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Aberrant Activation of Arachidonic Acid and Eicosanoid Pathways-Targets for Treating Prostate Cancer

机译:花生四烯酸和类花生酸途径异常激活靶点治疗前列腺癌

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摘要

Eicosanoids have been the major therapeutic targets in rheumatoid arthritis and other degenerative diseases where inflammation is involved. In the past decade, the biological significance of eicosanoids and their potential as therapeutic targets in cancer have also been recognized and is now a focal area of research in many laboratories. Recently, phospholipase A2 (PLA2), the enzyme responsible for arachidonic acid supply to eicosanoid-producing enzymes has attracted attention. It has been proposed that PLA2 inhibition can yield a better therapeutic outcome than inhibition of individual eicosanoid-producing enzymes. In this article, we focus on the rationale for targeting arachidonic acideicosanoid pathways as well as evaluate the recent patents that identify inhibitors of the PLA2 family of enzymes.
机译:类花生酸一直是类风湿关节炎和其他涉及炎症的退化性疾病的主要治疗靶标。在过去的十年中,类花生酸的生物学意义及其作为癌症治疗靶标的潜力也得到了认可,现在已成为许多实验室研究的重点领域。最近,磷脂酶A2(PLA2)是负责花生四烯酸向类二十烷酸生产酶供应的酶,已引起人们的关注。已经提出,与抑制单个类花生酸产生的酶相比,抑制PLA2可产生更好的治疗效果。在本文中,我们将重点放在针对花生四烯酸酸类二十烷酸途径的理论基础上,并评估鉴定了PLA2酶抑制剂的最新专利。

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