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Cytokine Profile of Cervical Cancer Cells
Objective. In patients with cervical carcinoma, the presence of cytokines produced by TH2 cells, and the presence of an eosinophilic inflammatory infiltrate, has been associated with a less effective immune response and tumor progression. In the present study, we have investigated the cytokine profi...
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Published in: | Gynecologic oncology 2001-11, Vol.83 (2), p.235-243 |
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creator | Hazelbag, Suzanne Fleuren, Gert Jan Baelde, J.J. Schuuring, Ed Kenter, Gemma G. Gorter, Arko |
description | Objective. In patients with cervical carcinoma, the presence of cytokines produced by TH2 cells, and the presence of an eosinophilic inflammatory infiltrate, has been associated with a less effective immune response and tumor progression. In the present study, we have investigated the cytokine profile of cervical carcinoma cells. In addition, we have measured whether differences in cytokine profiles between normal and malignant cervical epithelial cells are present.
Methods. For this purpose we have determined the mRNA expression patterns of 20 relevant cytokines by RT-PCR and Southern blotting in 3 normal primary cervical epithelial cell cultures (NPE) and 10 cervical cancer cell lines (CCCL).
Results. TGF-β1, IL-4, IL-12p35, and IL-15 were produced by all CCCL and NPE. TNF-α, IL-10, IL-5, and RANTES were present in most NPE, but not in any of the CCCL. MCP-1 was expressed in all CCCL but in only one NPE. The presence of the anti-inflammatory cytokine TGF-β1 in cervical carcinomas was confirmed by RNA in situ hybridization on tissue sections of carcinomas from which the CCCL originated.
Conclusions. Our results suggest that cervical carcinoma cells produce immunomodulatory cytokines and that cytokine expression patterns change after malignant transformation. The implications of locally produced cytokines by cervical cancer cells are further discussed. |
doi_str_mv | 10.1006/gyno.2001.6378 |
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Methods. For this purpose we have determined the mRNA expression patterns of 20 relevant cytokines by RT-PCR and Southern blotting in 3 normal primary cervical epithelial cell cultures (NPE) and 10 cervical cancer cell lines (CCCL).
Results. TGF-β1, IL-4, IL-12p35, and IL-15 were produced by all CCCL and NPE. TNF-α, IL-10, IL-5, and RANTES were present in most NPE, but not in any of the CCCL. MCP-1 was expressed in all CCCL but in only one NPE. The presence of the anti-inflammatory cytokine TGF-β1 in cervical carcinomas was confirmed by RNA in situ hybridization on tissue sections of carcinomas from which the CCCL originated.
Conclusions. Our results suggest that cervical carcinoma cells produce immunomodulatory cytokines and that cytokine expression patterns change after malignant transformation. The implications of locally produced cytokines by cervical cancer cells are further discussed.</description><identifier>ISSN: 0090-8258</identifier><identifier>EISSN: 1095-6859</identifier><identifier>DOI: 10.1006/gyno.2001.6378</identifier><identifier>PMID: 11606077</identifier><identifier>CODEN: GYNOA3</identifier><language>eng</language><publisher>San Diego, CA: Elsevier Inc</publisher><subject>Biological and medical sciences ; Blotting, Southern ; Cell Transformation, Neoplastic - genetics ; Cell Transformation, Neoplastic - immunology ; Cell Transformation, Neoplastic - metabolism ; cervix cancer cytokines ; Cytokines - biosynthesis ; Cytokines - genetics ; Cytokines - immunology ; Female ; Female genital diseases ; Gene Expression Profiling ; Gene Expression Regulation, Neoplastic ; Gynecology. Andrology. Obstetrics ; HeLa Cells ; Humans ; Medical sciences ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - biosynthesis ; RNA, Messenger - genetics ; Tumor Cells, Cultured ; Tumors ; Uterine Cervical Neoplasms - genetics ; Uterine Cervical Neoplasms - immunology ; Uterine Cervical Neoplasms - metabolism</subject><ispartof>Gynecologic oncology, 2001-11, Vol.83 (2), p.235-243</ispartof><rights>2001 Academic Press</rights><rights>2002 INIST-CNRS</rights><rights>Copyright 2001 Academic Press.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-460c4d5146398dfd68a43f2067766163922375e780f6e30c232c73946b0f98703</citedby><cites>FETCH-LOGICAL-c370t-460c4d5146398dfd68a43f2067766163922375e780f6e30c232c73946b0f98703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14158608$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11606077$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hazelbag, Suzanne</creatorcontrib><creatorcontrib>Fleuren, Gert Jan</creatorcontrib><creatorcontrib>Baelde, J.J.</creatorcontrib><creatorcontrib>Schuuring, Ed</creatorcontrib><creatorcontrib>Kenter, Gemma G.</creatorcontrib><creatorcontrib>Gorter, Arko</creatorcontrib><title>Cytokine Profile of Cervical Cancer Cells</title><title>Gynecologic oncology</title><addtitle>Gynecol Oncol</addtitle><description>Objective. In patients with cervical carcinoma, the presence of cytokines produced by TH2 cells, and the presence of an eosinophilic inflammatory infiltrate, has been associated with a less effective immune response and tumor progression. In the present study, we have investigated the cytokine profile of cervical carcinoma cells. In addition, we have measured whether differences in cytokine profiles between normal and malignant cervical epithelial cells are present.
