Ursolic acid inhibits the growth of colon cancer-initiating cells by targeting STAT3

Anticancer Res. 2013 Oct;33(10):4279-84.

Abstract

Background: We have previously reported Signal Transducer and Activator of Transcription 3 (STAT3) to be constitutively activated in aldehyde dehydrogenase (ALDH)(+)/cluster of differentiation-133 (CD133)(+) colon cancer-initiating cells. In the present study we tested the efficacy of inhibiting STAT3 signaling in human colon cancer-initiating cells by ursolic acid (UA), which exists widely in fruits and herbs.

Results: Our data demonstrated that UA inhibited STAT3 phosphorylation, and induced caspase-3 cleavage of ALDH(+)/CD133(+) colon cancer-initiating cells. UA also reduced cell viability and inhibited tumor sphere formation of colon cancer-initiating cells, more potently than two other natural compounds, resveratrol and capsaicin. UA also inhibited the activation of STAT3 induced by interleukin-6 in DLD-1 colon cancer cells. Furthermore, daily administration of UA suppressed HCT116 tumor growth in mice in vivo.

Conclusion: Our results suggest STAT3 to be a target for colon cancer prevention. UA, a dietary agent, might offer an effective approach for colorectal carcinoma prevention by inhibiting persistently activated STAT3 in cancer stem cells.

Keywords: STAT3; Ursolic acid; cancer-initiating cells; colon cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Caspase 3 / metabolism
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Colonic Neoplasms / drug therapy*
  • Colonic Neoplasms / pathology
  • Enzyme Activation / drug effects
  • Female
  • HCT116 Cells
  • HT29 Cells
  • Humans
  • Interleukin-6 / physiology
  • Mice
  • Mice, Nude
  • Neoplastic Stem Cells / drug effects
  • Neoplastic Stem Cells / physiology*
  • Phosphorylation
  • Protein Processing, Post-Translational / drug effects*
  • STAT3 Transcription Factor / metabolism*
  • Spheroids, Cellular / drug effects
  • Triterpenes / pharmacology*
  • Tumor Burden / drug effects
  • Ursolic Acid
  • Xenograft Model Antitumor Assays

Substances

  • Antineoplastic Agents, Phytogenic
  • Interleukin-6
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • Triterpenes
  • CASP3 protein, human
  • Caspase 3