McEntee M F, Whelan J
Department of Pathology, College of Veterinary Medicine, Institute of Agriculture, University of Tennessee, Knoxville 37996-4542, USA.
Biomed Pharmacother. 2002 Oct;56(8):380-7. doi: 10.1016/s0753-3322(02)00254-8.
Epidemiology has implicated dietary fat in mortality associated with some of the most common forms of cancer, including those affecting the intestinal tract, breast and prostate. Polyunsaturated fatty acids, and arachidonate in particular, have been unequivocally linked to experimental colorectal carcinogenesis. Dietary, pharmacologic and genetic manipulation of tissue arachidonic acid and its conversion to bioactive lipids has provided insights into pathogenic mechanisms as well as compelling evidence to support rational preventative and therapeutic methods of disease intervention. While it is clear that conversion of arachidonate to prostaglandins and other bioactive lipids contributes significantly to tumorigenesis in the intestinal tract and other organs, it is also clear that no single metabolic pathway or lipid in this complex biochemical network is solely responsible for dietary or pharmacologic benefits evident in epidemiologic studies. We will review some of these data and provide a summary of our own work showing that conversion of arachidonate to prostaglandin E2 contributes significantly to tumor growth through the modulation of apoptosis and cellular proliferation.
流行病学研究表明,饮食中的脂肪与某些最常见癌症的死亡率有关,包括影响肠道、乳腺和前列腺的癌症。多不饱和脂肪酸,尤其是花生四烯酸,已被明确与实验性结直肠癌的发生相关联。对组织中花生四烯酸及其转化为生物活性脂质进行饮食、药理学和基因操作,有助于深入了解致病机制,并为支持合理的疾病预防和治疗干预方法提供了有力证据。虽然很明显花生四烯酸转化为前列腺素和其他生物活性脂质在肠道和其他器官的肿瘤发生中起重要作用,但同样明显的是,在这个复杂的生化网络中,没有单一的代谢途径或脂质能单独对流行病学研究中明显的饮食或药理学益处负责。我们将回顾其中一些数据,并总结我们自己的工作,表明花生四烯酸转化为前列腺素E2通过调节细胞凋亡和细胞增殖对肿瘤生长有显著贡献。