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Human Carcinoma Cells Synthesize and Secrete Tenascin in vitro
Tenascin is an extracellular matrix glycoprotein produced in response to epithelial‐mesenchymal interactions that initiate fetal organogenesis, and it is also found in the stroma of benign and malignant neoplasms. Thirty‐five human cell lines representing a variety of cancers were examined by im‐mun...
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Published in: | Cancer science 1992-10, Vol.83 (10), p.1073-1080 |
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creator | Kawakatsu, Hisaaki Shiurba, Robert Obara, Masanobu Hiraiwa, Hideki Kusakabe, Moriaki Sakakura, Teruyo |
description | Tenascin is an extracellular matrix glycoprotein produced in response to epithelial‐mesenchymal interactions that initiate fetal organogenesis, and it is also found in the stroma of benign and malignant neoplasms. Thirty‐five human cell lines representing a variety of cancers were examined by im‐munoprecipitation and polyacrylamide gel electrophoresis of radiolabeled tenascin proteins from conditioned media. Two forms of tenascin with relative molecular masses of 190,000 and 250,000 were identified. Eight cell lines produced both forms. With the exception of myeloid and lymphoid leukemias and Burkitt's lymphoma, all of the mesodermal and neuroectodermal tumor lines were found to synthesize tenascin. Unexpectedly, tenascin was secreted by several mammary and colonic adenocarcinomas as well as by a line derived from normal mammary epithelial cells, and in some cases increased production was induced by transforming growth factor beta in serum‐free medium. Cells producing fibronectin but not tenascin attached and spread on plastic culture dishes, while those producing tenascin alone remained suspended in the medium or were rarely attached. Tenascin also inhibited fibronectin‐mediated adhesion of MCF7 breast carcinoma cells in vitro. The results suggest that tenascins synthesized and secreted by some cancer cells, especially those of epithelial origin, may have specific roles in determining tumor cell adhesion and ultimately the ability to form invasive outgrowths. |
doi_str_mv | 10.1111/j.1349-7006.1992.tb02724.x |
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Thirty‐five human cell lines representing a variety of cancers were examined by im‐munoprecipitation and polyacrylamide gel electrophoresis of radiolabeled tenascin proteins from conditioned media. Two forms of tenascin with relative molecular masses of 190,000 and 250,000 were identified. Eight cell lines produced both forms. With the exception of myeloid and lymphoid leukemias and Burkitt's lymphoma, all of the mesodermal and neuroectodermal tumor lines were found to synthesize tenascin. Unexpectedly, tenascin was secreted by several mammary and colonic adenocarcinomas as well as by a line derived from normal mammary epithelial cells, and in some cases increased production was induced by transforming growth factor beta in serum‐free medium. Cells producing fibronectin but not tenascin attached and spread on plastic culture dishes, while those producing tenascin alone remained suspended in the medium or were rarely attached. 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The results suggest that tenascins synthesized and secreted by some cancer cells, especially those of epithelial origin, may have specific roles in determining tumor cell adhesion and ultimately the ability to form invasive outgrowths.