Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Prostaglandins, leukotrienes and essential fatty acids leukotrienes and essential fatty acids, 1999-09, Vol.61 (3), p.171-182
Main Authors: Joubert, A.M., Panzer, A., Joubert, F., Lottering, M.-L., Bianchi, P.C., Seegers, J.C.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c369t-b24ccaa6c1cb0598c1d58e4ab15b50e6065d7ceef5ce7425c22d1532810dc34f3
cites cdi_FETCH-LOGICAL-c369t-b24ccaa6c1cb0598c1d58e4ab15b50e6065d7ceef5ce7425c22d1532810dc34f3
container_end_page 182
container_issue 3
container_start_page 171
container_title Prostaglandins, leukotrienes and essential fatty acids
container_volume 61
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
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_69335618</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S095232789990087X</els_id><sourcerecordid>69335618</sourcerecordid><originalsourceid>FETCH-LOGICAL-c369t-b24ccaa6c1cb0598c1d58e4ab15b50e6065d7ceef5ce7425c22d1532810dc34f3</originalsourceid><addsrcrecordid>eNp1kU2P1SAUhonROHdGty4NC-OuV6ClH0tzMzomk7jRNTmF07loCxXomP4bf6rU3kQ3rgjJ874czkPIK86OnMnq3TzicORd1x0Za5sn5MBlKQrRivIpObBOiqIUTXtFrmP8xhgTnFfPyVWOtqKWzYH8OvlphgDJPiKNaTEr9QNNZ6Q4DKhT3K6zH9fFRUhLBtHQAVJaKWhrIgVnNtwGOmGC3o82YQ45qnEc6UPwP9N5h9bgo3VIv1sHEXM8v2lzj3XUY_TzGR4QRqohaOv8BH8a4gvybIAx4svLeUO-frj9cror7j9__HR6f1_osu5S0YtKa4Bac90z2bWaG9liBT2XvWRYs1qaRiMOUmNTCamFMNuqWs6MLquhvCFv9945-B8LxqQmG7cJwKFfoqq7spQ1bzN43EGd_xMDDmoOdoKwKs7U5kRtTtTmRG1OcuD1pXnpJzT_4LuEDLy5ABA1jEMAp238ywlZlbzOWLtjmNfwaDGoqC06jcaGbEoZb_83wm8H3qyx</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>69335618</pqid></control><display><type>article</type><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><source>ScienceDirect Freedom Collection</source><creator>Joubert, A.M. ; Panzer, A. ; Joubert, F. ; Lottering, M.-L. ; Bianchi, P.C. ; Seegers, J.C.</creator><creatorcontrib>Joubert, A.M. ; Panzer, A. ; Joubert, F. ; Lottering, M.-L. ; Bianchi, P.C. ; Seegers, J.C.</creatorcontrib><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.</description><identifier>ISSN: 0952-3278</identifier><identifier>EISSN: 1532-2823</identifier><identifier>DOI: 10.1054/plef.1999.0087</identifier><identifier>PMID: 10582657</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>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</subject><ispartof>Prostaglandins, leukotrienes and essential fatty acids, 1999-09, Vol.61 (3), p.171-182</ispartof><rights>1999 Harcourt Publishers Ltd</rights><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c369t-b24ccaa6c1cb0598c1d58e4ab15b50e6065d7ceef5ce7425c22d1532810dc34f3</citedby><cites>FETCH-LOGICAL-c369t-b24ccaa6c1cb0598c1d58e4ab15b50e6065d7ceef5ce7425c22d1532810dc34f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1254316$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10582657$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><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><title>Prostaglandins, leukotrienes and essential fatty acids</title><addtitle>Prostaglandins Leukot Essent Fatty Acids</addtitle><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.</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>
fulltext fulltext
identifier ISSN: 0952-3278
ispartof Prostaglandins, leukotrienes and essential fatty acids, 1999-09, Vol.61 (3), p.171-182
issn 0952-3278
1532-2823
language eng
recordid cdi_proquest_miscellaneous_69335618
source ScienceDirect Freedom Collection
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T04%3A02%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Comparative%20study%20of%20the%20effects%20of%20polyunsaturated%20fatty%20acids%20and%20their%20metabolites%20on%20cell%20growth%20and%20tyrosine%20kinase%20activity%20in%20oesophageal%20carcinoma%20cells&rft.jtitle=Prostaglandins,%20leukotrienes%20and%20essential%20fatty%20acids&rft.au=Joubert,%20A.M.&rft.date=1999-09-01&rft.volume=61&rft.issue=3&rft.spage=171&rft.epage=182&rft.pages=171-182&rft.issn=0952-3278&rft.eissn=1532-2823&rft_id=info:doi/10.1054/plef.1999.0087&rft_dat=%3Cproquest_cross%3E69335618%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c369t-b24ccaa6c1cb0598c1d58e4ab15b50e6065d7ceef5ce7425c22d1532810dc34f3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=69335618&rft_id=info:pmid/10582657&rfr_iscdi=true