A Pre-clinical Trial Study: Anti-human Colon Cancer Effect of Thalassiolin B in vitro with Enzymes Inhibition Effects and Molecular Docking Studies

J Oleo Sci. 2022;71(2):267-276. doi: 10.5650/jos.ess21290.

Abstract

In this study, it is recorded the inhibition effect of Thalassiolin B on aldose reductase, alpha-glucosidase and alpha-amylase enzymes. In the next step, the molecular docking method was used to compare the biological activities of the Thalassiolin B molecule against enzymes formed from the assembly of proteins. In these calculations, the enzymes used are Aldose reductase, Alpha-Amylase, and Alpha-Glucosidase, respectively. After the docking method, ADME/T analysis of Thalassiolin B molecule was performed to be used as a drug in the pharmaceutical industry. In the MTT assay, the anti-human colon cancer properties of Thalassiolin B against EB, LS1034, and SW480 cell lines were investigated. The cell viability of Thalassiolin B was very low against human colon cancer cell lines without any cytotoxicity on the human normal (HUVEC) cell line. The IC50 of the Thalassiolin B against EB, LS1034, and SW480 were 483, 252, and 236 µg/mL, respectively. Thereby, the best cytotoxicity results and anti-human colon cancer potentials of our Thalassiolin B were observed in the case of the SW480 cell line. Maybe the anti-human colon cancer properties of Thalassiolin B are related to their antioxidant effects.

Keywords: Thalassiolin B; colon cancer; cytotoxicity; enzyme inhibition; molecular docking studies.

MeSH terms

  • Aldehyde Reductase / antagonists & inhibitors*
  • Antineoplastic Agents, Phytogenic*
  • Antioxidants*
  • Biological Products / pharmacology*
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Colonic Neoplasms / pathology*
  • Dose-Response Relationship, Drug
  • Drug Screening Assays, Antitumor / methods*
  • Flavonoids / pharmacology*
  • Glycoside Hydrolase Inhibitors*
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • Molecular Docking Simulation / methods*
  • alpha-Amylases / antagonists & inhibitors*
  • alpha-Glucosidases

Substances

  • Antineoplastic Agents, Phytogenic
  • Antioxidants
  • Biological Products
  • Flavonoids
  • Glycoside Hydrolase Inhibitors
  • thalassiolin B
  • Aldehyde Reductase
  • alpha-Amylases
  • alpha-Glucosidases