Targeting arachidonic acid pathway by natural products for cancer prevention and therapy

非西汀 药理学 癌症 癌症预防 医学 姜黄素 白藜芦醇 穿心莲内酯 化学 生物化学 抗氧化剂 内科学 类黄酮
作者
Nagendra Sastry Yarla,Anupam Bishayee,Gautam Sethi,Pallu Reddanna,Arunasree M. Kalle,Bhadrapura Lakkappa Dhananjaya,D. S. V. G. K. Kaladhar,Ramakrishna Chintala,Govinda Rao Duddukuri
出处
期刊:Seminars in Cancer Biology [Elsevier BV]
卷期号:40-41: 48-81 被引量:365
标识
DOI:10.1016/j.semcancer.2016.02.001
摘要

Arachidonic acid (AA) pathway, a metabolic process, plays a key role in carcinogenesis. Hence, AA pathway metabolic enzymes phospholipase A2s (PLA2s), cyclooxygenases (COXs) and lipoxygenases (LOXs) and their metabolic products, such as prostaglandins and leukotrienes, have been considered novel preventive and therapeutic targets in cancer. Bioactive natural products are a good source for development of novel cancer preventive and therapeutic drugs, which have been widely used in clinical practice due to their safety profiles. AA pathway inhibitory natural products have been developed as chemopreventive and therapeutic agents against several cancers. Curcumin, resveratrol, apigenin, anthocyans, berberine, ellagic acid, eugenol, fisetin, ursolic acid, [6]-gingerol, guggulsteone, lycopene and genistein are well known cancer chemopreventive agents which act by targeting multiple pathways, including COX-2. Nordihydroguaiaretic acid and baicalein can be chemopreventive molecules against various cancers by inhibiting LOXs. Several PLA2s inhibitory natural products have been identified with chemopreventive and therapeutic potentials against various cancers. In this review, we critically discuss the possible utility of natural products as preventive and therapeutic agents against various oncologic diseases, including prostate, pancreatic, lung, skin, gastric, oral, blood, head and neck, colorectal, liver, cervical and breast cancers, by targeting AA pathway. Further, the current status of clinical studies evaluating AA pathway inhibitory natural products in cancer is reviewed. In addition, various emerging issues, including bioavailability, toxicity and explorability of combination therapy, for the development of AA pathway inhibitory natural products as chemopreventive and therapeutic agents against human malignancy are also discussed.
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