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Functional changes in murine mammary cancer cells elicited by CoCl2-induced hypoxia.

Abstract
Low O(2) levels in solid tumors are associated with increase in hypoxia-inducible factor 1alpha (HIF-1alpha). The present study examines functional changes involved in adaptation to hypoxia of the LMM3 mammary tumor cell line, using CoCl(2) as hypoxic mimetic. Our results showed that LMM3 cells were not only tolerant to 150 microM CoCl(2) but they can overgrowth in vitro respect to untreated cells. Hypoxia inhibited cell invasion, migration, MMP-9 activity and NO levels. Macrophage cytotoxicity augmented under hypoxia but was blunted by conditioned media from tumor cells. In vivo tumorigenicity of CoCl(2)-treated cells was greater than controls. Our results show stabilization of HIF-1alpha in LMM3 cells under CoCl(2) and functional changes associated with enhanced cell survival and growth but not with tumor dissemination.
AuthorsXimena Borenstein, Gabriel L Fiszman, Ada Blidner, Silvia I Vanzulli, María A Jasnis
JournalNitric oxide : biology and chemistry (Nitric Oxide) Vol. 23 Issue 3 Pg. 234-41 (Nov 01 2010) ISSN: 1089-8611 [Electronic] United States
PMID20633694 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightPublished by Elsevier Inc.
Chemical References
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Tumor Necrosis Factor-alpha
  • Nitric Oxide
  • Cobalt
  • cobaltous chloride
Topics
  • Animals
  • Cell Movement (drug effects)
  • Cell Proliferation (drug effects)
  • Cell Survival (drug effects)
  • Cobalt (pharmacology)
  • Dose-Response Relationship, Drug
  • Hypoxia
  • Hypoxia-Inducible Factor 1, alpha Subunit (biosynthesis)
  • Macrophages (drug effects)
  • Mice
  • Mice, Inbred BALB C
  • Nitric Oxide (biosynthesis)
  • Structure-Activity Relationship
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha (biosynthesis)

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