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Hypoxia-inducible factor 1-dependent expression of platelet-derived growth factor B promotes lymphatic metastasis of hypoxic breast cancer cells

Proc Natl Acad Sci U S A. 2012 Oct 2;109(40):E2707-16. doi: 10.1073/pnas.1214019109. Epub 2012 Sep 10.

Abstract

Lymphatic dissemination from the primary tumor is a major mechanism by which breast cancer cells access the systemic circulation, resulting in distant metastasis and mortality. Numerous studies link activation of hypoxia-inducible factor 1 (HIF-1) with tumor angiogenesis, metastasis, and patient mortality. However, the role of HIF-1 in lymphatic dissemination is poorly understood. In this study, we show that HIF-1 promotes lymphatic metastasis of breast cancer by direct transactivation of the gene encoding platelet-derived growth factor B (PDGF-B), which has proliferative and chemotactic effects on lymphatic endothelial cells. Lymphangiogenesis and lymphatic metastasis in mice bearing human breast cancer orthografts were blocked by administration of the HIF-1 inhibitor digoxin or the tyrosine kinase inhibitor imatinib. Immunohistochemical analysis of human breast cancer biopsies demonstrated colocalization of HIF-1α and PDGF-B, which were correlated with lymphatic vessel area and histological grade. Taken together, these data provide experimental support for breast cancer clinical trials targeting HIF-1 and PDGF-B.

MeSH terms

  • Benzamides
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / physiopathology*
  • Cell Hypoxia / physiology
  • Cell Line, Tumor
  • Chromatin Immunoprecipitation
  • Digoxin / pharmacology
  • Female
  • Humans
  • Hypoxia-Inducible Factor 1 / antagonists & inhibitors
  • Hypoxia-Inducible Factor 1 / physiology*
  • Imatinib Mesylate
  • Immunoblotting
  • Immunohistochemistry
  • Luciferases
  • Lymphangiogenesis / drug effects
  • Lymphatic Metastasis / physiopathology*
  • Piperazines / pharmacology
  • Proto-Oncogene Proteins c-sis / metabolism*
  • Pyrimidines / pharmacology
  • RNA, Small Interfering / metabolism
  • Transcriptional Activation / drug effects
  • Transcriptional Activation / physiology*

Substances

  • Benzamides
  • Hypoxia-Inducible Factor 1
  • Piperazines
  • Proto-Oncogene Proteins c-sis
  • Pyrimidines
  • RNA, Small Interfering
  • Digoxin
  • Imatinib Mesylate
  • Luciferases