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首页> 外文期刊>Drugs of the Future >A novel approach to anticancer therapies for prostate cancer: lipoxygenase as a new target in the treatment of prostate cancer
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A novel approach to anticancer therapies for prostate cancer: lipoxygenase as a new target in the treatment of prostate cancer

机译:前列腺癌抗癌治疗的新方法:脂氧合酶作为前列腺癌治疗的新靶标

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摘要

Prostate cancer differs from other urinary tract tumors in that it is hormone-dependent, although angiogenic factors play a significant role in the metastasis of both prostate cancer and tumors of other organs. The metabolism of arachidonic acid (AA) by either a cyclooxygenase (COX) or lipoxygenase (LOX) pathway is considered an important factor in tumor promotion. In this review, we investigated the expression of COX and LOX (5- and 12-LOX) in prostate cancer and the effects of COX and LOX inhibitors. Our findings demonstrated that cell growth and apoptosis of human prostate cancer cells are regulated by LOX pathways. Inhibiting the growth of prostate cancer cells by blocking LOX pathways was associated with induction of apoptosis. Data also support the evidence that a 5-LOX inhibitor is significantly more effective than a 12-LOX inhibitor in preventing cancer cell growth in the prostate, as the 5-LOX pathway is more closely associated with carcinogenesis than the 12-LOX pathway. Downregulation of the AA-metabo-lizing LOX enzymes therefore provides a novel approach to anticancer therapy.
机译:前列腺癌与其他泌尿道肿瘤的区别在于它是激素依赖性的,尽管血管生成因子在前列腺癌和其他器官肿瘤的转移中都起着重要作用。通过环氧合酶(COX)或脂氧合酶(LOX)途径的花生四烯酸(AA)代谢被认为是促进肿瘤的重要因素。在这篇综述中,我们研究了前列腺癌中COX和LOX(5-和12-LOX)的表达以及COX和LOX抑制剂的作用。我们的发现表明,人前列腺癌细胞的细胞生长和凋亡受到LOX途径的调节。通过阻断LOX途径来抑制前列腺癌细胞的生长与凋亡的诱导有关。数据还支持以下证据:5-LOX抑制剂在预防前列腺癌细胞生长方面比12-LOX抑制剂有效得多,这是因为5-LOX途径比12-LOX途径与致癌作用更紧密相关。因此,AA代谢型LOX酶的下调为抗癌治疗提供了一种新方法。

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