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.

Abstract

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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