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논문 기본 정보

자료유형
학술저널
저자정보
Seo Ji-Hye (Department of Dental Pharmacology School of Dentistry Jeonbuk National University Jeonju 54896 Repu) Yoon Goo (Department of Pharmacy College of Pharmacy Mokpo National University Muan 58554 Republic of Korea) Park Seryoung (Disease Target Structure Research Center Korea Research Institute of Bioscience and Biotechnology () Shim Jung-Hyun (Department of Pharmacy College of Pharmacy and Natural Medicine Research Institute Mokpo National U) Chae Jung-Il (Department of Dental Pharmacology School of Dentistry Jeonbuk National University Jeonju 54896 Repu) Jeon Young-Joo (Disease Target Structure Research Center Korea Research Institute of Bioscience and Biotechnology ()
저널정보
한국미생물생명공학회 Journal of Microbiology and Biotechnology Journal of Microbiology and Biotechnology 제32권 제9호
발행연도
2022.9
수록면
1,103 - 1,109 (7page)
DOI
10.4014/jmb.2207.07012

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Deoxypodophyllotoxin (DPT), a naturally occurring flavonolignan, possesses several pharmacological properties, including anticancer property. However, the mechanisms underlying DPT mode of action in oral squamous cell carcinoma (OSCC) remain unknown. This study aimed to investigate the anticancer effects of DPT on OSCC and the underlying mechanisms. Results of the MTT assay revealed that DPT significantly reduced the cell viability in a time- and dose-dependent manner. Flow cytometry analysis revealed that DPT induces apoptosis in OSCC cells in a dosedependent manner. Moreover, DPT enhanced the production of mitochondrial reactive oxygen species (ROS) in OSCC cells. Mechanistically, DPT induced apoptosis in OSCC cells by suppressing the PI3K/AKT signaling pathway while activating the p38 MAPK signaling to regulate the expression of apoptotic proteins. Treatment with SC79, an AKT activator, reversed the effects of DPT on AKT signaling in OSCC cells. Taken together, these results provide the basis for the use of DPT in combination with conventional chemotherapy for the treatment of oral cancer.

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