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Updated: Feb 5, 2026

Method for Novel Anti-Cancer Drug Development using Tumor Explants of Surgical Specimens
Published on: July 29, 2011
The anti-cancer efficacies of diffractaic, lobaric, and usnic acid:
Bugrahan Emsen1, Ali Aslan2, Hasan Turkez3
1Department of Biology, Kamil Özdağ Faculty of Science, Karamanoğlu Mehmetbey University, Karaman, Turkey.
Aims:
Glioblastoma multiforme (GBM) shows the most aggressive invasion among primary brain tumors. In spite of the standard therapy methods such as surgery, radiotherapy, and chemotherapy, the mortalities are high in GBM patients owing to side effects. Some lichen secondary metabolites that have many bioactive functions exhibited anti-cancer efficacy toward many cancer types. The present study was undertaken to investigate proliferation change, oxidative status and DNA damage potentials of human U87MG-GBM, and primary rat cerebral cortex (PRCC) cells exposed to three lichen secondary metabolites.
Materials And Methods:
Different concentrations of lichen secondary metabolites including diffractaic acid (DA), lobaric acid (LA), and (+)-usnic acid (UA) were used for the treatments. PRCC cells were obtained from Sprague Dawley® rats. U87MG cell line was preferred as GBM cells.
Results:
The results showed that lactate dehydrogenase and 8-hydroxy-2'-deoxyguanosine levels increased in PRCC and U87MG cells in a clear dose-dependent manner. Inhibitory concentration 50% (IC50) values of LA, DA, and UA were calculated as 9.08, 122.26, 132.69 mg/L for PRCC cells and 5.77, 35.67, 41.55 mg/L for U87MG cells, respectively. Concentration of 10 mg/L of DA and UA demonstrated high anti-oxidant capacity on healthy PRCC cells.
Conclusions:
Overall, obtained data indicated that LA was highly toxic on GBM and PRCC cells. However, DA and then UA had high anti-oxidant capacity on PRCC cells. These results suggest that further studies that will be held on LA may play a critical role in GBM treatment.
Insights
Lobaric acid (LA) shows high toxicity against glioblastoma multiforme (GBM) and rat brain cells, suggesting its potential for GBM treatment. Diffractaic acid (DA) and (+)-usnic acid (UA) exhibit antioxidant properties in healthy brain cells.
Area of Science:
- Biochemistry
- Pharmacology
- Neuroscience
Background:
- Glioblastoma multiforme (GBM) is an aggressive primary brain tumor with high mortality despite standard treatments.
- Lichen secondary metabolites possess diverse bioactive functions, including demonstrated anti-cancer efficacy against various cancer types.
- Standard GBM therapies often result in significant side effects, necessitating the exploration of novel therapeutic agents.
Purpose of the Study:
- To investigate the effects of three lichen secondary metabolites—diffractaic acid (DA), lobaric acid (LA), and (+)-usnic acid (UA)—on glioblastoma multiforme (GBM) and primary rat cerebral cortex (PRCC) cells.
- To evaluate the impact of these metabolites on cell proliferation, oxidative status, and DNA damage.
- To determine the potential of these natural compounds as therapeutic agents for GBM.
Main Methods:
- Human U87MG glioblastoma cells and primary rat cerebral cortex (PRCC) cells were treated with varying concentrations of DA, LA, and UA.
- Cellular responses including lactate dehydrogenase release and 8-hydroxy-2'-deoxyguanosine levels were measured to assess toxicity and DNA damage.
- Inhibitory concentration 50% (IC50) values were calculated for each metabolite against both cell types.
Main Results:
- Lactate dehydrogenase and 8-hydroxy-2'-deoxyguanosine levels increased in a dose-dependent manner in both PRCC and U87MG cells upon exposure to the metabolites.
- Lobaric acid (LA) exhibited the lowest IC50 values (5.77 mg/L for U87MG, 9.08 mg/L for PRCC), indicating high toxicity.
- Diffractaic acid (DA) and (+)-usnic acid (UA) demonstrated significant antioxidant capacity in healthy PRCC cells at a concentration of 10 mg/L.
Conclusions:
- Lobaric acid (LA) displays potent cytotoxicity against both GBM and normal brain cells, highlighting its potential as a GBM therapeutic agent.
- Diffractaic acid (DA) and (+)-usnic acid (UA) possess antioxidant properties beneficial for healthy brain cells.
- Further research into lobaric acid (LA) is warranted for its potential role in future glioblastoma multiforme treatments.
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