Autonomous Expressions of Cytokine Genes by Human Lung Cancer Cells and Their Paracrine Regulation
Cell‐to‐cell interaction between tumors and host inflammatory cells is important for the subsequent cancer progression or regression. We examined the expressions of mRNAs for various proinflammatory cytokines by nine human lung cancer cell lines and the influences of cytokines on their gene expressi...
Gespeichert in:
Veröffentlicht in: | Cancer science 1994-02, Vol.85 (2), p.179-186 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 186 |
---|---|
container_issue | 2 |
container_start_page | 179 |
container_title | Cancer science |
container_volume | 85 |
creator | Mizuno, Kazuto Sone, Saburo Orino, Etsuko Nii, Akihiko Ogura, Takeshi |
description | Cell‐to‐cell interaction between tumors and host inflammatory cells is important for the subsequent cancer progression or regression. We examined the expressions of mRNAs for various proinflammatory cytokines by nine human lung cancer cell lines and the influences of cytokines on their gene expressions. The cytokines used were interleukin 1β (IL‐1β), interleukin 6 (IL‐6), tumor necrosis factor α (TNF‐α), granulocyte‐macrophage colony stimulating factor (GM‐CSF) and monocyte chemotactic and activating factor. Gene expressions of cytokines were measured by Northern blot analysis. Substantial expressions of cytokine genes were detected in several lung cancer cell lines such as RERF‐LC‐MS, RERF‐LC‐OK and VMRC‐LCD, although the levels of expression of each cytokine varied in different cell lines. Four lung cancer cell lines (RERF‐LC‐MS, RERF‐LC‐OK, A549 and YO‐88) were used to examine the effects of exogenous cytokines (IL‐1β, TNF‐α and GM‐CSF) on cytokine gene expressions by the cells. TNF‐α and IL‐1β caused significant changes in the levels of mRNA expressions of certain cytokines. Moreover, on stimulation with TNF‐α, RERF‐LC‐OK cells produced IL‐6 extracellularly. These extensive differences in the levels of gene expressions and productions of cytokines could have profound effects on the interactions between human lung cancer cells and the corresponding host cells. |
doi_str_mv | 10.1111/j.1349-7006.1994.tb02080.x |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5919428</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>76419762</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5629-1552b4b2b1cbfd7b8cbd84eae8a5f30f3cb35a41a6dbe39c08d13cb642f0f54a3</originalsourceid><addsrcrecordid>eNqVkV-L1DAUxYMo6-zqRxCCim-tN23SNj4sDGXcFQYUWZ9DkqazHdtkTFqd-fabsmX882ZeAjnnHnLPD6HXBFISz_t9SnLKkxKgSAnnNB0VZFBBenyCVmfpKVoBJ5AwYPAcXYawByAlFNkFuqgIpTnnK6TW0-isG9wU8OZ48CaEztmAXYvr0-i-d9bgG2NNwOqEb6dBWryd7A7X0mrjcW36PmBpG3x3bzqPv0gvtZ-Hvprd1Msxhr1Az1rZB_Nyua_Qt4-bu_o22X6--VSvt4lmRcYTwlimqMoU0aptSlVp1VTUSFNJ1ubQ5lrlTFIii0aZnGuoGhLfCpq10DIq8yt0_Zh7mNRgGm3s6GUvDr4bpD8JJzvxt2K7e7FzPwXjhNOsigHvlgDvfkwmjGLogo4bSmtiP6IsKOFlkUXjm3-Mezd5G5cTWWw1VlwWEF0fHl3auxC8ac9fISBmjmIvZlhihiVmjmLhKI5x-NWfy5xHF3BRf7voMmjZtz7y6MLZRoHF1PJ3J7-63pz-4wOiXm9IyfMH1wq8Dg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2399062760</pqid></control><display><type>article</type><title>Autonomous Expressions of Cytokine Genes by Human Lung Cancer Cells and Their Paracrine Regulation</title><source>MEDLINE</source><source>Wiley Online Library Journals</source><source>IngentaConnect Open Access</source><source>PubMed Central</source><source>EZB Electronic Journals Library</source><creator>Mizuno, Kazuto ; Sone, Saburo ; Orino, Etsuko ; Nii, Akihiko ; Ogura, Takeshi</creator><creatorcontrib>Mizuno, Kazuto ; Sone, Saburo ; Orino, Etsuko ; Nii, Akihiko ; Ogura, Takeshi</creatorcontrib><description>Cell‐to‐cell interaction between tumors and host inflammatory cells is important for the subsequent cancer progression or regression. We examined the expressions of mRNAs for various proinflammatory cytokines by nine human lung cancer cell lines and the influences of cytokines on their gene expressions. The cytokines used were interleukin 1β (IL‐1β), interleukin 6 (IL‐6), tumor necrosis factor α (TNF‐α), granulocyte‐macrophage colony stimulating factor (GM‐CSF) and monocyte chemotactic and activating factor. Gene expressions of cytokines were measured by Northern blot analysis. Substantial expressions of cytokine genes were detected in several lung cancer cell lines such as RERF‐LC‐MS, RERF‐LC‐OK and VMRC‐LCD, although the levels of expression of each cytokine varied in different cell lines. Four lung cancer cell lines (RERF‐LC‐MS, RERF‐LC‐OK, A549 and YO‐88) were used to examine the effects of exogenous cytokines (IL‐1β, TNF‐α and GM‐CSF) on cytokine gene expressions by the cells. TNF‐α and IL‐1β caused significant changes in the levels of mRNA expressions of certain cytokines. Moreover, on stimulation with TNF‐α, RERF‐LC‐OK cells produced IL‐6 extracellularly. These extensive differences in the levels of gene expressions and productions of cytokines could have profound effects on the interactions between human lung cancer cells and the corresponding host cells.</description><identifier>ISSN: 0910-5050</identifier><identifier>ISSN: 1347-9032</identifier><identifier>EISSN: 1349-7006</identifier><identifier>EISSN: 1876-4673</identifier><identifier>DOI: 10.1111/j.1349-7006.1994.tb02080.x</identifier><identifier>PMID: 8144399</identifier><identifier>CODEN: GANNA2</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adenocarcinoma - genetics ; Adenocarcinoma - immunology ; Adenocarcinoma - metabolism ; Aged ; Autoradiography ; Biological and medical sciences ; Blotting, Northern ; Carcinoma, Small Cell - genetics ; Carcinoma, Small Cell - immunology ; Carcinoma, Small Cell - metabolism ; Cerebrospinal fluid ; Chemokine CCL2 ; Chemotactic Factors - biosynthesis ; Chemotactic Factors - genetics ; Colony-stimulating factor ; Cytokine ; Cytokines - biosynthesis ; Cytokines - genetics ; Cytokines - immunology ; Gene Expression Regulation, Neoplastic ; Granulocyte-Macrophage Colony-Stimulating Factor - biosynthesis ; Granulocyte-Macrophage Colony-Stimulating Factor - genetics ; Humans ; IL‐1, Paracrine ; Inflammation ; Interleukin 6 ; Interleukin-1 - biosynthesis ; Interleukin-1 - genetics ; Interleukin-1 - pharmacology ; Interleukin-6 - biosynthesis ; Interleukin-6 - genetics ; Leukocytes (granulocytic) ; Lung cancer ; Lung Neoplasms - genetics ; Lung Neoplasms - immunology ; Lung Neoplasms - metabolism ; Lymphocytes, Tumor-Infiltrating - immunology ; Macrophages ; Macrophages - metabolism ; Male ; Medical sciences ; Middle Aged ; Monocyte chemoattractant protein 1 ; Monocytes ; mRNA ; Paracrine signalling ; Pneumology ; Receptors, Granulocyte Colony-Stimulating Factor ; RNA, Messenger - analysis ; TNF‐α ; Tumor cell lines ; Tumor Cells, Cultured - immunology ; Tumor Cells, Cultured - metabolism ; Tumor Necrosis Factor-alpha - biosynthesis ; Tumor Necrosis Factor-alpha - genetics ; Tumor Necrosis Factor-alpha - pharmacology ; Tumor necrosis factor-TNF ; Tumor necrosis factor-α ; Tumors of the respiratory system and