Effects of an eicosapentaenoic and docosahexaenoic acid concentrate on a human lung carcinoma grown in nude mice
The effects of the n−3 fatty acids, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), on the growth of a human lung mucoepidermoid carcinoma (HLMC) in athymic mice were studied. The mice were divided into three groups which were given either a control chow diet (C), a chow diet supplemente...
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Veröffentlicht in: | Lipids 1991-11, Vol.26 (11), p.866-870 |
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description | The effects of the n−3 fatty acids, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), on the growth of a human lung mucoepidermoid carcinoma (HLMC) in athymic mice were studied. The mice were divided into three groups which were given either a control chow diet (C), a chow diet supplemented with EPA/DHA (P) (25 or 50 mg of free n−3 fatty acids/g of pellet/day), or chow diet supplemented with palmitic acid (S) (isocaloric with P). Two independent experimental schedules were followed: i) host mice bearing either tumors that were allowed to reach 4000 mm3, or only 35 mm3, were fed C, P or S for 21 or 41 days; ii) animals were fed C, P and S for 9 days before tumor implant and were maintained on these diets throughout tumor growth. Food consumption, mouse weight and liver/body weight ratio showed no significant differences between supplemented diets and chow. Tumor growth was markedly inhibited (45%) in both experiments by the EPA/DHA supplemented diet. In Experiment 2, only 60% of mice fed diet P had tumors. The fatty acid composition of neutral and polar lipids of host liver and tumor reflected the dietary intake of n−3 fatty acids; the content of arachidonic acid was reduced by 50%, and EPA/DHA was increased 3‐to 5‐fold. Tumor prostaglandin E2 levels were reduced 7.4‐fold in the P group. The reduced PGE2 content may be a factor in tumor growth inhibition. |
doi_str_mv | 10.1007/BF02535969 |
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G. ; Antueno, R. J. ; Toledo, J. ; De Tomás, M. E. ; Mercuri, O. F. ; Quintans, C.</creator><creatorcontrib>Bravo, M. G. ; Antueno, R. J. ; Toledo, J. ; De Tomás, M. E. ; Mercuri, O. F. ; Quintans, C.</creatorcontrib><description>The effects of the n−3 fatty acids, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), on the growth of a human lung mucoepidermoid carcinoma (HLMC) in athymic mice were studied. The mice were divided into three groups which were given either a control chow diet (C), a chow diet supplemented with EPA/DHA (P) (25 or 50 mg of free n−3 fatty acids/g of pellet/day), or chow diet supplemented with palmitic acid (S) (isocaloric with P). Two independent experimental schedules were followed: i) host mice bearing either tumors that were allowed to reach 4000 mm3, or only 35 mm3, were fed C, P or S for 21 or 41 days; ii) animals were fed C, P and S for 9 days before tumor implant and were maintained on these diets throughout tumor growth. Food consumption, mouse weight and liver/body weight ratio showed no significant differences between supplemented diets and chow. Tumor growth was markedly inhibited (45%) in both experiments by the EPA/DHA supplemented diet. In Experiment 2, only 60% of mice fed diet P had tumors. The fatty acid composition of neutral and polar lipids of host liver and tumor reflected the dietary intake of n−3 fatty acids; the content of arachidonic acid was reduced by 50%, and EPA/DHA was increased 3‐to 5‐fold. Tumor prostaglandin E2 levels were reduced 7.4‐fold in the P group. The reduced PGE2 content may be a factor in tumor growth inhibition.</description><identifier>ISSN: 0024-4201</identifier><identifier>EISSN: 1558-9307</identifier><identifier>DOI: 10.1007/BF02535969</identifier><identifier>PMID: 1839563</identifier><identifier>CODEN: LPDSAP</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer‐Verlag</publisher><subject>Analytical, structural and metabolic biochemistry ; Animals ; Arachidonic Acid - metabolism ; Biological and medical sciences ; Carcinoma - etiology ; Dietary Fats - pharmacology ; Dinoprostone - metabolism ; Docosahexaenoic Acids - pharmacology ; Eicosapentaenoic Acid - pharmacology ; Fatty Acids - metabolism ; Fatty Acids, Omega-3 - pharmacology ; Fish Oils - pharmacology ; Fundamental and applied biological sciences. 