Inhibition of hepatic endothelial E-selectin expression by C-raf antisense oligonucleotides blocks colorectal carcinoma liver metastasis

Cancer Res. 2002 Oct 1;62(19):5393-8.

Abstract

Cytokine-dependent induction of E-selectin expression is mediated through cooperative signaling involving the Ras/Raf/mitogen-activated protein kinase pathway. We previously reported that metastatic tumor cells entering the hepaticcirculation rapidly induce a cytokine cascade leading to E-selectin induction (A-M. Khatib, et al., Cancer Res., 59:1356-1361, 1999).Here, we investigated the effect of a blockade of E-selectin induction on colorectal carcinoma metastasis using rodent (host)-specific C-raf antisense oligonucleotides and human colorectal carcinoma CX-1 cells. Pretreatment of hepatic endothelial cells in vitro with the antisense oligonucleotides abrogated E-selectin-dependent CX-1 adhesion. In vivo, pretreatment of nude mice with these oligonucleotides abrogated E-selectin induction in response to intrasplenic/portal inoculation of CX-1 cells, and this reduced the number of liver metastases by 86% relative to controls. The results suggest that the inhibition of tumor-induced, hepatic microvessel E-selectin expression may provide a useful strategy for the prevention of hepatic metastasis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Adhesion / drug effects
  • Colorectal Neoplasms / drug therapy
  • Colorectal Neoplasms / metabolism
  • Colorectal Neoplasms / pathology*
  • E-Selectin / biosynthesis*
  • E-Selectin / genetics
  • Endothelium / cytology
  • Endothelium / drug effects
  • Endothelium / metabolism
  • Female
  • Humans
  • Interleukin-1 / biosynthesis
  • Interleukin-1 / genetics
  • Liver / cytology
  • Liver / drug effects*
  • Liver / metabolism*
  • Liver Neoplasms, Experimental / metabolism
  • Liver Neoplasms, Experimental / prevention & control*
  • Liver Neoplasms, Experimental / secondary*
  • Mice
  • Mice, Inbred C57BL
  • Oligonucleotides, Antisense / genetics
  • Oligonucleotides, Antisense / pharmacology*
  • Proto-Oncogene Proteins c-raf / genetics*
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Rats
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Tumor Necrosis Factor-alpha / genetics
  • Xenograft Model Antitumor Assays

Substances

  • E-Selectin
  • Interleukin-1
  • Oligonucleotides, Antisense
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Proto-Oncogene Proteins c-raf