Natural anthraquinone compound emodin as a novel inhibitor of aurora A kinase: A pilot study

Chem Biol Drug Des. 2022 Jan;99(1):126-135. doi: 10.1111/cbdd.13938. Epub 2021 Sep 6.

Abstract

Aurora kinase A (AURKA) carries out an essential role in proliferation and involves in cisplatin resistance in various cancer cells. Overexpression of AURKA is associated with the poor prognosis of cancer patients. Thus, AURKA has been considered as a target for cancer therapy. Developing AURKA inhibitors became an important issue in cancer therapy. A natural compound emodin mainly extracted from rhubarbs possesses anti-cancer properties. However, the effect of emodin on AURKA has never been investigated. In the present study, molecular docking analysis indicated that emodin interacts with AURKA protein active site. We also found nine emodin analogues from Key Organic database by using ChemBioFinder software. Among that, one analogue 8L-902 showed a similar anti-cancer effect as emodin. The bindings of emodin and 8L-902 on AURKA protein were confirmed by cellular thermal shift assay. Furthermore, emodin inhibited the AURKA kinase activity in vitro and enhanced the cisplatin-DNA adduct level in a resistant ovarian cancer cell line. It seems that emodin may have the potential to inhibit cancer cell growth and enhance cisplatin therapy in cancer with resistance. Collectively, our finding reveals a novel AURKA inhibitor, emodin, which may be vulnerable to ovarian cancer therapy in the future.

Keywords: Aurora kinase A; analogue; emodin; inhibitor; ovarian cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anthraquinones / chemistry*
  • Anthraquinones / metabolism
  • Anthraquinones / pharmacology
  • Aurora Kinase A / antagonists & inhibitors*
  • Aurora Kinase A / metabolism
  • Binding Sites
  • Catalytic Domain
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Cisplatin / analysis
  • Cisplatin / chemistry
  • Cisplatin / pharmacology
  • DNA Adducts / analysis
  • Databases, Chemical
  • Emodin / analogs & derivatives*
  • Emodin / metabolism
  • Emodin / pharmacology
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Molecular Docking Simulation
  • Pilot Projects
  • Protein Binding
  • Protein Kinase Inhibitors / chemistry*
  • Protein Kinase Inhibitors / metabolism
  • Protein Kinase Inhibitors / pharmacology
  • Temperature

Substances

  • Anthraquinones
  • DNA Adducts
  • Protein Kinase Inhibitors
  • cisplatin-DNA adduct
  • Aurora Kinase A
  • Emodin
  • Cisplatin