Ilimaquinone Induces Apoptosis and Autophagy in Human Oral Squamous Cell Carcinoma Cells.
Cheng-Wen LinLi-Yuan BaiJui-Hsin SuChang-Fang ChiuWei-Yu LinWei-Ting HuangMing-Cheng ShihYu-Ting HuangJing-Lan HuJing-Ru WengPublished in: Biomedicines (2020)
In this study, the anti-tumor activity of ilimaquinone (IQ), a sesquiterpene quinone isolated from marine sponge Halichondria sp., in oral squamous cell carcinoma (OSCC) cells, was investigated. IQ suppressed the viability of the OSCC cell lines SCC4 and SCC2095 with IC50 values of 7.5 and 8.5 μM, respectively. Flow cytometric analysis demonstrated that IQ induced caspase-dependent apoptosis in SCC4 cells and modulated the expression of several cell growth-related gene products, including Akt, p38, Mcl-1, and p53. Notably, p53 knockdown caused higher resistance to IQ's anti-tumor activity. In addition, IQ increased reactive oxygen species generation, which was partially reversed by the addition of antioxidants. Furthermore, it triggered autophagy, as evidenced by acidic organelle formation and LC3B-II and Atg5 expression in SCC4 cells. Pretreatment with the autophagy inhibitor 3-methyladenine or chloroquine partially decreased IQ-induced apoptosis, suggesting that IQ induced protective autophagy. In summary, IQ has potential to be used in OSCC therapy.
Keyphrases
- induced apoptosis
- endoplasmic reticulum stress
- signaling pathway
- oxidative stress
- cell death
- cell cycle arrest
- diabetic rats
- poor prognosis
- pi k akt
- endothelial cells
- reactive oxygen species
- squamous cell
- high glucose
- drug induced
- stem cells
- binding protein
- mesenchymal stem cells
- gene expression
- long non coding rna
- genome wide
- bone marrow