</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.1349-7006.1992.tb02724.x</identifier><identifier>PMID: 1280634</identifier><identifier>CODEN: GANNA2</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Animals ; Antibody Specificity ; Antigens, Neoplasm ; Biological and medical sciences ; Blotting, Western ; Breast carcinoma ; Burkitt's lymphoma ; Carcinoma - metabolism ; Cell adhesion ; Cell Adhesion - physiology ; Cell Adhesion Molecules, Neuronal - biosynthesis ; Cell Adhesion Molecules, Neuronal - physiology ; Cell culture ; Culture media ; Epithelial cells ; Epithelium - metabolism ; Extracellular matrix ; Extracellular Matrix - physiology ; Extracellular Matrix Proteins - biosynthesis ; Extracellular Matrix Proteins - physiology ; Female ; Fetuses ; Fibronectin ; Fibronectins - biosynthesis ; Gel electrophoresis ; General aspects (metabolism, cell proliferation, established cell line...) ; Growth factors ; Human carcinoma cell ; Humans ; Invasiveness ; Mammary gland ; Medical sciences ; Mesenchyme ; Neoplasia ; Neoplasm Proteins - biosynthesis ; Neoplasm Proteins - metabolism ; Neoplasms - metabolism ; Nervous system diseases ; Organogenesis ; Plastics ; Polyacrylamide ; Rats ; Stroma ; Tenascin ; Transforming growth factor-b ; Tumor cell ; Tumor Cells, Cultured ; Tumors</subject><ispartof>Cancer science, 1992-10, Vol.83 (10), p.1073-1080</ispartof><rights>1993 INIST-CNRS</rights><rights>Copyright John Wiley & Sons, Inc. 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Thirty‐five human cell lines representing a variety of cancers were examined by im‐munoprecipitation and polyacrylamide gel electrophoresis of radiolabeled tenascin proteins from conditioned media. Two forms of tenascin with relative molecular masses of 190,000 and 250,000 were identified. Eight cell lines produced both forms. With the exception of myeloid and lymphoid leukemias and Burkitt's lymphoma, all of the mesodermal and neuroectodermal tumor lines were found to synthesize tenascin. Unexpectedly, tenascin was secreted by several mammary and colonic adenocarcinomas as well as by a line derived from normal mammary epithelial cells, and in some cases increased production was induced by transforming growth factor beta in serum‐free medium. Cells producing fibronectin but not tenascin attached and spread on plastic culture dishes, while those producing tenascin alone remained suspended in the medium or were rarely attached. 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The results suggest that tenascins synthesized and secreted by some cancer cells, especially those of epithelial origin, may have specific roles in determining tumor cell adhesion and ultimately the ability to form invasive outgrowths.</description><subject>Animals</subject><subject>Antibody Specificity</subject><subject>Antigens, Neoplasm</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Breast carcinoma</subject><subject>Burkitt's lymphoma</subject><subject>Carcinoma - metabolism</subject><subject>Cell adhesion</subject><subject>Cell Adhesion - physiology</subject><subject>Cell Adhesion Molecules, Neuronal - biosynthesis</subject><subject>Cell Adhesion Molecules, Neuronal - physiology</subject><subject>Cell culture</subject><subject>Culture media</subject><subject>Epithelial cells</subject><subject>Epithelium - metabolism</subject><subject>Extracellular matrix</subject><subject>Extracellular Matrix - physiology</subject><subject>Extracellular Matrix Proteins - biosynthesis</subject><subject>Extracellular Matrix Proteins - physiology</subject><subject>Female</subject><subject>Fetuses</subject><subject>Fibronectin</subject><subject>Fibronectins - biosynthesis</subject><subject>Gel electrophoresis</subject><subject>General aspects (metabolism, cell proliferation, established cell line...)