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Effect of red clover isoflavones on cox-2 activity in murine and human monocyte/macrophage cells

Long-term use of nonsteroidal anti-inflammatory drugs is associated with a reduction in the incidence of a range of cancers, the mechanism of which is thought to be cyclooxygenase (COX) inhibition. Because long-term ingestion of foods rich in isoflavones, such as legumes (beans, peas, lentils) has b...

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Published in:Nutrition and cancer 2004-01, Vol.49 (1), p.89-93
Main Authors: Lam, A.N.C, Demasi, M, James, M.J, Husband, A.J, Walker, C
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container_title Nutrition and cancer
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creator Lam, A.N.C
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description Long-term use of nonsteroidal anti-inflammatory drugs is associated with a reduction in the incidence of a range of cancers, the mechanism of which is thought to be cyclooxygenase (COX) inhibition. Because long-term ingestion of foods rich in isoflavones, such as legumes (beans, peas, lentils) has been associated with reduced cancer incidence, it was considered useful to examine the COX-inhibitory activities of individual isoflavones. Red clover dietary supplements also contain varying ratios of the 4 isoflavones commonly found in legume-based diets, namely, daidzein, genistein, formononetin, and biochanin. Using 2 separate cell assays, this study examined the ability of the isoflavones found in red clover to inhibit COX enzyme activity in both the murine macrophage cell line RAW 264.7 and human monocytes. Within the range of 1-40 micromolar in RAW 264.7 cells and 10-100 micromolar in human monocytes, isoflavones were able to reduce significantly the synthesis of prostaglandin E2 and/or thromboxane B2 (P < 0.001 to P < 0.05), indicating COX inhibition. Thus, it is possible that the lower rates of some cancers in populations with a high intake of dietary isoflavones is linked to their inhibition of COX activity.
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Thus, it is possible that the lower rates of some cancers in populations with a high intake of dietary isoflavones is linked to their inhibition of COX activity.</description><subject>Animals</subject><subject>Anticarcinogenic Agents - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Cells, Cultured</subject><subject>Cyclooxygenase 2</subject><subject>Dietary Supplements</subject><subject>Dinoprostone - biosynthesis</subject><subject>Dose-Response Relationship, Drug</subject><subject>enzyme activity</subject><subject>Feeding. Feeding behavior</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genistein - pharmacology</subject><subject>human health</subject><subject>human nutrition</subject><subject>Humans</subject><subject>isoflavones</subject><subject>Isoflavones - pharmacology</subject><subject>macrophages</subject><subject>Macrophages - enzymology</subject><subject>Medical sciences</subject><subject>Membrane Proteins</subject><subject>Metabolic diseases</subject><subject>Mice</subject><subject>monocytes</subject><subject>Monocytes - enzymology</subject><subject>phytochemicals</subject><subject>prostaglandin synthase</subject><subject>Prostaglandin-Endoperoxide Synthases - drug effects</subject><subject>Prostaglandin-Endoperoxide Synthases - metabolism</subject><subject>Thromboxane B2 - biosynthesis</subject><subject>Trifolium - chemistry</subject><subject>Trifolium pratense</subject><subject>Tumors</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><issn>0163-5581</issn><issn>1532-7914</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNp9kEtv1DAUhS1ERYfCH2AB3sAurd-JFyyqqjykSiyga3PjR2uU2IOdDMy_b6IZ1AVSN7Z09H1XRwehN5ScU0bai0olZ62mIlmhCTWUPUObNWvW8DnaEKp4I2VHT9HLWn8RQlrKuxfolEohlRJkg35eh-DthHPAxTtsh7zzBceawwC7nHzFOWGb_zYMg53iLk57HBMe5xKTx5Acvp9HWIKcst1P_mIEW_L2Hu48tn4Y6it0EmCo_vXxP0O3n65_XH1pbr59_np1edNYQdqpoR0DEMq1jnSKeUG4VKx1QYDmVC-vDYRz0SntHBHQ9dz1lATmFs32veZn6MPh7rbk37OvkxljXRtA8nmuRinNhOZ8AdkBXHrWWnww2xJHKHtDiVl3Nf_vukhvj9fnfvTuUTkOuQDvjwBUC0MokGysj5yiTFO51vx44GIKuYzwJ5fBmQn2Qy7_JP5kkXcHP0A2cFcW_PY7I5QToqVkUvIHplWeTg</recordid><startdate>20040101</startdate><enddate>20040101</enddate><creator>Lam, A.N.C</creator><creator>Demasi, M</creator><creator>James, M.J</creator><creator>Husband, A.J</creator><creator>Walker, C</creator><general>Lawrence Erlbaum Associates, Inc</general><general>Taylor&amp; Francis</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20040101</creationdate><title>Effect