Proteomics Analysis for Identification of Potential Cell Signaling Pathways and Protein Targets of Actions of Atractylodin and β-Eudesmol Against Cholangiocarcinoma

Asian Pac J Cancer Prev. 2020 Mar 1;21(3):621-628. doi: 10.31557/APJCP.2020.21.3.621.

Abstract

Objective: The study aimed to identify potential cell signaling pathways and protein targets of actions of atractylodin and β-eudesmol in cholangiocarcinoma, the two active compounds isolated from Atracylodes lancea using proteomics approach.

Method: The cholangiocarcinoma cell line, CL-6, was treated with each compound for 3 and 6 hours, and the proteins from both intra- and extracellular components were extracted. LC-MS/MS was applied following the separation of the extract proteins by SDS-PAGE and digestion with trypsin. Signaling pathways and protein expression were analyzed by MASCOT and STITCH software.

Results: A total of 4,323 and 4,318 proteins were identified from intra- and extracellular components, respectively. Six and 4 intracellular proteins were linked with the signaling pathways (apoptosis, cell cycle control, and PI3K-AKT) of atractylodin and β-eudesmol, respectively. Four and 3 extracellular proteins were linked with the signaling pathways (NF-κB and PI3K-AKT) of atractylodin and β-eudesmol, respectively.

Conclusion: In conclusion, a total of 17 proteins associated with four cell signaling pathways that could be potential molecular targets of anticholangiocarcinoma action of atractylodin and β-eudesmol were identified through the application of proteomics approach.

Keywords: Atractylodin; cholangiocarcinoma; proteomics; signaling pathway; β-eudesmol.

MeSH terms

  • Apoptosis
  • Bile Duct Neoplasms / metabolism*
  • Bile Duct Neoplasms / pathology
  • Cell Cycle
  • Cell Line, Tumor
  • Cholangiocarcinoma / metabolism*
  • Furans / metabolism*
  • Humans
  • Proteomics
  • Sesquiterpenes, Eudesmane / metabolism*
  • Signal Transduction*

Substances

  • Furans
  • Sesquiterpenes, Eudesmane
  • beta-eudesmol
  • atractylodin