Protein kinase C involvement in aloe-emodin- and emodin-induced apoptosis in lung carcinoma cell

Br J Pharmacol. 2001 Nov;134(5):1093-103. doi: 10.1038/sj.bjp.0704342.

Abstract

1. This study demonstrated aloe-emodin- and emodin-induced apoptosis in lung carcinoma cell lines CH27 (human lung squamous carcinoma cell) and H460 (human lung non-small cell carcinoma cell). Aloe-emodin- and emodin-induced apoptosis was characterized by nuclear morphological changes and DNA fragmentation. 2. During apoptosis, an increase in cytochrome c of cytosolic fraction and activation of caspase-3, identified by the cleavage of its proform, were observed. 3. To elucidate whether the expression of protein kinase C (PKC) isozymes are involved in aloe-emodin- and emodin-induced apoptosis, this study examined the changes of PKC isozymes by Western blotting techniques during aloe-emodin- and emodin-induced apoptosis. 4. The expression of PKC isozymes involved in aloe-emodin- and emodin-induced apoptosis of CH27 and H460 cells. In this study, aloe-emodin and emodin induced the changes of each of PKC isozymes in CH27 and H460 cells. 5. The decrease in the expression of PKC delta and epsilon may play a critical role in aloe-emodin- and emodin-induced apoptosis in CH27 and H460 cells. 6. The present study also demonstrated that PKC stimulation occurs at a site downstream of caspase-3 in the emodin-mediated apoptotic pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anthraquinones
  • Antineoplastic Agents / pharmacology*
  • Apoptosis / drug effects*
  • Blotting, Western
  • Caspase 3
  • Caspases / drug effects
  • Caspases / metabolism
  • Cell Survival / drug effects
  • Cytochrome c Group / drug effects
  • Cytochrome c Group / metabolism
  • DNA / drug effects
  • DNA / genetics
  • DNA / metabolism
  • DNA Fragmentation / drug effects
  • Dose-Response Relationship, Drug
  • Emodin / analogs & derivatives*
  • Emodin / pharmacology*
  • Enzyme Activation / drug effects
  • Enzyme Inhibitors / pharmacology*
  • Flow Cytometry
  • Humans
  • Isoenzymes / metabolism
  • Lung Neoplasms / metabolism
  • Lung Neoplasms / pathology
  • Lung Neoplasms / prevention & control
  • Oligopeptides / pharmacology
  • Protein Kinase C / metabolism*
  • Time Factors
  • Tumor Cells, Cultured / drug effects
  • Tumor Cells, Cultured / enzymology

Substances

  • Anthraquinones
  • Antineoplastic Agents
  • Cytochrome c Group
  • Enzyme Inhibitors
  • Isoenzymes
  • Oligopeptides
  • acetyl-aspartyl-glutamyl-valyl-aspartal
  • aloe emodin anthrone
  • DNA
  • aloe emodin
  • Protein Kinase C
  • CASP3 protein, human
  • Caspase 3
  • Caspases
  • Emodin