Bioactive compounds from Lactarius deterrimus interfere with the invasive potential of gastric cancer cells

  • Kamila Król Department of Cell Biology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Kraków, Poland
  • Maciej Pudełek Department of Cell Biology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Kraków, Poland
  • Gracjana Krzysiek-Mączka Department of Physiology, Faculty of Medicine, Jagiellonian University Medical College, Kraków, Poland
  • Mateusz Wierdak 2nd Department of General Surgery, Faculty of Medicine, Jagiellonian University Medical College, Kraków, Poland
  • Bożena Muszyńska Jagiellonian University Medical College, Faculty of Pharmacy, Department of Pharmaceutical Botany, Kraków, Poland
  • Katarzyna Sułkowska-Ziaja Jagiellonian University Medical College, Faculty of Pharmacy, Department of Pharmaceutical Botany, Kraków, Poland
  • Agata Krakowska Jagiellonian University Medical College, Faculty of Pharmacy, Department of Inorganic and Analytical Chemistry, Kraków, Poland
  • Damian Ryszawy Department of Cell Biology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Kraków, Poland
  • Jarosław Czyż Department of Cell Biology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Kraków, Poland

Abstract

Stomach cancer is the 4th most common cancer diagnosed worldwide. Despite intensive research on its etiopathology, its treatment strategies have not changed in the last 50 years. Mushrooms have recently attracted much attention as the source of bioactive compounds that can potentially complement cancer therapies. Here, we extracted a phenolic fraction from Lactarius deterrimus and analyzed its composition and bioactivity against the gastric cancer (AGS) cells. The complexity of L. deterrimus compounds was revealed by an HPLC assay, and was accompanied by cytostatic, cytotoxic and anti-invasive effects of the L. deterrimus extract (LDE). These are illustrated by inhibition of the AGS cells’ proliferation, metabolic activity and motility, and by induction of the cytoskeleton rearrangements. Apparently, these effects are exerted via activation of intracellular oxidative stress and decreased ATP production in AGS cells that could not be compensated by induction of autophagy. Less severe LDE effects were seen on physiology of normal gastric fibroblasts; however, inhibition of their motility indicates that LDE can interfere with gastric cancer development via an effect on stromal cells. Along with the observed synergy of LDE and cisplatin/5-fluorouracil effects on AGS cells, our data show the potential of LDE for supplementation of the gastric cancer therapy.

Published
2021-11-14
Section
Articles