Cytotoxic effects of natural and semisynthetic cucurbitacins on lung cancer cell line A549

Invest New Drugs. 2016 Apr;34(2):139-48. doi: 10.1007/s10637-015-0317-4. Epub 2016 Jan 16.

Abstract

Cucurbitacins and their derivatives are triterpenoids that are found in various plant families, and are known for their pharmacological and biological activities, including anti-cancer effects. Lung cancer represents a major public health problem, with non-small-cell lung cancer (NSCLC) being the most frequent and aggressive type of lung cancer. The objective of this work was to evaluate four cucurbitacins (CUCs) for their cytotoxic activity, effects on apoptosis induction, cell cycle progression, anti-migratory, and anti-invasive effects on the human NSCLC cell line (A549 cells). Our findings showed that these CUCs could suppress human NSCLC cell growth in vitro through their effects on the PI3Kinase and MAPK pathways, which lead to programmed cell death induction, as well as inhibition of cell migration and cell invasion. Additionally, these effects culminate in apoptosis induction and G2/M cell cycle arrest by modulating cyclin B1 expression, and in the mitigation of strategic steps of lung cancer metastasis, including migration and invasion of A549 cells. These results suggest that two natural (DDCB and CB) and two novel semisynthetic derivatives of cucurbitacin B (ACB and DBCB) could be considered as promising compounds with antitumor potential.

Keywords: Apoptosis; Cucurbitacins; Invasion; Metastasis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • A549 Cells
  • Apoptosis / drug effects*
  • Carcinoma, Non-Small-Cell Lung / enzymology
  • Carcinoma, Non-Small-Cell Lung / pathology
  • Caspases / metabolism
  • Cell Cycle Checkpoints / drug effects
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Cucurbitacins / chemistry
  • Cucurbitacins / pharmacology*
  • Cucurbitacins / therapeutic use*
  • Cyclin B1 / metabolism
  • Down-Regulation / drug effects
  • Focal Adhesion Protein-Tyrosine Kinases / metabolism
  • Humans
  • Lung Neoplasms / drug therapy*
  • Lung Neoplasms / enzymology
  • Lung Neoplasms / pathology*
  • Matrix Metalloproteinase 2 / metabolism
  • Matrix Metalloproteinase 9 / metabolism
  • Neoplasm Invasiveness
  • Phosphorylation / drug effects
  • Signal Transduction / drug effects
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Cyclin B1
  • Tumor Necrosis Factor-alpha
  • Cucurbitacins
  • Focal Adhesion Protein-Tyrosine Kinases
  • Caspases
  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 9