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Comparative study of the effects of polyunsaturated fatty acids and their metabolites on cell growth and tyrosine kinase activity in oesophageal carcinoma cells
The effects of exogenous γ-linolenic acid (GLA), arachidonic acid (AA), prostaglandin E2(PGE2) and prostaglandin A2(PGA2) were evaluated on cell growth in two squamous oesophageal carcinoma cell lines, WHCO1 and WHCO3 and normal monkey kidney (NMK) cells. In both cancer cell lines all four compounds...
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Published in: | Prostaglandins, leukotrienes and essential fatty acids leukotrienes and essential fatty acids, 1999-09, Vol.61 (3), p.171-182 |
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creator | Joubert, A.M. Panzer, A. Joubert, F. Lottering, M.-L. Bianchi, P.C. Seegers, J.C. |
description | The effects of exogenous γ-linolenic acid (GLA), arachidonic acid (AA), prostaglandin E2(PGE2) and prostaglandin A2(PGA2) were evaluated on cell growth in two squamous oesophageal carcinoma cell lines, WHCO1 and WHCO3 and normal monkey kidney (NMK) cells. In both cancer cell lines all four compounds inhibited cell growth significantly. Indomethacin (I) alone, or in combination with either GLA or AA, caused marked inhibition of cell growth in WHCO3. Total tyrosine kinase (TK) activity was determined after exposure of all three cell types to the lipid compounds. Negligible differences were observed in TK activity between treated and untreated NMK cells. Small increases were noticed in WHCO1. Marked TK stimulation was observed in WHCO3. Addition of indomethacin to WHCO3 also increased TK activity above control value. Tyrosine phosphorylation status of exposed cells indicated that a band of approximately 55kDa (55kDa) was primarily influenced in both WHCO3 and WHCO1. PGA2caused a decrease in tyrosine phosphorylation of the 55kDa protein in all three cell types. Negligible differences were observed in the tyrosine phosphorylation status of the 55kDa in NMK cells exposed to GLA, AA and PGE2respectively. However, tyrosine phosphorylation of a number of other proteins (21.5-97.4kDa) was observed in NMK cells. Flow cytometry studies showed an increase in S phase and decrease in G1 phase in WHCO3 exposed to PGE2and PGA2. Indomethacin alone, or in combination with GLA and AA, respectively, lead to an increase in G1and a decrease in S phase. Induction of p53 levels was observed in WHCO3 cells exposed to GLA, AA, PGA2, indomethacin and the combination of indomethacin and GLA or AA. |
doi_str_mv | 10.1054/plef.1999.0087 |
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In both cancer cell lines all four compounds inhibited cell growth significantly. Indomethacin (I) alone, or in combination with either GLA or AA, caused marked inhibition of cell growth in WHCO3. Total tyrosine kinase (TK) activity was determined after exposure of all three cell types to the lipid compounds. Negligible differences were observed in TK activity between treated and untreated NMK cells. Small increases were noticed in WHCO1. Marked TK stimulation was observed in WHCO3. Addition of indomethacin to WHCO3 also increased TK activity above control value. Tyrosine phosphorylation status of exposed cells indicated that a band of approximately 55kDa (55kDa) was primarily influenced in both WHCO3 and WHCO1. PGA2caused a decrease in tyrosine phosphorylation of the 55kDa protein in all three cell types. Negligible differences were observed in the tyrosine phosphorylation status of the 55kDa in NMK cells exposed to GLA, AA and PGE2respectively. However, tyrosine phosphorylation of a number of other proteins (21.5-97.4kDa) was observed in NMK cells. Flow cytometry studies showed an increase in S phase and decrease in G1 phase in WHCO3 exposed to PGE2and PGA2. Indomethacin alone, or in combination with GLA and AA, respectively, lead to an increase in G1and a decrease in S phase. 