Methods. For this purpose we have determined the mRNA expression patterns of 20 relevant cytokines by RT-PCR and Southern blotting in 3 normal primary cervical epithelial cell cultures (NPE) and 10 cervical cancer cell lines (CCCL).
Results. TGF-β1, IL-4, IL-12p35, and IL-15 were produced by all CCCL and NPE. TNF-α, IL-10, IL-5, and RANTES were present in most NPE, but not in any of the CCCL. MCP-1 was expressed in all CCCL but in only one NPE. The presence of the anti-inflammatory cytokine TGF-β1 in cervical carcinomas was confirmed by RNA in situ hybridization on tissue sections of carcinomas from which the CCCL originated.
Conclusions. Our results suggest that cervical carcinoma cells produce immunomodulatory cytokines and that cytokine expression patterns change after malignant transformation. The implications of locally produced cytokines by cervical cancer cells are further discussed.</description><subject>Biological and medical sciences</subject><subject>Blotting, Southern</subject><subject>Cell Transformation, Neoplastic - genetics</subject><subject>Cell Transformation, Neoplastic - immunology</subject><subject>Cell Transformation, Neoplastic - metabolism</subject><subject>cervix cancer cytokines</subject><subject>Cytokines - biosynthesis</subject><subject>Cytokines - genetics</subject><subject>Cytokines - immunology</subject><subject>Female</subject><subject>Female genital diseases</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - biosynthesis</subject><subject>RNA, Messenger - genetics</subject><subject>Tumor Cells, Cultured</subject><subject>Tumors</subject><subject>Uterine Cervical Neoplasms - genetics</subject><subject>Uterine Cervical Neoplasms - immunology</subject><subject>Uterine Cervical Neoplasms - metabolism</subject><issn>0090-8258</issn><issn>1095-6859</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNp1kE1LxDAQhoMo7rp69Si9KHhonSRtkh6l-AULetBzyKaJRLvNmnQX9t-bsgVPnoYZnnmZeRC6xFBgAHb3ue99QQBwwSgXR2iOoa5yJqr6GM0BasgFqcQMncX4BQAUMDlFM4wZMOB8jm6b_eC_XW-yt-Ct60zmbdaYsHNadVmjem1C6rsunqMTq7poLqa6QB-PD-_Nc758fXpp7pe5phyGvGSgy7bCJaO1aG3LhCqpJcA4ZwynISGUV4YLsMxQ0IQSzWldshXYWnCgC3RzyN0E_7M1cZBrF3W6QPXGb6PkhACvME5gcQB18DEGY-UmuLUKe4lBjnLkKEeOcuQoJy1cTcnb1dq0f_hkIwHXE6Biet-G9L6Lf1yJK8FgDBIHziQPO2eCjNqZpKp1wehBtt79d8MvPxl8iA</recordid><startdate>20011101</startdate><enddate>20011101</enddate><creator>Hazelbag, Suzanne</creator><creator>Fleuren, Gert Jan</creator><creator>Baelde, J.J.</creator><creator>Schuuring, Ed</creator><creator>Kenter, Gemma G.</creator><creator>Gorter, Arko</creator><general>Elsevier Inc</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>20011101</creationdate><title>Cytokine Profile of Cervical Cancer Cells</title><author>Hazelbag, Suzanne ; Fleuren, Gert Jan ; Baelde, J.J. ; Schuuring, Ed ; Kenter, Gemma G. ; Gorter, Arko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-460c4d5146398dfd68a43f2067766163922375e780f6e30c232c73946b0f98703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Biological and medical sciences</topic><topic>Blotting, Southern</topic><topic>Cell Transformation, Neoplastic - genetics</topic><topic>Cell Transformation, Neoplastic - immunology</topic><topic>Cell Transformation, Neoplastic - metabolism</topic><topic>cervix cancer cytokines</topic><topic>Cytokines - biosynthesis</topic><topic>Cytokines - genetics</topic><topic>Cytokines - immunology</topic><topic>Female</topic><topic>Female genital diseases</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - biosynthesis</topic><topic>RNA, Messenger - genetics</topic><topic>Tumor Cells, Cultured</topic><topic>Tumors</topic><topic>Uterine Cervical Neoplasms - genetics</topic><topic>Uterine Cervical Neoplasms - immunology</topic><topic>Uterine Cervical Neoplasms - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hazelbag, Suzanne</creatorcontrib><creatorcontrib>Fleuren, Gert Jan</creatorcontrib><creatorcontrib>Baelde, J.J.