4.1 Article

Evaluation of the biological activities of olivetoric acid, a lichen-derived molecule, in human hepatocellular carcinoma cells

Journal

RENDICONTI LINCEI-SCIENZE FISICHE E NATURALI
Volume 32, Issue 1, Pages 135-148

Publisher

SPRINGER-VERLAG ITALIA SRL
DOI: 10.1007/s12210-021-00976-4

Keywords

8-OH-dG; Active ingredient; Apoptosis; Lactate dehydrogenase; Necrosis; qRT-PCR

Funding

  1. Scientific and Technological Research Council of Turkey (TUBITAK) [117Z632]

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The study tested the anticancer activity and side effects level of olivetoric acid (OA) from Pseudevernia furfuracea in human hepatocellular carcinoma cells and non-tumoral liver cells. Results showed that OA had a higher rate of apoptotic effects on HepG2 cells, induced oxidative stress and DNA damage, while significantly increased total antioxidant capacity on THLE2 cells.
Many lichen secondary metabolites contributed to the field of pharmacology as an active ingredient of different drugs for years. In the present study, we aimed to test the anticancer activity of olivetoric acid (OA), which we isolated from Pseudevernia furfuracea (L.) Zopf in human hepatocellular carcinoma cells (HepG2). In addition, we used non-tumoral human liver cells (THLE2) to test the level of side effects of OA in vitro. For this purpose, cytotoxic (apoptotic and necrotic), oxidant, genotoxic activities and expression levels of apoptotic genes caused by different concentrations (12.5-400 mg/L) of OA were tested on both cells. Flow cytometric and cytotoxicity tests (MTT and LDH) revealed that OA (100-400 mg/L) had a higher rate of apoptotic effects on HepG2 cells compared to THLE2. Total oxidative stress and oxidative DNA damage levels caused by all concentrations of OA on HepG2 cells was significantly (p < 0.05) higher compared to negative control. Trials with concentrations of 100-400 mg/L significantly (p < 0.05) increased total antioxidant capacity on THLE2 cells compared to the control group. As a result, based on human hepatocellular carcinoma, it is hoped that OA may contribute to the combined or alternative treatment process.

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