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In both cancer cell lines all four compounds inhibited cell growth significantly. Indomethacin (I) alone, or in combination with either GLA or AA, caused marked inhibition of cell growth in WHCO3. Total tyrosine kinase (TK) activity was determined after exposure of all three cell types to the lipid compounds. Negligible differences were observed in TK activity between treated and untreated NMK cells. Small increases were noticed in WHCO1. Marked TK stimulation was observed in WHCO3. Addition of indomethacin to WHCO3 also increased TK activity above control value. Tyrosine phosphorylation status of exposed cells indicated that a band of approximately 55kDa (55kDa) was primarily influenced in both WHCO3 and WHCO1. PGA2caused a decrease in tyrosine phosphorylation of the 55kDa protein in all three cell types. Negligible differences were observed in the tyrosine phosphorylation status of the 55kDa in NMK cells exposed to GLA, AA and PGE2respectively. However, tyrosine phosphorylation of a number of other proteins (21.5-97.4kDa) was observed in NMK cells. Flow cytometry studies showed an increase in S phase and decrease in G1 phase in WHCO3 exposed to PGE2and PGA2. Indomethacin alone, or in combination with GLA and AA, respectively, lead to an increase in G1and a decrease in S phase. Induction of p53 levels was observed in WHCO3 cells exposed to GLA, AA, PGA2, indomethacin and the combination of indomethacin and GLA or AA.</description><subject>Animals</subject><subject>Arachidonic Acid - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Squamous Cell - enzymology</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Cell Division - drug effects</subject><subject>Cell Line</subject><subject>Cercopithecus aethiops</subject><subject>Dinoprostone - pharmacology</subject><subject>Esophageal Neoplasms - enzymology</subject><subject>Esophageal Neoplasms - pathology</subject><subject>Fatty Acids, Unsaturated - pharmacology</subject><subject>Flow Cytometry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>gamma-Linolenic Acid - pharmacology</subject><subject>Humans</subject><subject>Kidney</subject><subject>Mouth. Exocrine and endocrine salivary glands. Teeth. Esophagus</subject><subject>Phosphorylation</subject><subject>Prostaglandins A - pharmacology</subject><subject>Protein-Tyrosine Kinases - metabolism</subject><subject>Tumor Cells, Cultured</subject><subject>Tumor Suppressor Protein p53 - analysis</subject><subject>Tyrosine - metabolism</subject><subject>Vertebrates: digestive system</subject><issn>0952-3278</issn><issn>1532-2823</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNp1kU2P1SAUhonROHdGty4NC-OuV6ClH0tzMzomk7jRNTmF07loCxXomP4bf6rU3kQ3rgjJ874czkPIK86OnMnq3TzicORd1x0Za5sn5MBlKQrRivIpObBOiqIUTXtFrmP8xhgTnFfPyVWOtqKWzYH8OvlphgDJPiKNaTEr9QNNZ6Q4DKhT3K6zH9fFRUhLBtHQAVJaKWhrIgVnNtwGOmGC3o82YQ45qnEc6UPwP9N5h9bgo3VIv1sHEXM8v2lzj3XUY_TzGR4QRqohaOv8BH8a4gvybIAx4svLeUO-frj9cror7j9__HR6f1_osu5S0YtKa4Bac90z2bWaG9liBT2XvWRYs1qaRiMOUmNTCamFMNuqWs6MLquhvCFv9945-B8LxqQmG7cJwKFfoqq7spQ1bzN43EGd_xMDDmoOdoKwKs7U5kRtTtTmRG1OcuD1pXnpJzT_4LuEDLy5ABA1jEMAp238ywlZlbzOWLtjmNfwaDGoqC06jcaGbEoZb_83wm8H3qyx</recordid><startdate>19990901</startdate><enddate>19990901</enddate><creator>Joubert, A.M.</creator><creator>Panzer, A.</creator><creator>Joubert, F.</creator><creator>Lottering, M.-L.</creator><creator>Bianchi, P.C.</creator><creator>Seegers, J.C.</creator><general>Elsevier Ltd</general><general>Elsevier</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>19990901</creationdate><title>Comparative study of the effects of polyunsaturated fatty acids and their metabolites on cell growth and tyrosine kinase activity in oesophageal carcinoma cells</title><author>Joubert, A.M. ; Panzer, A. ; Joubert, F. ; Lottering, M.-L. ; Bianchi, P.C. ; Seegers, J.C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c369t-b24ccaa6c1cb0598c1d58e4ab15b50e6065d7ceef5ce7425c22d1532810dc34f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>Arachidonic Acid - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Carcinoma, Squamous Cell - enzymology</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Cell Division - drug effects</topic><topic>Cell Line</topic><topic>Cercopithecus aethiops</topic><topic>Dinoprostone - pharmacology</topic><topic>Esophageal Neoplasms - enzymology</topic><topic>Esophageal Neoplasms - pathology</topic><topic>Fatty Acids, Unsaturated - pharmacology</topic><topic>Flow Cytometry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>gamma-Linolenic Acid - pharmacology</topic><topic>Humans</topic><topic>Kidney</topic><topic>Mouth. Exocrine and endocrine salivary glands. Teeth. Esophagus</topic><topic>Phosphorylation</topic><topic>Prostaglandins A - pharmacology</topic><topic>Protein-Tyrosine Kinases - metabolism</topic><topic>Tumor Cells, Cultured</topic><topic>Tumor Suppressor Protein p53 - analysis</topic><topic>Tyrosine - metabolism</topic><topic>Vertebrates: digestive system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Joubert, A.M.