15,16-Dihydrotanshinone I-induced apoptosis in human colorectal cancer cells: involvement of ATF3

Anticancer Res. 2013 Aug;33(8):3225-31.

Abstract

15,16-Dihydrotanshinone I (DHTS) is a component of the traditional Chinese medicinal plant Salvia miltiorrhiza Bunge. In this study, DHTS at as low as 2.5 μg/ml concentration significantly inhibited proliferation of human benign (SW480) and malignant (SW620) colorectal cancer cells, as shown by 3-(4,5)-dimethylthiahiazo (-z-y1)-3,5-diphenytetrazoliumromide (MTT) and flow cytometric analysis. Activating transcription factor (ATF)-3, a basic leucine zipper-type transcription factor, was found to be predominantly up-regulated in DHTS-treated SW480 and SW620 cells. The up-regulation of ATF3 was blocked by a c-JUN N-terminal kinase (JNK) or p38 inhibitor. Overexpression of ATF3 resulted in a significant augmentation of DHTS-induced apoptosis of SW480 cells, but resistance to DHTS-induced apoptosis of SW620 cells. These results suggest that DHTS has a strong therapeutic or preventive potential against cancer. In addition, ATF3 has a dual role in DHTS-induced apoptosis, depending on the degree of malignancy of colorectal cancer.

Keywords: 15,16-Dihydrotanshinone I; SW420 cells; SW480; SW620; activating transcription factor-3; colorectal cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Activating Transcription Factor 3 / metabolism*
  • Adenocarcinoma / metabolism
  • Adenocarcinoma / pathology
  • Apoptosis / drug effects*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Colorectal Neoplasms / enzymology
  • Colorectal Neoplasms / metabolism*
  • Colorectal Neoplasms / pathology*
  • Drug Screening Assays, Antitumor
  • Furans
  • Humans
  • MAP Kinase Signaling System / drug effects
  • Mitogen-Activated Protein Kinases / metabolism
  • Neoplasm Metastasis
  • Phenanthrenes / pharmacology*
  • Phosphorylation / drug effects
  • Quinones

Substances

  • ATF3 protein, human
  • Activating Transcription Factor 3
  • Furans
  • Phenanthrenes
  • Quinones
  • dihydrotanshinone I
  • Mitogen-Activated Protein Kinases