Nat Prod Sci.  2023 Dec;29(4):297-304. 10.20307/nps.2023.29.4.297.

Schisandrin C Protects YD-38 Cells from Cisplatin-induced Cell Death by Inhibiting Cytochrome c Release from Mitochondria

Affiliations
  • 1Department of Oral Biochemistry, Institute of Oral Bioscience, School of Dentistry, Jeonbuk National University, Jeonju 54907, Republic of Korea

Abstract

Cisplatin, a platinum-derived compound, has been used in treatment of various types of cancers including oral cancer. Despite its wide usage, cisplatin has multiple adverse effects affecting the systemic health of patients. Schisandrin C is a natural compound derived from Schisandra chinensis. Studies have shown its beneficial effects including antioxidant activity, hepatoprotective and renal protective actions. However, effect of schisandrin C on cisplatin-induced cytotoxicity has not been studied extensively. In this study, we examined the effect of schisandrin C treatment on YD-38 oral squamous carcinoma cell line, in combination with cisplatin treatment. Effect of schisandrin C on cisplatin-induced cell death was examined by MTT assay and live and dead cell staining. Changes in apoptosis-related intracellular signal, and ROS generation were measured by immunoblot and flow cytometry. Schisandrin C showed protective effect against cisplatin-induced cell death. Schisandrin C inhibited phosphorylation of JNK, expression of Bax, cleavage of caspase 3, and release of mitochondrial cytochrome c. In contrast, expression of Bcl2 and phosphorylation of Akt were increased by schisandrin C. Schisandrin C also suppressed intracellular reactive oxygen species generation. These results suggest that schisandrin C has a protective effect against cisplatin-induced cytotoxicity and showed a potential to be used in combination with cisplatin during chemotherapy to reduce side effects.

Keyword

cisplatin; schisandrin C; apoptosis; reactive oxygen species; mitochondria
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