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G.</creatorcontrib><creatorcontrib>Antueno, R. J.</creatorcontrib><creatorcontrib>Toledo, J.</creatorcontrib><creatorcontrib>De Tomás, M. E.</creatorcontrib><creatorcontrib>Mercuri, O. F.</creatorcontrib><creatorcontrib>Quintans, C.</creatorcontrib><title>Effects of an eicosapentaenoic and docosahexaenoic acid concentrate on a human lung carcinoma grown in nude mice</title><title>Lipids</title><addtitle>Lipids</addtitle><description>The effects of the n−3 fatty acids, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), on the growth of a human lung mucoepidermoid carcinoma (HLMC) in athymic mice were studied. The mice were divided into three groups which were given either a control chow diet (C), a chow diet supplemented with EPA/DHA (P) (25 or 50 mg of free n−3 fatty acids/g of pellet/day), or chow diet supplemented with palmitic acid (S) (isocaloric with P). Two independent experimental schedules were followed: i) host mice bearing either tumors that were allowed to reach 4000 mm3, or only 35 mm3, were fed C, P or S for 21 or 41 days; ii) animals were fed C, P and S for 9 days before tumor implant and were maintained on these diets throughout tumor growth. Food consumption, mouse weight and liver/body weight ratio showed no significant differences between supplemented diets and chow. Tumor growth was markedly inhibited (45%) in both experiments by the EPA/DHA supplemented diet. In Experiment 2, only 60% of mice fed diet P had tumors. The fatty acid composition of neutral and polar lipids of host liver and tumor reflected the dietary intake of n−3 fatty acids; the content of arachidonic acid was reduced by 50%, and EPA/DHA was increased 3‐to 5‐fold. Tumor prostaglandin E2 levels were reduced 7.4‐fold in the P group. The reduced PGE2 content may be a factor in tumor growth inhibition.</description><subject>Analytical, structural and metabolic biochemistry</subject><subject>Animals</subject><subject>Arachidonic Acid - metabolism</subject><subject>Biological and medical sciences</subject><subject>Carcinoma - etiology</subject><subject>Dietary Fats - pharmacology</subject><subject>Dinoprostone - metabolism</subject><subject>Docosahexaenoic Acids - pharmacology</subject><subject>Eicosapentaenoic Acid - pharmacology</subject><subject>Fatty Acids - metabolism</subject><subject>Fatty Acids, Omega-3 - pharmacology</subject><subject>Fish Oils - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Liver - chemistry</subject><subject>Lung Neoplasms - etiology</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Nude</subject><subject>Other biological molecules</subject><issn>0024-4201</issn><issn>1558-9307</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEFv1DAQhS0EapfChXslHxAHpMA4ju34SMsWKq0EBzhHzmTcukrsxd6o7b8nq93SG6fRe-_TG-kx9k7AJwFgPl9cQa2kstq-YCuhVFtZCeYlWwHUTdXUIE7Z61LuFikaq07YiWilVVqu2HbtPeGu8OS5i5wCpuK2FHeOYgq4eAMf0t68pYcnD8PAMUVcsOx2xFPkjt_O01IwzvGGo8sYYpocv8npPvIQeZwH4lNAesNeeTcWenu8Z-z31frX5fdq8-Pb9eWXTYWNaHVlFNU9OC974Qc0slGget9bsNJiY3toyS-y1kobFDWZ3teqF2oQg_JaG3nGPhx6tzn9mansuikUpHF0kdJcOlMbECBhAT8eQMyplEy-2-YwufzYCej283bP8y7w-bF17icantHDnkv-_pi7gm702UUM5R_WSNFau6-BA3YfRnr8z8Nuc_3zK7Ray78HzZCB</recordid><startdate>199111</startdate><enddate>199111</enddate><creator>Bravo, M. G.</creator><creator>Antueno, R. J.</creator><creator>Toledo, J.</creator><creator>De Tomás, M. E.</creator><creator>Mercuri, O. F.</creator><creator>Quintans, C.