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Quantitation of autoantibodies to cytokeratins in sera from patients with squamous cell carcinoma of the oesophagus.

Sera drawn from healthy individuals, patients with squamous cell carcinoma (SCC) of the oesophagus and patients with mild active oesophagitis were examined for autoantibodies to cytoskeletal proteins extracted from the normal oesophageal keratinocyte or from 2 carcinoma cell lines, each of the latte...

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Autores principales: Veale, R. B., Thornley, A. L., Scott, E., Antoni, A., Segal, I.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1988
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246860/
https://www.ncbi.nlm.nih.gov/pubmed/2465018
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author Veale, R. B.
Thornley, A. L.
Scott, E.
Antoni, A.
Segal, I.
author_facet Veale, R. B.
Thornley, A. L.
Scott, E.
Antoni, A.
Segal, I.
author_sort Veale, R. B.
collection PubMed
description Sera drawn from healthy individuals, patients with squamous cell carcinoma (SCC) of the oesophagus and patients with mild active oesophagitis were examined for autoantibodies to cytoskeletal proteins extracted from the normal oesophageal keratinocyte or from 2 carcinoma cell lines, each of the latter have a simple cytoskeleton. Using a radioimmunoassay with normal oesophageal cytokeratins as bound antigen, 86 normal, 76 SCC and 14 oesophagitis sera were compared. No significant difference in autoantibody titre was found. When the bound antigen was changed to one containing predominantly simple epithelial cytokeratins a significant increase (32% P less than 0.001) was noted in the SCC category only. Western blots using simple epithelial cell extracts as antigen revealed autoantibodies to cytokeratins 8, 18 and 19 as well as to one other unidentified protein in most SCC sera, and in some normal sera. Antibodies to cytokeratin 18 predominated. Normal and SCC sera were applied using indirect immunofluorescent techniques to normal oesophageal keratinocytes, SNO oesophageal SCC cells and HeLa cells grown in vitro. Autoantibodies to oesophageal cytokeratins were, with few exceptions, barely detectable. Strong reactions were noted against SNO and HeLa cytoskeletal components, but also against nuclear membrane and nucleolar determinants. These experiments suggest that raised levels of autoantibodies to certain cytoskeletal and nuclear determinants may be a feature of oesophageal cancer. IMAGES:
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spelling pubmed-22468602009-09-10 Quantitation of autoantibodies to cytokeratins in sera from patients with squamous cell carcinoma of the oesophagus. Veale, R. B. Thornley, A. L. Scott, E. Antoni, A. Segal, I. Br J Cancer Research Article Sera drawn from healthy individuals, patients with squamous cell carcinoma (SCC) of the oesophagus and patients with mild active oesophagitis were examined for autoantibodies to cytoskeletal proteins extracted from the normal oesophageal keratinocyte or from 2 carcinoma cell lines, each of the latter have a simple cytoskeleton. Using a radioimmunoassay with normal oesophageal cytokeratins as bound antigen, 86 normal, 76 SCC and 14 oesophagitis sera were compared. No significant difference in autoantibody titre was found. When the bound antigen was changed to one containing predominantly simple epithelial cytokeratins a significant increase (32% P less than 0.001) was noted in the SCC category only. Western blots using simple epithelial cell extracts as antigen revealed autoantibodies to cytokeratins 8, 18 and 19 as well as to one other unidentified protein in most SCC sera, and in some normal sera. Antibodies to cytokeratin 18 predominated. Normal and SCC sera were applied using indirect immunofluorescent techniques to normal oesophageal keratinocytes, SNO oesophageal SCC cells and HeLa cells grown in vitro. Autoantibodies to oesophageal cytokeratins were, with few exceptions, barely detectable. Strong reactions were noted against SNO and HeLa cytoskeletal components, but also against nuclear membrane and nucleolar determinants. These experiments suggest that raised levels of autoantibodies to certain cytoskeletal and nuclear determinants may be a feature of oesophageal cancer. IMAGES: Nature Publishing Group 1988-12 /pmc/articles/PMC2246860/ /pubmed/2465018 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Veale, R. B.
Thornley, A. L.
Scott, E.
Antoni, A.
Segal, I.
Quantitation of autoantibodies to cytokeratins in sera from patients with squamous cell carcinoma of the oesophagus.
title Quantitation of autoantibodies to cytokeratins in sera from patients with squamous cell carcinoma of the oesophagus.
title_full Quantitation of autoantibodies to cytokeratins in sera from patients with squamous cell carcinoma of the oesophagus.
title_fullStr Quantitation of autoantibodies to cytokeratins in sera from patients with squamous cell carcinoma of the oesophagus.
title_full_unstemmed Quantitation of autoantibodies to cytokeratins in sera from patients with squamous cell carcinoma of the oesophagus.
title_short Quantitation of autoantibodies to cytokeratins in sera from patients with squamous cell carcinoma of the oesophagus.
title_sort quantitation of autoantibodies to cytokeratins in sera from patients with squamous cell carcinoma of the oesophagus.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246860/
https://www.ncbi.nlm.nih.gov/pubmed/2465018
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