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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
Main Authors: Kawakatsu, Hisaaki, Shiurba, Robert, Obara, Masanobu, Hiraiwa, Hideki, Kusakabe, Moriaki, Sakakura, Teruyo
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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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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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identifier ISSN: 0910-5050
ispartof Cancer science, 1992-10, Vol.83 (10), p.1073-1080
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source Publicly Available Content Database; PubMed Central
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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