Please use this identifier to cite or link to this item: http://hdl.handle.net/2080/5502
Title: Shikonin-Induced Mitochondrial Apoptosis: Amplifying Reactive Oxygen Species and DNA Damage to Combat Oral Cancer
Authors: Khamari, Ashish Kumar
Biswal, Stuti
Biswal, Bijesh Kumar
Keywords: Shikonin
Reactive oxygen species
DNA damage
Oral cancer
Issue Date: Dec-2025
Citation: 94th Annual Meeting of SBC(I) and International Conference on Biological Communications in Disease and Development (ICBCDD), University of Hyderabad, Telangana, 17-19 December 2025
Abstract: Phytotherapy has provided a new insight into the treatment of many cancers, including oral cancer, over conventional chemotherapeutic agents, as it has lower side effects Shikonin ( is a naturally biologically active alkaloid found in the roots of the Lithospermum erythrorhizon plant, which exhibits strong cytotoxic effects against various cancers, including oral cancer The present study evaluates the anticancer efficacy of Shk in SCC 9 and H 357 oral cancer cell lines, emphasising its antiproliferative antimigratory and apoptosis inducing mechanisms We performed a series of assays, such as MTT, colony assay, wound healing, tumorsphere formation assay, AO/EtBr, DAPI, comet assay, western blotting, and measurements of reactive oxygen species ( and mitochondrial membrane potential ( As a result, we found that Shk reduced the viability, proliferation, and tumorigenicity of SCC 9 and H 357 cells in a time and concentration dependent manner It promotes apoptosis via overexpressing proapoptotic Bax and caspase 3 by enhancing ROS, that leads to MMP depletion and DNA damage Moreover, Shk inhibited cell migration by regulating epithelial mesenchymal transition ( markers, including the upregulation of E cadherin and ZO 1 expression and downregulation of N cadherin and vimentin Overall, our findings suggest that Shk possesses strong anticancer potential against oral cancer cells, highlighting its promise as a potential therapeutic agent for oral cancer treatment.
Description: Copyright belongs to the proceeding publisher.
URI: http://hdl.handle.net/2080/5502
Appears in Collections:Conference Papers

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