</creatorcontrib><creatorcontrib>Panzer, A.</creatorcontrib><creatorcontrib>Joubert, F.</creatorcontrib><creatorcontrib>Lottering, M.-L.</creatorcontrib><creatorcontrib>Bianchi, P.C.</creatorcontrib><creatorcontrib>Seegers, J.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>Prostaglandins, leukotrienes and essential fatty acids</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Joubert, A.M.</au><au>Panzer, A.</au><au>Joubert, F.</au><au>Lottering, M.-L.</au><au>Bianchi, P.C.</au><au>Seegers, J.C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative study of the effects of polyunsaturated fatty acids and their metabolites on cell growth and tyrosine kinase activity in oesophageal carcinoma cells</atitle><jtitle>Prostaglandins, leukotrienes and essential fatty acids</jtitle><addtitle>Prostaglandins Leukot Essent Fatty Acids</addtitle><date>1999-09-01</date><risdate>1999</risdate><volume>61</volume><issue>3</issue><spage>171</spage><epage>182</epage><pages>171-182</pages><issn>0952-3278</issn><eissn>1532-2823</eissn><abstract>The effects of exogenous γ-linolenic acid (GLA), arachidonic acid (AA), prostaglandin E2(PGE2) and prostaglandin A2(PGA2) were evaluated on cell growth in two squamous oesophageal carcinoma cell lines, WHCO1 and WHCO3 and normal monkey kidney (NMK) cells. In both cancer cell lines all four compounds inhibited cell growth significantly. Indomethacin (I) alone, or in combination with either GLA or AA, caused marked inhibition of cell growth in WHCO3. Total tyrosine kinase (TK) activity was determined after exposure of all three cell types to the lipid compounds. Negligible differences were observed in TK activity between treated and untreated NMK cells. Small increases were noticed in WHCO1. Marked TK stimulation was observed in WHCO3. Addition of indomethacin to WHCO3 also increased TK activity above control value. Tyrosine phosphorylation status of exposed cells indicated that a band of approximately 55kDa (55kDa) was primarily influenced in both WHCO3 and WHCO1. PGA2caused a decrease in tyrosine phosphorylation of the 55kDa protein in all three cell types. Negligible differences were observed in the tyrosine phosphorylation status of the 55kDa in NMK cells exposed to GLA, AA and PGE2respectively. However, tyrosine phosphorylation of a number of other proteins (21.5-97.4kDa) was observed in NMK cells. Flow cytometry studies showed an increase in S phase and decrease in G1 phase in WHCO3 exposed to PGE2and PGA2. Indomethacin alone, or in combination with GLA and AA, respectively, lead to an increase in G1and a decrease in S phase. Induction of p53 levels was observed in WHCO3 cells exposed to GLA, AA, PGA2, indomethacin and the combination of indomethacin and GLA or AA.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>10582657</pmid><doi>10.1054/plef.1999.0087</doi><tpages>12</tpages></addata></record> |
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subjects | Animals Arachidonic Acid - pharmacology Biological and medical sciences Carcinoma, Squamous Cell - enzymology Carcinoma, Squamous Cell - pathology Cell Division - drug effects Cell Line Cercopithecus aethiops Dinoprostone - pharmacology Esophageal Neoplasms - enzymology Esophageal Neoplasms - pathology Fatty Acids, Unsaturated - pharmacology Flow Cytometry Fundamental and applied biological sciences. Psychology gamma-Linolenic Acid - pharmacology Humans Kidney Mouth. Exocrine and endocrine salivary glands. Teeth. Esophagus Phosphorylation Prostaglandins A - pharmacology Protein-Tyrosine Kinases - metabolism Tumor Cells, Cultured Tumor Suppressor Protein p53 - analysis Tyrosine - metabolism Vertebrates: digestive system |
title | Comparative study of the effects of polyunsaturated fatty acids and their metabolites on cell growth and tyrosine kinase activity in oesophageal carcinoma cells |
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