1. Academic Validation
  2. Evidence that arachidonate 15-lipoxygenase 2 is a negative cell cycle regulator in normal prostate epithelial cells

Evidence that arachidonate 15-lipoxygenase 2 is a negative cell cycle regulator in normal prostate epithelial cells

  • J Biol Chem. 2002 May 3;277(18):16189-201. doi: 10.1074/jbc.M111936200.
Shaohua Tang 1 Bobby Bhatia Carlos J Maldonado Peiying Yang Robert A Newman Junwei Liu Dhyan Chandra Jeanine Traag Russell D Klein Susan M Fischer Dharam Chopra Jianjun Shen Haiyen E Zhau Leland W K Chung Dean G Tang
Affiliations

Affiliation

  • 1 Department of Carcinogenesis, the University of Texas MD Anderson Cancer Center, Science Park Research Division, Smithville, Texas 78957, USA.
Abstract

15-Lipoxygenase 2 (15-LOX2) is a recently cloned human Lipoxygenase that shows tissue-restricted expression in prostate, lung, skin, and cornea. The protein level and enzymatic activity of 15-LOX2 have been shown to be down-regulated in prostate cancers compared with normal and benign prostate tissues. The biological function of 15-LOX2 and the role of loss of 15-LOX2 expression in prostate tumorigenesis, however, remain unknown. We report the cloning and functional characterization of 15-LOX2 and its three splice variants (termed 15-LOX2sv-a, 15-LOX2sv-b, and 15-LOX2sv-c) from primary prostate epithelial cells. Western blotting with multiple primary prostate cell strains and prostate Cancer cell lines reveals that the expression of 15-LOX2 is lost in all prostate Cancer cell lines, accompanied by decreased enzymatic activity revealed by liquid chromatography/tandem mass spectrometry analyses. Further experiments show that the loss of 15-LOX2 expression results from transcriptional repression caused by mechanism(s) Other than promoter hypermethylation or histone deacetylation. Subsequent functional studies indicate the following: 1) the 15-LOX2 product, 15(S)-hydroxyeicosatetraenoic acid, inhibits prostate Cancer cell cycle progression; 2) 15-LOX2 expression in primary prostate epithelial cells is inversely correlated with cell cycle; and 3) restoration of 15-LOX2 expression in prostate Cancer cells partially inhibits cell cycle progression. Taken together, these results suggest that 15-LOX2 could be a suppressor of prostate Cancer development, which functions by restricting cell cycle progression.

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