Inhibition of carcinogenesis in transgenic mouse models over-expressing 15-lipoxygenase in the vascular wall under the control of murine preproendothelin-1 promoter

Dror Harats, Dikla Ben-Shushan, Hofit Cohen, Ayelet Gonen, Iris Barshack, Iris Goldberg, Shoshana Greenberger, Israel Hodish, Ayelet Harari, Nira Varda-Bloom, Keren Levanon, Ehud Grossman, Pavlos Chaitidis, Hartmut Kühn, Aviv Shaish

Research output: Contribution to journalArticlepeer-review

38 Scopus citations

Abstract

Oxygenases are a family of enzymes that dioxygenate unsaturated fatty acids, thus initiating membrane oxidation and signaling molecule synthesis. The lipoxygenases (LOs), a family of lipid-peroxidizing enzymes that induce structural and metabolic changes in the cell in a number of pathophysiological conditions, belong to the oxygenases family. This class of enzymes has several subgroups, named 5-, 8-, 12- and 15-LOs, and these LO-isoforms are capable of oxygenating arachidonic and linoleic acid. 15-LOs were reported to play an inhibitory role in tumor angiogenesis and, consequently, they slow down carcinogenesis. It has been suggested that its anti-carcinogenic effect is conferred by promoting cell differentiation and apoptosis. Using transgenic mice that over-express 15-LO-1 in endothelial cells under the regulation of the murine preproendothelin-1 promoter, we studied its effect on tumor and metastasis growth. We found that 15-LO-1 inhibited tumor and metastasis growth in the transgenic mice in two different models of cancer (mammary gland and Lewis lung carcinoma). This inhibition was concomitant with a higher number of apoptotic cells in the metastases of the transgenic mice and with a complicated network of multiple small blood vessels. This finding targets 15-LO as a new candidate in the treatment of carcinogenesis.

Original languageEnglish
Pages (from-to)127-134
Number of pages8
JournalCancer Letters
Volume229
Issue number1
DOIs
StatePublished - 8 Nov 2005
Externally publishedYes

Keywords

  • 15-lipoxygenase
  • Angiogenesis
  • Carcinogenesis
  • Endothelial cells
  • Transgenic Mice

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