of red clover isoflavones on cox-2 activity in murine and human monocyte/macrophage cells</title><author>Lam, A.N.C ; Demasi, M ; James, M.J ; Husband, A.J ; Walker, C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c407t-182aa46d7d0862e4035627df4a93194a9cf0334869dd04a8b3db10f2d2aacbb93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Anticarcinogenic Agents - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Cells, Cultured</topic><topic>Cyclooxygenase 2</topic><topic>Dietary Supplements</topic><topic>Dinoprostone - biosynthesis</topic><topic>Dose-Response Relationship, Drug</topic><topic>enzyme activity</topic><topic>Feeding. Feeding behavior</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genistein - pharmacology</topic><topic>human health</topic><topic>human nutrition</topic><topic>Humans</topic><topic>isoflavones</topic><topic>Isoflavones - pharmacology</topic><topic>macrophages</topic><topic>Macrophages - enzymology</topic><topic>Medical sciences</topic><topic>Membrane Proteins</topic><topic>Metabolic diseases</topic><topic>Mice</topic><topic>monocytes</topic><topic>Monocytes - enzymology</topic><topic>phytochemicals</topic><topic>prostaglandin synthase</topic><topic>Prostaglandin-Endoperoxide Synthases - drug effects</topic><topic>Prostaglandin-Endoperoxide Synthases - metabolism</topic><topic>Thromboxane B2 - biosynthesis</topic><topic>Trifolium - chemistry</topic><topic>Trifolium pratense</topic><topic>Tumors</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lam, A.N.C</creatorcontrib><creatorcontrib>Demasi, M</creatorcontrib><creatorcontrib>James, M.J</creatorcontrib><creatorcontrib>Husband, A.J</creatorcontrib><creatorcontrib>Walker, C</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Nutrition and cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lam, A.N.C</au><au>Demasi, M</au><au>James, M.J</au><au>Husband, A.J</au><au>Walker, C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of red clover isoflavones on cox-2 activity in murine and human monocyte/macrophage cells</atitle><jtitle>Nutrition and cancer</jtitle><addtitle>Nutr Cancer</addtitle><date>2004-01-01</date><risdate>2004</risdate><volume>49</volume><issue>1</issue><spage>89</spage><epage>93</epage><pages>89-93</pages><issn>0163-5581</issn><eissn>1532-7914</eissn><coden>NUCADQ</coden><abstract>Long-term use of nonsteroidal anti-inflammatory drugs is associated with a reduction in the incidence of a range of cancers, the mechanism of which is thought to be cyclooxygenase (COX) inhibition. Because long-term ingestion of foods rich in isoflavones, such as legumes (beans, peas, lentils) has been associated with reduced cancer incidence, it was considered useful to examine the COX-inhibitory activities of individual isoflavones. Red clover dietary supplements also contain varying ratios of the 4 isoflavones commonly found in legume-based diets, namely, daidzein, genistein, formononetin, and biochanin. Using 2 separate cell assays, this study examined the ability of the isoflavones found in red clover to inhibit COX enzyme activity in both the murine macrophage cell line RAW 264.7 and human monocytes. Within the range of 1-40 micromolar in RAW 264.7 cells and 10-100 micromolar in human monocytes, isoflavones were able to reduce significantly the synthesis of prostaglandin E2 and/or thromboxane B2 (P &lt; 0.001 to P &lt; 0.05), indicating COX inhibition. 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source Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Medical Collection (Reading list)
subjects Animals
Anticarcinogenic Agents - pharmacology
Biological and medical sciences
Cells, Cultured
Cyclooxygenase 2
Dietary Supplements
Dinoprostone - biosynthesis
Dose-Response Relationship, Drug
enzyme activity
Feeding. Feeding behavior
Fundamental and applied biological sciences. Psychology
Genistein - pharmacology
human health
human nutrition
Humans
isoflavones
Isoflavones - pharmacology
macrophages
Macrophages - enzymology
Medical sciences
Membrane Proteins
Metabolic diseases
Mice
monocytes
Monocytes - enzymology
phytochemicals
prostaglandin synthase
Prostaglandin-Endoperoxide Synthases - drug effects
Prostaglandin-Endoperoxide Synthases - metabolism
Thromboxane B2 - biosynthesis
Trifolium - chemistry
Trifolium pratense
Tumors
Vertebrates: anatomy and physiology, studies on body, several organs or systems
title Effect of red clover isoflavones on cox-2 activity in murine and human monocyte/macrophage cells
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