mediastinum ; Up-Regulation</subject><ispartof>Cancer science, 1994-02, Vol.85 (2), p.179-186</ispartof><rights>1994 INIST-CNRS</rights><rights>Copyright John Wiley & Sons, Inc. Feb 1994</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5629-1552b4b2b1cbfd7b8cbd84eae8a5f30f3cb35a41a6dbe39c08d13cb642f0f54a3</citedby><cites>FETCH-LOGICAL-c5629-1552b4b2b1cbfd7b8cbd84eae8a5f30f3cb35a41a6dbe39c08d13cb642f0f54a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919428/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919428/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,1416,27923,27924,45573,45574,53790,53792</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4057007$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8144399$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mizuno, Kazuto</creatorcontrib><creatorcontrib>Sone, Saburo</creatorcontrib><creatorcontrib>Orino, Etsuko</creatorcontrib><creatorcontrib>Nii, Akihiko</creatorcontrib><creatorcontrib>Ogura, Takeshi</creatorcontrib><title>Autonomous Expressions of Cytokine Genes by Human Lung Cancer Cells and Their Paracrine Regulation</title><title>Cancer science</title><addtitle>Jpn J Cancer Res</addtitle><description>Cell‐to‐cell interaction between tumors and host inflammatory cells is important for the subsequent cancer progression or regression. We examined the expressions of mRNAs for various proinflammatory cytokines by nine human lung cancer cell lines and the influences of cytokines on their gene expressions. The cytokines used were interleukin 1β (IL‐1β), interleukin 6 (IL‐6), tumor necrosis factor α (TNF‐α), granulocyte‐macrophage colony stimulating factor (GM‐CSF) and monocyte chemotactic and activating factor. Gene expressions of cytokines were measured by Northern blot analysis. Substantial expressions of cytokine genes were detected in several lung cancer cell lines such as RERF‐LC‐MS, RERF‐LC‐OK and VMRC‐LCD, although the levels of expression of each cytokine varied in different cell lines. Four lung cancer cell lines (RERF‐LC‐MS, RERF‐LC‐OK, A549 and YO‐88) were used to examine the effects of exogenous cytokines (IL‐1β, TNF‐α and GM‐CSF) on cytokine gene expressions by the cells. TNF‐α and IL‐1β caused significant changes in the levels of mRNA expressions of certain cytokines. Moreover, on stimulation with TNF‐α, RERF‐LC‐OK cells produced IL‐6 extracellularly. These extensive differences in the levels of gene expressions and productions of cytokines could have profound effects on the interactions between human lung cancer cells and the corresponding host cells.</description><subject>Adenocarcinoma - genetics</subject><subject>Adenocarcinoma - immunology</subject><subject>Adenocarcinoma - metabolism</subject><subject>Aged</subject><subject>Autoradiography</subject><subject>Biological and medical sciences</subject><subject>Blotting, Northern</subject><subject>Carcinoma, Small Cell - genetics</subject><subject>Carcinoma, Small Cell - immunology</subject><subject>Carcinoma, Small Cell - metabolism</subject><subject>Cerebrospinal fluid</subject><subject>Chemokine CCL2</subject><subject>Chemotactic Factors - biosynthesis</subject><subject>Chemotactic Factors - genetics</subject><subject>Colony-stimulating factor</subject><subject>Cytokine</subject><subject>Cytokines - biosynthesis</subject><subject>Cytokines - genetics</subject><subject>Cytokines - immunology</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Granulocyte-Macrophage Colony-Stimulating Factor - biosynthesis</subject><subject>Granulocyte-Macrophage Colony-Stimulating Factor - genetics</subject><subject>Humans</subject><subject>IL‐1, Paracrine</subject><subject>Inflammation</subject><subject>Interleukin 6</subject><subject>Interleukin-1 - biosynthesis</subject><subject>Interleukin-1 - genetics</subject><subject>Interleukin-1 - pharmacology</subject><subject>Interleukin-6 - biosynthesis</subject><subject>Interleukin-6 - genetics</subject><subject>Leukocytes (granulocytic)</subject><subject>Lung cancer</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - immunology</subject><subject>Lung Neoplasms - metabolism</subject><subject>Lymphocytes, Tumor-Infiltrating - immunology</subject><subject>Macrophages</subject><subject>Macrophages - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Monocyte chemoattractant protein 1</subject><subject>Monocytes</subject><subject>mRNA</subject><subject>Paracrine signalling</subject><subject>Pneumology</subject><subject>Receptors, Granulocyte Colony-Stimulating Factor</subject><subject>RNA, Messenger - analysis</subject><subject>TNF‐α</subject><subject>Tumor cell lines</subject><subject>Tumor Cells, Cultured - immunology</subject><subject>Tumor Cells, Cultured - metabolism</subject><subject>Tumor Necrosis Factor-alpha - biosynthesis</subject><subject>Tumor Necrosis Factor-alpha - genetics</subject><subject>Tumor Necrosis Factor-alpha - pharmacology</subject><subject>Tumor necrosis factor-TNF</subject><subject>Tumor necrosis factor-α</subject><subject>Tumors of the respiratory system and mediastinum</subject><subject>Up-Regulation</subject><issn>0910-5050</issn><issn>1347-9032</issn><issn>1349-7006</issn><issn>1876-4673</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqVkV-L1DAUxYMo6-zqRxCCim-tN23SNj4sDGXcFQYUWZ9DkqazHdtkTFqd-fabsmX882ZeAjnnHnLPD6HXBFISz_t9SnLKkxKgSAnnNB0VZFBBenyCVmfpKVoBJ5AwYPAcXYawByAlFNkFuqgIpTnnK6TW0-isG9wU8OZ48CaEztmAXYvr0-i-d9bgG2NNwOqEb6dBWryd7A7X0mrjcW36PmBpG3x3bzqPv0gvtZ-Hvprd1Msxhr1Az1rZB_Nyua_Qt4-bu_o22X6--VSvt4lmRcYTwlimqMoU0aptSlVp1VTUSFNJ1ubQ5lrlTFIii0aZnGuoGhLfCpq10DIq8yt0_Zh7mNRgGm3s6GUvDr4bpD8JJzvxt2K7e7FzPwXjhNOsigHvlgDvfkwmjGLogo4bSmtiP6IsKOFlkUXjm3-Mezd5G5cTWWw1VlwWEF0fHl3auxC8ac9fISBmjmIvZlhihiVmjmLhKI5x-NWfy5xHF3BRf7voMmjZtz7y6MLZRoHF1PJ3J7-63pz-4wOiXm9IyfMH1wq8Dg</recordid><startdate>199402</startdate><enddate>199402</enddate><creator>Mizuno, Kazuto</creator><creator>Sone, Saburo</creator><creator>Orino, Etsuko</creator><creator>Nii, Akihiko</creator><creator>Ogura, Takeshi</creator><general>Blackwell Publishing Ltd</general><general>Japanese Cancer Association</general><general>John Wiley & Sons, Inc</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>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>199402</creationdate><title>Autonomous Expressions of Cytokine Genes by Human Lung Cancer Cells and Their Paracrine Regulation</title><author>Mizuno, Kazuto ; Sone, Saburo ; Orino, Etsuko ; Nii, Akihiko ; Ogura, Takeshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5629-1552b4b2b1cbfd7b8cbd84eae8a5f30f3cb35a41a6dbe39c08d13cb642f0f54a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Adenocarcinoma - genetics</topic><topic>Adenocarcinoma - immunology</topic><topic>Adenocarcinoma - metabolism</topic><topic>Aged</topic><topic>Autoradiography</topic><topic>Biological and medical sciences</topic><topic>Blotting, Northern</topic><topic>Carcinoma, Small Cell - genetics</topic><topic>Carcinoma, Small Cell - immunology</topic><topic>Carcinoma, Small Cell - metabolism</topic><topic>Cerebrospinal