</creator><general>Springer‐Verlag</general><general>Springer</general><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>199111</creationdate><title>Effects of an eicosapentaenoic and docosahexaenoic acid concentrate on a human lung carcinoma grown in nude mice</title><author>Bravo, M. G. ; Antueno, R. J. ; Toledo, J. ; De Tomás, M. E. ; Mercuri, O. F. ; Quintans, C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4186-75e2b0af3b1fdc734505bfb90939c49b08effb926567c12e7bf25b15d1d5f6673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Analytical, structural and metabolic biochemistry</topic><topic>Animals</topic><topic>Arachidonic Acid - metabolism</topic><topic>Biological and medical sciences</topic><topic>Carcinoma - etiology</topic><topic>Dietary Fats - pharmacology</topic><topic>Dinoprostone - metabolism</topic><topic>Docosahexaenoic Acids - pharmacology</topic><topic>Eicosapentaenoic Acid - pharmacology</topic><topic>Fatty Acids - metabolism</topic><topic>Fatty Acids, Omega-3 - pharmacology</topic><topic>Fish Oils - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Liver - chemistry</topic><topic>Lung Neoplasms - etiology</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Nude</topic><topic>Other biological molecules</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bravo, M. G.</creatorcontrib><creatorcontrib>Antueno, R. J.</creatorcontrib><creatorcontrib>Toledo, J.</creatorcontrib><creatorcontrib>De Tomás, M. E.</creatorcontrib><creatorcontrib>Mercuri, O. F.</creatorcontrib><creatorcontrib>Quintans, C.</creatorcontrib><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>Lipids</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bravo, M. G.</au><au>Antueno, R. J.</au><au>Toledo, J.</au><au>De Tomás, M. E.</au><au>Mercuri, O. F.</au><au>Quintans, C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of an eicosapentaenoic and docosahexaenoic acid concentrate on a human lung carcinoma grown in nude mice</atitle><jtitle>Lipids</jtitle><addtitle>Lipids</addtitle><date>1991-11</date><risdate>1991</risdate><volume>26</volume><issue>11</issue><spage>866</spage><epage>870</epage><pages>866-870</pages><issn>0024-4201</issn><eissn>1558-9307</eissn><coden>LPDSAP</coden><abstract>The effects of the n−3 fatty acids, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), on the growth of a human lung mucoepidermoid carcinoma (HLMC) in athymic mice were studied. The mice were divided into three groups which were given either a control chow diet (C), a chow diet supplemented with EPA/DHA (P) (25 or 50 mg of free n−3 fatty acids/g of pellet/day), or chow diet supplemented with palmitic acid (S) (isocaloric with P). Two independent experimental schedules were followed: i) host mice bearing either tumors that were allowed to reach 4000 mm3, or only 35 mm3, were fed C, P or S for 21 or 41 days; ii) animals were fed C, P and S for 9 days before tumor implant and were maintained on these diets throughout tumor growth. Food consumption, mouse weight and liver/body weight ratio showed no significant differences between supplemented diets and chow. Tumor growth was markedly inhibited (45%) in both experiments by the EPA/DHA supplemented diet. In Experiment 2, only 60% of mice fed diet P had tumors. The fatty acid composition of neutral and polar lipids of host liver and tumor reflected the dietary intake of n−3 fatty acids; the content of arachidonic acid was reduced by 50%, and EPA/DHA was increased 3‐to 5‐fold. Tumor prostaglandin E2 levels were reduced 7.4‐fold in the P group. The reduced PGE2 content may be a factor in tumor growth inhibition.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer‐Verlag</pub><pmid>1839563</pmid><doi>10.1007/BF02535969</doi><tpages>5</tpages></addata></record> |
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subjects | Analytical, structural and metabolic biochemistry Animals Arachidonic Acid - metabolism Biological and medical sciences Carcinoma - etiology Dietary Fats - pharmacology Dinoprostone - metabolism Docosahexaenoic Acids - pharmacology Eicosapentaenoic Acid - pharmacology Fatty Acids - metabolism Fatty Acids, Omega-3 - pharmacology Fish Oils - pharmacology Fundamental and applied biological sciences. Psychology Liver - chemistry Lung Neoplasms - etiology Mice Mice, Inbred BALB C Mice, Nude Other biological molecules |
title | Effects of an eicosapentaenoic and docosahexaenoic acid concentrate on a human lung carcinoma grown in nude mice |
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