</creatorcontrib><creatorcontrib>Schuuring, Ed</creatorcontrib><creatorcontrib>Kenter, Gemma G.</creatorcontrib><creatorcontrib>Gorter, Arko</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>Gynecologic oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hazelbag, Suzanne</au><au>Fleuren, Gert Jan</au><au>Baelde, J.J.</au><au>Schuuring, Ed</au><au>Kenter, Gemma G.</au><au>Gorter, Arko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cytokine Profile of Cervical Cancer Cells</atitle><jtitle>Gynecologic oncology</jtitle><addtitle>Gynecol Oncol</addtitle><date>2001-11-01</date><risdate>2001</risdate><volume>83</volume><issue>2</issue><spage>235</spage><epage>243</epage><pages>235-243</pages><issn>0090-8258</issn><eissn>1095-6859</eissn><coden>GYNOA3</coden><abstract>Objective. In patients with cervical carcinoma, the presence of cytokines produced by TH2 cells, and the presence of an eosinophilic inflammatory infiltrate, has been associated with a less effective immune response and tumor progression. In the present study, we have investigated the cytokine profile of cervical carcinoma cells. In addition, we have measured whether differences in cytokine profiles between normal and malignant cervical epithelial cells are present.
Methods. For this purpose we have determined the mRNA expression patterns of 20 relevant cytokines by RT-PCR and Southern blotting in 3 normal primary cervical epithelial cell cultures (NPE) and 10 cervical cancer cell lines (CCCL).
Results. TGF-β1, IL-4, IL-12p35, and IL-15 were produced by all CCCL and NPE. TNF-α, IL-10, IL-5, and RANTES were present in most NPE, but not in any of the CCCL. MCP-1 was expressed in all CCCL but in only one NPE. The presence of the anti-inflammatory cytokine TGF-β1 in cervical carcinomas was confirmed by RNA in situ hybridization on tissue sections of carcinomas from which the CCCL originated.
Conclusions. Our results suggest that cervical carcinoma cells produce immunomodulatory cytokines and that cytokine expression patterns change after malignant transformation. The implications of locally produced cytokines by cervical cancer cells are further discussed.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>11606077</pmid><doi>10.1006/gyno.2001.6378</doi><tpages>9</tpages></addata></record> |
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subjects | Biological and medical sciences Blotting, Southern Cell Transformation, Neoplastic - genetics Cell Transformation, Neoplastic - immunology Cell Transformation, Neoplastic - metabolism cervix cancer cytokines Cytokines - biosynthesis Cytokines - genetics Cytokines - immunology Female Female genital diseases Gene Expression Profiling Gene Expression Regulation, Neoplastic Gynecology. Andrology. Obstetrics HeLa Cells Humans Medical sciences Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - biosynthesis RNA, Messenger - genetics Tumor Cells, Cultured Tumors Uterine Cervical Neoplasms - genetics Uterine Cervical Neoplasms - immunology Uterine Cervical Neoplasms - metabolism |
title | Cytokine Profile of Cervical Cancer Cells |
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