Chemopreventive effects of standardized ethanol extract from the aerial parts of Artemisia princeps Pampanini cv. Sajabal via NF-κB inactivation on colitis-associated colon tumorigenesis in mice

Food Chem Toxicol. 2015 Jan:75:14-23. doi: 10.1016/j.fct.2014.11.007. Epub 2014 Nov 13.

Abstract

Chronic inflammation is an underlying risk factor of colon cancer, and NF-κB plays a critical role in the development of inflammation-associated colon cancer in an AOM/DSS mouse model. The aim of this study was to determine whether the standardized ethanol extract obtained from the aerial parts of Artemisia princeps Pampanini cv. Sajabal (EAPP) is effective at preventing inflammation-associated colon cancer, and if so, to identify the signaling pathways involved. In the present study, protective efficacy of EAPP on tumor formation and the infiltrations of monocytes and macrophages in colons of an AOM/DSS mouse model were evaluated. It was found that colitis and tumor burdens showed statistically meaningful improvements after EAPP administration. Furthermore, these improvements were accompanied by a reduction in NF-κB activity and in the levels of NF-κB-dependent pro-survival proteins, that is, survivin, cFLIP, XIAP, and Bcl-2. In vitro, EAPP significantly reduced NF-κB activation and the levels of IL-1β and IL-8 mRNA and pro-survival proteins in HT-29 and HCT-116 colon cancer cells. Furthermore, EAPP caused caspase-dependent apoptosis. Based on these results, the authors suggest EAPP suppresses inflammatory responses and induces apoptosis partly via NF-κB inactivation, and that EAPP could be useful for the prevention of colitis-associated tumorigenesis.

Keywords: AOM/DSS-induced colon cancer; Apoptosis; Artemisia princeps Pampanini cv. Sajabal; Caspase; Nuclear factor-kappaB.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anticarcinogenic Agents / pharmacology*
  • Apoptosis / drug effects
  • Artemisia / chemistry*
  • Carcinogenesis / drug effects
  • Colitis / complications*
  • Colonic Neoplasms / etiology
  • Colonic Neoplasms / prevention & control*
  • HCT116 Cells
  • HT29 Cells
  • Humans
  • Interleukin-1beta / genetics
  • Interleukin-1beta / metabolism
  • Interleukin-8 / genetics
  • Interleukin-8 / metabolism
  • Macrophages / drug effects
  • Male
  • Mice
  • Mice, Inbred ICR
  • Monocytes / drug effects
  • NF-kappa B / antagonists & inhibitors
  • NF-kappa B / metabolism*
  • Plant Components, Aerial / chemistry
  • Plant Extracts / pharmacology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism

Substances

  • Anticarcinogenic Agents
  • Interleukin-1beta
  • Interleukin-8
  • NF-kappa B
  • Plant Extracts
  • RNA, Messenger