Cytotoxic effects of delphinidin in human osteosarcoma cellsopen access
- Authors
- Lee, Dong-Yeong; Park, Young-Jin; Hwang, Sun-Chul; Kim, Kwang-Dong; Moon, Dong-Kyu; Kim, Dong-Hee
- Issue Date
- Jan-2018
- Publisher
- TURKISH ASSOC ORTHOPAEDICS TRAUMATOLOGY
- Keywords
- Delphinidin; Cytotoxicity; Autophagy; Apoptosis; Osteosarcoma
- Citation
- ACTA ORTHOPAEDICA ET TRAUMATOLOGICA TURCICA, v.52, no.1, pp 58 - 64
- Pages
- 7
- Indexed
- SCIE
SCOPUS
- Journal Title
- ACTA ORTHOPAEDICA ET TRAUMATOLOGICA TURCICA
- Volume
- 52
- Number
- 1
- Start Page
- 58
- End Page
- 64
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/12016
- DOI
- 10.1016/j.aott.2017.11.011
- ISSN
- 1017-995X
- Abstract
- Introduction: The aim of this study was to evaluate whether delphinidin is cytoprotective or cytotoxic in osteosarcoma cell lines, and to elucidate the underlying mechanisms. Materials and methods: The present study investigated whether apoptosis or autophagy is induced by delphinidin in human osteosarcoma cell lines. Delphinidin was used as the antioxidant, along with two autophagy inhibitors: 3-methyladenine and bafilomycin A1. Cell viability and known autophagic markers, such as LC3-II expression, were evaluated. Reactive oxygen species (ROS) formation and cell cycle analysis were also investigated. Results: Delphinidin showed concentration-dependent cytotoxicity to osteosarcoma cell. Delphinidin is closely associated with apoptotic cell death mechanisms and pathways related to ROS accumulation. In addition, we observed delphinidin-induced autophagosome formation and increasing levels of LC3-II conversion. However, in spite of delphinidin induced autophagy, the cytotoxic effects induced in the osteosarcoma cells may not be operating via autophagic cell death mechanisms. Conclusions: Delphinidin compromises the cellular protective mechanisms by inhibiting autophagy, permitting ROS to accumulate and finally enhance apoptotic cell death. Our results indicate that delphinidin may play a critical role as a chemotherapeutic agent by preventing the development and progression of osteosarcoma cells. (c) 2017 Turkish Association of Orthopaedics and Traumatology. Publishing services by Elsevier B.V.
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