Genetic disruption of host nitric oxide synthase II gene impairs melanoma-induced angiogenesis and suppresses pleural effusion

Int J Cancer. 2001 Mar 1;91(5):607-11.

Abstract

Our previous study showed that genetic disruption of nitric oxide (NO) synthase II (NOS II) expression inhibits the metastatic ability of non-immunogenic B16 melanoma cells in syngeneic mice. In the present study, the mechanisms for this metastasis suppression were determined. B16-BL6 and B16-F10 murine melanoma cells were injected i.v. into syngeneic wild-type (NOS II(+/+)) and NOS II-null (NOS II(-/-)) C57BL/6 mice. Both melanoma cells produced less and smaller experimental pulmonary metastases in NOS II(-/-) mice than in NOS II(+/+) mice. Moreover, less metastatic pleural effusion was observed in NOS II(-/-) mice than in NOS II(+/+) mice. Immunohistochemical analyses indicated that absence of NOS II expression was correlated with decreased vascular endothelial growth factor expression and tumor-associated vascular formation. After activation with lipopolysaccharide and IFN-gamma, neither melanoma cell line produced detectable levels of NO. Our data demonstrate that tumor-induced expression of host NOS II enhances melanoma metastasis and pleural effusion, at least in part, through regulation of vascular formation and vascular permeability.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Endothelial Growth Factors / biosynthesis
  • Enzyme-Linked Immunosorbent Assay
  • Genes, p53 / genetics
  • Immunohistochemistry
  • Interferon-gamma / metabolism
  • Lipopolysaccharides / metabolism
  • Lymphokines / biosynthesis
  • Melanoma / genetics*
  • Melanoma / metabolism
  • Melanoma, Experimental
  • Mice
  • Mice, Inbred C57BL
  • Mice, Mutant Strains
  • Neoplasm Metastasis
  • Neoplasm Transplantation
  • Neovascularization, Pathologic*
  • Nitric Oxide / biosynthesis
  • Nitric Oxide Synthase / genetics*
  • Nitric Oxide Synthase / physiology*
  • Nitric Oxide Synthase Type II
  • Nitrites / metabolism
  • Pleural Effusion / genetics*
  • RNA, Messenger / metabolism
  • Tumor Cells, Cultured
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors

Substances

  • Endothelial Growth Factors
  • Lipopolysaccharides
  • Lymphokines
  • Nitrites
  • RNA, Messenger
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors
  • Nitric Oxide
  • Interferon-gamma
  • Nitric Oxide Synthase
  • Nitric Oxide Synthase Type II