third Floor, Medical College Block, SRMC and RI, Sri Ramachandra Institute of Higher Education and Research, No.1 Ramachandra Nagar, Porur, Chennai - 600 116, Tamil Nadu, India
*Corresponding Author E-mail: jennifermonica945@gmail.com
Online Published on 15 May, 2025.
With approximately ten million deaths from cancer in 2020, cancer is a major cause of death worldwide. In 2020, around 25% of newly diagnosed cancer patients will have a breast cancer, which has the highest incidence rates. Furthermore, one-third of female cancer patients under 60 have breast cancer, and the disease accounts for 18% of cancer-related deaths.In- vitro, in- silico and gene expression studies were done to assess the 7,3′-dihydroxyflavone’s anti-proliferative and pro-apoptotic activity. First, we used the MTT assay to show that 7,3′-dihydroxyflavone had anti-proliferative properties. Second, we assessed the apoptotic activity, which was verified by the Propidium Iodide Assay and Annexin V, which showed cells at every stage of the process. Third, we investigated the gene expression level of p53, p21, and Nfkb by RT-PCR analysis. Fourth, we studied the binding affinity of 7,3′-dihydroxyflavone against p53, p21, and Nfkb by cellular docking and protein-ligand interaction studies. Molecular docking of 7,3′- dihydroxyflavone were performed against p53, p21, and Nkfb receptors by using AutoDock Vina. An ADMET predictions was performed to inspect the chance of 7,3′-dihydroxyflavone being anti-cancer drug.
7,3′-dihydroxyflavone, MTT, P53, P21, Nfkb, RT-PCR, Molecular docking, ADMET