12-Lipoxygenase and the regulation of hypoxia-inducible factor in prostate cancer cells

被引:49
作者
Krishnamoorthy, Sriram [1 ]
Jin, Rongxian [1 ]
Cai, Yinlong [1 ]
Maddipati, Krishna Rao [1 ,2 ]
Nie, Daotai [1 ]
Pages, Gilles [3 ]
Tucker, Stephanie C. [1 ]
Honn, Kenneth V. [1 ,2 ]
机构
[1] Wayne State Univ, Dept Pathol, Sch Med, Detroit, MI 48202 USA
[2] Barbara Ann Karmanos Canc Inst, Detroit, MI 48202 USA
[3] Univ Nice, CNRS, Ctr Biochim, UMR 6543, F-06108 Nice, France
关键词
12-Lipoxygenase; Hypoxia Inducible Factor-1 alpha (HIF-1 alpha); Angiogenesis; Prostate cancer; Hypoxia; PLATELET-TYPE; 12-LIPOXYGENASE; ENDOTHELIAL GROWTH-FACTOR; NF-KAPPA-B; TUMOR-GROWTH; ANGIOGENESIS; EXPRESSION; FACTOR-1-ALPHA; CARCINOMA; HIF-1; GENE;
D O I
10.1016/j.yexcr.2010.03.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
12-Lipoxygenase, an arachidonic acid metabolizing enzyme of the lipoxygenase pathway, has been implicated as a major factor in promoting prostate cancer progression and metastasis. The ability of 12-LOX to aggravate the disease was linked to its proangiogenic role. Recent studies clearly demonstrated that 12-LOX enhances the expression and secretion of the angiogenic factor, vascular endothelial growth factor (VEGF) thus providing a direct link between this enzyme and its angiogenic properties. In the present study we have investigated the relationship between 12-LOX and hypoxia inducible factor-1 alpha (HIF-1 alpha), a transcription factor involved in the regulation of VEGF expression under hypoxic conditions in solid tumors. Our findings have revealed that HIF-1 is one of the target transcription factors regulated by 12-LOX and 12(S)-HETE, in hypoxic tumor cells of the prostate. Regulation of HIF-1 alpha by 12-LOX adds to the complexity of pathways mediated by this enzyme in promoting prostate cancer angiogenesis and metastasis. We have evidence that 12-LOX increases the protein level, mRNA, and functional activity of HIF-1 alpha under hypoxic conditions, one of the mechanisms by which it upregulates VEGF secretion and activity. (c) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:1706 / 1715
页数:10
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