fluid</topic><topic>Chemokine CCL2</topic><topic>Chemotactic Factors - biosynthesis</topic><topic>Chemotactic Factors - genetics</topic><topic>Colony-stimulating factor</topic><topic>Cytokine</topic><topic>Cytokines - biosynthesis</topic><topic>Cytokines - genetics</topic><topic>Cytokines - immunology</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Granulocyte-Macrophage Colony-Stimulating Factor - biosynthesis</topic><topic>Granulocyte-Macrophage Colony-Stimulating Factor - genetics</topic><topic>Humans</topic><topic>IL‐1, Paracrine</topic><topic>Inflammation</topic><topic>Interleukin 6</topic><topic>Interleukin-1 - biosynthesis</topic><topic>Interleukin-1 - genetics</topic><topic>Interleukin-1 - pharmacology</topic><topic>Interleukin-6 - biosynthesis</topic><topic>Interleukin-6 - genetics</topic><topic>Leukocytes (granulocytic)</topic><topic>Lung cancer</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - immunology</topic><topic>Lung Neoplasms - metabolism</topic><topic>Lymphocytes, Tumor-Infiltrating - immunology</topic><topic>Macrophages</topic><topic>Macrophages - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Monocyte chemoattractant protein 1</topic><topic>Monocytes</topic><topic>mRNA</topic><topic>Paracrine signalling</topic><topic>Pneumology</topic><topic>Receptors, Granulocyte Colony-Stimulating Factor</topic><topic>RNA, Messenger - analysis</topic><topic>TNF‐α</topic><topic>Tumor cell lines</topic><topic>Tumor Cells, Cultured - immunology</topic><topic>Tumor Cells, Cultured - metabolism</topic><topic>Tumor Necrosis Factor-alpha - biosynthesis</topic><topic>Tumor Necrosis Factor-alpha - genetics</topic><topic>Tumor Necrosis Factor-alpha - pharmacology</topic><topic>Tumor necrosis factor-TNF</topic><topic>Tumor necrosis factor-α</topic><topic>Tumors of the respiratory system and mediastinum</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mizuno, Kazuto</creatorcontrib><creatorcontrib>Sone, Saburo</creatorcontrib><creatorcontrib>Orino, Etsuko</creatorcontrib><creatorcontrib>Nii, Akihiko</creatorcontrib><creatorcontrib>Ogura, Takeshi</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>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>Biological Sciences</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mizuno, Kazuto</au><au>Sone, Saburo</au><au>Orino, Etsuko</au><au>Nii, Akihiko</au><au>Ogura, Takeshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Autonomous Expressions of Cytokine Genes by Human Lung Cancer Cells and Their Paracrine Regulation</atitle><jtitle>Cancer science</jtitle><addtitle>Jpn J Cancer Res</addtitle><date>1994-02</date><risdate>1994</risdate><volume>85</volume><issue>2</issue><spage>179</spage><epage>186</epage><pages>179-186</pages><issn>0910-5050</issn><issn>1347-9032</issn><eissn>1349-7006</eissn><eissn>1876-4673</eissn><coden>GANNA2</coden><abstract>Cell‐to‐cell interaction between tumors and host inflammatory cells is important for the subsequent cancer progression or regression. We examined the expressions of mRNAs for various proinflammatory cytokines by nine human lung cancer cell lines and the influences of cytokines on their gene expressions. The cytokines used were interleukin 1β (IL‐1β), interleukin 6 (IL‐6), tumor necrosis factor α (TNF‐α), granulocyte‐macrophage colony stimulating factor (GM‐CSF) and monocyte chemotactic and activating factor. Gene expressions of cytokines were measured by Northern blot analysis. Substantial expressions of cytokine genes were