</subject><subject>Growth factors</subject><subject>Human carcinoma cell</subject><subject>Humans</subject><subject>Invasiveness</subject><subject>Mammary gland</subject><subject>Medical sciences</subject><subject>Mesenchyme</subject><subject>Neoplasia</subject><subject>Neoplasm Proteins - biosynthesis</subject><subject>Neoplasm Proteins - metabolism</subject><subject>Neoplasms - metabolism</subject><subject>Nervous system diseases</subject><subject>Organogenesis</subject><subject>Plastics</subject><subject>Polyacrylamide</subject><subject>Rats</subject><subject>Stroma</subject><subject>Tenascin</subject><subject>Transforming growth factor-b</subject><subject>Tumor cell</subject><subject>Tumor Cells, Cultured</subject><subject>Tumors</subject><issn>0910-5050</issn><issn>1347-9032</issn><issn>1349-7006</issn><issn>1876-4673</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNqVkU1v1DAQhi0EKtvCT0CKAPWWMP7IOOZQVEWFIlXi0HK2vK5DvUqcYiely6_H0a6WjxvWSD68z4zmnZeQ1xQqmt-7TUW5UKUEwIoqxappDUwyUT0-IauD9JSsQFEoa6jhOTlOaQNAJSA7IkeUNYBcrMjZ5TyYULQmWh_GwRSt6_tUXG_DdOeS_-kKE26La2ejm1xx44JJGSxyPfgpji_Is870yb3c_yfk68eLm_ayvPry6XN7flVaIRQv0aBCx8EI6ZhE5CiANXwtRe0sMtHgWlKhmo4r5F3TITeWyU4Bp40TFvkJOdvNvZ_Xg7u1LkzR9Po--sHErR6N138rwd_pb-ODrhVtEFUecLofEMfvs0uTHnyy2asJbpyTlpxLBbXI4Jt_wM04x5DNacaVqrmSSDP1fkfZOKYUXXdYhYJeMtIbvQShlyD0kpHeZ6Qfc_OrP838bt2FkvW3ez0f2_RdNMH6dMCEYIzicpMPO-yH7932PxbQ7fkFhez4FwvJrF4</recordid><startdate>199210</startdate><enddate>199210</enddate><creator>Kawakatsu, Hisaaki</creator><creator>Shiurba, Robert</creator><creator>Obara, Masanobu</creator><creator>Hiraiwa, Hideki</creator><creator>Kusakabe, Moriaki</creator><creator>Sakakura, Teruyo</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>199210</creationdate><title>Human Carcinoma Cells Synthesize and Secrete Tenascin in vitro</title><author>Kawakatsu, Hisaaki ; 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Thirty‐five human cell lines representing a variety of cancers were examined by im‐munoprecipitation and polyacrylamide gel electrophoresis of radiolabeled tenascin proteins from conditioned media. Two forms of tenascin with relative molecular masses of 190,000 and 250,000 were identified. Eight cell lines produced both forms. With the exception of myeloid and lymphoid leukemias and Burkitt's lymphoma, all of the mesodermal and neuroectodermal tumor lines were found to synthesize tenascin. Unexpectedly, tenascin was secreted by several mammary and colonic adenocarcinomas as well as by a line derived from normal mammary epithelial cells, and in some cases increased production was induced by transforming growth factor beta in serum‐free medium. Cells producing fibronectin but not tenascin attached and spread on plastic culture dishes, while those producing tenascin alone remained suspended in the medium or were rarely attached. Tenascin also inhibited fibronectin‐mediated adhesion of MCF7 breast carcinoma cells in vitro. The results suggest that tenascins synthesized and secreted by some cancer cells, especially those of epithelial origin, may have specific roles in determining tumor cell adhesion and ultimately the ability to form invasive outgrowths.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>1280634</pmid><doi>10.1111/j.1349-7006.1992.tb02724.x</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antibody Specificity Antigens, Neoplasm Biological and medical sciences Blotting, Western Breast carcinoma Burkitt's lymphoma Carcinoma - metabolism Cell adhesion Cell Adhesion - physiology Cell Adhesion Molecules, Neuronal - biosynthesis Cell Adhesion Molecules, Neuronal - physiology Cell culture Culture media Epithelial cells Epithelium - metabolism Extracellular matrix Extracellular Matrix - physiology Extracellular Matrix Proteins - biosynthesis Extracellular Matrix Proteins - physiology Female Fetuses Fibronectin Fibronectins - biosynthesis Gel electrophoresis General aspects (metabolism, cell proliferation, established cell line...) Growth factors Human carcinoma cell Humans Invasiveness Mammary gland Medical sciences Mesenchyme Neoplasia Neoplasm Proteins - biosynthesis Neoplasm Proteins - metabolism Neoplasms - metabolism Nervous system diseases Organogenesis Plastics Polyacrylamide Rats Stroma Tenascin Transforming growth factor-b Tumor cell Tumor Cells, Cultured Tumors |
title | Human Carcinoma Cells Synthesize and Secrete Tenascin in vitro |
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