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...

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Veröffentlicht in:Cancer science 1994-02, Vol.85 (2), p.179-186
Hauptverfasser: Mizuno, Kazuto, Sone, Saburo, Orino, Etsuko, Nii, Akihiko, Ogura, Takeshi
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container_issue 2
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container_title Cancer science
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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
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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. 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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 - 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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 - 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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>
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identifier ISSN: 0910-5050
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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
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