detected in several lung cancer cell lines such as RERF‐LC‐MS, RERF‐LC‐OK and VMRC‐LCD, although the levels of expression of each cytokine varied in different cell lines. Four lung cancer cell lines (RERF‐LC‐MS, RERF‐LC‐OK, A549 and YO‐88) were used to examine the effects of exogenous cytokines (IL‐1β, TNF‐α and GM‐CSF) on cytokine gene expressions by the cells. TNF‐α and IL‐1β caused significant changes in the levels of mRNA expressions of certain cytokines. Moreover, on stimulation with TNF‐α, RERF‐LC‐OK cells produced IL‐6 extracellularly. These extensive differences in the levels of gene expressions and productions of cytokines could have profound effects on the interactions between human lung cancer cells and the corresponding host cells.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>8144399</pmid><doi>10.1111/j.1349-7006.1994.tb02080.x</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0910-5050 |
ispartof | Cancer science, 1994-02, Vol.85 (2), p.179-186 |
issn | 0910-5050 1347-9032 1349-7006 1876-4673 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5919428 |
source | MEDLINE; Wiley Online Library Journals; IngentaConnect Open Access; PubMed Central; EZB Electronic Journals Library |
subjects | Adenocarcinoma - genetics Adenocarcinoma - immunology Adenocarcinoma - metabolism Aged Autoradiography Biological and medical sciences Blotting, Northern Carcinoma, Small Cell - genetics Carcinoma, Small Cell - immunology Carcinoma, Small Cell - metabolism Cerebrospinal fluid Chemokine CCL2 Chemotactic Factors - biosynthesis Chemotactic Factors - genetics Colony-stimulating factor Cytokine Cytokines - biosynthesis Cytokines - genetics Cytokines - immunology Gene Expression Regulation, Neoplastic Granulocyte-Macrophage Colony-Stimulating Factor - biosynthesis Granulocyte-Macrophage Colony-Stimulating Factor - genetics Humans IL‐1, Paracrine Inflammation Interleukin 6 Interleukin-1 - biosynthesis Interleukin-1 - genetics Interleukin-1 - pharmacology Interleukin-6 - biosynthesis Interleukin-6 - genetics Leukocytes (granulocytic) Lung cancer Lung Neoplasms - genetics Lung Neoplasms - immunology Lung Neoplasms - metabolism Lymphocytes, Tumor-Infiltrating - immunology Macrophages Macrophages - metabolism Male Medical sciences Middle Aged Monocyte chemoattractant protein 1 Monocytes mRNA Paracrine signalling Pneumology Receptors, Granulocyte Colony-Stimulating Factor RNA, Messenger - analysis TNF‐α Tumor cell lines Tumor Cells, Cultured - immunology Tumor Cells, Cultured - metabolism Tumor Necrosis Factor-alpha - biosynthesis Tumor Necrosis Factor-alpha - genetics Tumor Necrosis Factor-alpha - pharmacology Tumor necrosis factor-TNF Tumor necrosis factor-α Tumors of the respiratory system and mediastinum Up-Regulation |
title | Autonomous Expressions of Cytokine Genes by Human Lung Cancer Cells and Their Paracrine Regulation |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T16%3A56%3A37IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Autonomous%20Expressions%20of%20Cytokine%20Genes%20by%20Human%20Lung%20Cancer%20Cells%20and%20Their%20Paracrine%20Regulation&rft.jtitle=Cancer%20science&rft.au=Mizuno,%20Kazuto&rft.date=1994-02&rft.volume=85&rft.issue=2&rft.spage=179&rft.epage=186&rft.pages=179-186&rft.issn=0910-5050&rft.eissn=1349-7006&rft.coden=GANNA2&rft_id=info:doi/10.1111/j.1349-7006.1994.tb02080.x&rft_dat=%3Cproquest_pubme%3E76419762%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2399062760&rft_id=info:pmid/8144399&rfr_iscdi=true |