Inhibition of heme oxygenase-1 interferes with the transforming activity of the Kaposi sarcoma herpesvirus-encoded G protein-coupled receptor

J Biol Chem. 2006 Apr 21;281(16):11332-46. doi: 10.1074/jbc.M512199200. Epub 2006 Feb 13.

Abstract

Heme oxygenase-1 (HO-1), the inducible enzyme responsible for the rate-limiting step in the heme catabolism, is expressed in AIDS-Kaposi sarcoma (KS) lesions. Its expression is up-regulated by the Kaposi sarcoma-associated herpesvirus (KSHV) in endothelial cells, but the mechanisms underlying KSHV-induced HO-1 expression are still unknown. In this study we investigated whether the oncogenic G protein-coupled receptor (KSHV-GPCR or vGPCR), one of the key KSHV genes involved in KS development, activated HO-1 expression. Here we show that vGPCR induces HO-1 mRNA and protein levels in fibroblasts and endothelial cells. Moreover, targeted knock-down gene expression of HO-1 by small hairpin RNA and chemical inhibition of HO-1 enzymatic activity by tin protoporphyrin IX (SnPP), impaired vGPCR-induced survival, proliferation, transformation, and vascular endothelial growth factor (VEGF)-A expression. vGPCR-expressing cells implanted in the dorsal flank of nude mice developed tumors with elevated HO-1 expression and activity. Chronic administration of SnPP to the implanted mice, under conditions that effectively blocked HO-1 activity and VEGF-A expression in the transplanted cells, strikingly reduced tumor growth, without apparent side effects. On the contrary, administration of the HO-1 inducer cobalt protoporphyrin (CoPP) further enhanced vGPCR-induced tumor growth. These data postulate HO-1 as an important mediator of vGPCR-induced tumor growth and suggest that inhibition of intratumoral HO-1 activity by SnPP may be a potential therapeutic strategy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Annexin A5 / pharmacology
  • Apoptosis
  • Blotting, Western
  • Cell Proliferation
  • Cell Survival
  • Culture Media, Serum-Free / metabolism
  • DNA / metabolism
  • Dose-Response Relationship, Drug
  • Endothelial Cells / metabolism
  • Enzyme Inhibitors / pharmacology*
  • Fibroblasts / metabolism
  • Fluorescent Antibody Technique, Indirect
  • Genes, Reporter
  • Heme / chemistry
  • Heme Oxygenase (Decyclizing) / metabolism
  • Heme Oxygenase-1 / antagonists & inhibitors*
  • Heme Oxygenase-1 / metabolism
  • Herpesvirus 8, Human / metabolism*
  • Immunohistochemistry
  • Luciferases / metabolism
  • Metalloporphyrins / metabolism
  • Mice
  • Mice, Nude
  • Models, Biological
  • NIH 3T3 Cells
  • Neoplasm Transplantation
  • Neoplasms / metabolism
  • Promoter Regions, Genetic
  • Protoporphyrins / chemistry
  • Protoporphyrins / metabolism
  • RNA / metabolism
  • RNA, Messenger / metabolism
  • Receptors, G-Protein-Coupled / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors
  • Transfection
  • Up-Regulation
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • Annexin A5
  • Culture Media, Serum-Free
  • Enzyme Inhibitors
  • Metalloporphyrins
  • Protoporphyrins
  • RNA, Messenger
  • Receptors, G-Protein-Coupled
  • Vascular Endothelial Growth Factor A
  • Heme
  • RNA
  • cobaltiprotoporphyrin
  • DNA
  • tin protoporphyrin IX
  • Luciferases
  • Heme Oxygenase (Decyclizing)
  • Heme Oxygenase-1