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非甾体抗炎药、前列腺素与癌症。

Non-steroid anti-inflammatory drugs, prostaglandins, and cancer.

机构信息

Department of Medical Microbiology, Immunology, and Cell Biology, Southern Illinois University School of Medicine and Simmons Cancer Institute, Springfield, IL, 62794, USA.

出版信息

Cell Biosci. 2013 Feb 6;3(1):8. doi: 10.1186/2045-3701-3-8.

Abstract

Fatty acids are involved in multiple pathways and play a pivotal role in health. Eicosanoids, derived from arachidonic acid, have received extensive attention in the field of cancer research. Following release from the phospholipid membrane, arachidonic acid can be metabolized into different classes of eicosanoids through cyclooxygenases, lipoxygenases, or p450 epoxygenase pathways. Non-steroid anti-inflammatory drugs (NSAIDs) are widely consumed as analgesics to relieve minor aches and pains, as antipyretics to reduce fever, and as anti-inflammatory medications. Most NSAIDs are nonselective inhibitors of cyclooxygenases, the rate limiting enzymes in the formation of prostaglandins. Long term use of some NSAIDs has been linked with reduced incidence and mortality in many cancers. In this review, we appraise the biological activities of prostanoids and their cognate receptors in the context of cancer biology. The existing literature supports that these lipid mediators are involved to a great extent in the occurrence and progression of cancer.

摘要

脂肪酸参与多种途径,在健康中发挥关键作用。类二十烷酸源于花生四烯酸,在癌症研究领域受到广泛关注。花生四烯酸从磷脂膜释放后,可以通过环加氧酶、脂加氧酶或 p450 环氧合酶途径代谢成不同类别的类二十烷酸。非甾体抗炎药(NSAIDs)作为镇痛药广泛用于缓解轻微疼痛,作为退烧药用于降低体温,作为抗炎药使用。大多数 NSAIDs 是非选择性环加氧酶抑制剂,环加氧酶是前列腺素形成的限速酶。长期使用某些 NSAIDs 与许多癌症的发病率和死亡率降低有关。在这篇综述中,我们评估了前列腺素及其同源受体在癌症生物学中的生物学活性。现有文献表明,这些脂类介质在癌症的发生和发展中起了很大的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d35a/3599181/dbff875b6374/2045-3701-3-8-1.jpg

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