Klein Robert F, Allard John, Avnur Zafrira, Nikolcheva Tania, Rotstein David, Carlos Amy S, Shea Marie, Waters Ruth V, Belknap John K, Peltz Gary, Orwoll Eric S
Bone and Mineral Research Unit, Department of Medicine, School of Medicine, Oregon Health and Science University, 3181 Southwest Sam Jackson Park Road, Portland, OR 97239, USA.
Science. 2004 Jan 9;303(5655):229-32. doi: 10.1126/science.1090985.
The development of osteoporosis involves the interaction of multiple environmental and genetic factors. Through combined genetic and genomic approaches, we identified the lipoxygenase gene Alox15 as a negative regulator of peak bone mineral density in mice. Crossbreeding experiments with Alox15 knockout mice confirmed that 12/15-lipoxygenase plays a role in skeletal development. Pharmacologic inhibitors of this enzyme improved bone density and strength in two rodent models of osteoporosis. These results suggest that drugs targeting the 12/15-lipoxygenase pathway merit investigation as a therapy for osteoporosis.
骨质疏松症的发展涉及多种环境和遗传因素的相互作用。通过综合遗传和基因组学方法,我们确定脂氧合酶基因Alox15是小鼠峰值骨矿物质密度的负调节因子。与Alox15基因敲除小鼠的杂交实验证实12/15-脂氧合酶在骨骼发育中起作用。该酶的药理抑制剂在两种骨质疏松症啮齿动物模型中提高了骨密度和强度。这些结果表明,靶向12/15-脂氧合酶途径的药物作为骨质疏松症的一种治疗方法值得研究。