Fas (CD95) expression is up-regulated on papillary thyroid carcinoma

Thyrocyte apoptosis signaled through the Fas receptor has been proposed as a mechanism for the cytotoxicity observed in thyroiditis, but the role the Fas pathway plays in thyroid cancer is not known. We examined Fas expression in thyroid tissue derived from patients with papillary carcinoma and foll...

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Veröffentlicht in:The journal of clinical endocrinology and metabolism 1999-11, Vol.84 (11), p.4246-4252
Hauptverfasser: ARSCOTT, P. L, STOKES, T, MYC, A, GIORDANO, T. J, THOMPSON, N. W, BAKER, J. R
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container_end_page 4252
container_issue 11
container_start_page 4246
container_title The journal of clinical endocrinology and metabolism
container_volume 84
creator ARSCOTT, P. L
STOKES, T
MYC, A
GIORDANO, T. J
THOMPSON, N. W
BAKER, J. R
description Thyrocyte apoptosis signaled through the Fas receptor has been proposed as a mechanism for the cytotoxicity observed in thyroiditis, but the role the Fas pathway plays in thyroid cancer is not known. We examined Fas expression in thyroid tissue derived from patients with papillary carcinoma and follicular cancer. More intense immunohistological staining for the Fas protein was observed on papillary cancer cells as compared with adjacent normal follicles. To further characterize the expression of Fas in papillary cancer, paired normal and cancerous thyroid tissues were obtained at thyroidectomy from several donors, digested, and placed into cell culture. Messenger RNA was analyzed by ribonuclease protection assays, and protein was identified by flow cytometry. Fas expression was detected at levels up to 3-fold higher in cancerous thyrocytes compared with paired normal cells. To determine whether the expressed Fas antigen was functional, thyrocytes were treated with a monoclonal IgM anti-Fas antibody (clone CH11; Upstate Biotechnology, Inc., Lake Placid, NY) in the presence of interferon-gamma and cycloheximide. Whereas both normal and cancerous thyrocytes were induced to die after this treatment, the cancerous thyrocytes were more sensitive to anti-Fas antibody. This work demonstrates that the Fas antigen is expressed and functional on papillary thyroid cancer cells and this may have potential therapeutic significance.
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Fas expression was detected at levels up to 3-fold higher in cancerous thyrocytes compared with paired normal cells. To determine whether the expressed Fas antigen was functional, thyrocytes were treated with a monoclonal IgM anti-Fas antibody (clone CH11; Upstate Biotechnology, Inc., Lake Placid, NY) in the presence of interferon-gamma and cycloheximide. Whereas both normal and cancerous thyrocytes were induced to die after this treatment, the cancerous thyrocytes were more sensitive to anti-Fas antibody. 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R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fas (CD95) expression is up-regulated on papillary thyroid carcinoma</atitle><jtitle>The journal of clinical endocrinology and metabolism</jtitle><addtitle>J Clin Endocrinol Metab</addtitle><date>1999-11-01</date><risdate>1999</risdate><volume>84</volume><issue>11</issue><spage>4246</spage><epage>4252</epage><pages>4246-4252</pages><issn>0021-972X</issn><eissn>1945-7197</eissn><coden>JCEMAZ</coden><abstract>Thyrocyte apoptosis signaled through the Fas receptor has been proposed as a mechanism for the cytotoxicity observed in thyroiditis, but the role the Fas pathway plays in thyroid cancer is not known. We examined Fas expression in thyroid tissue derived from patients with papillary carcinoma and follicular cancer. More intense immunohistological staining for the Fas protein was observed on papillary cancer cells as compared with adjacent normal follicles. To further characterize the expression of Fas in papillary cancer, paired normal and cancerous thyroid tissues were obtained at thyroidectomy from several donors, digested, and placed into cell culture. Messenger RNA was analyzed by ribonuclease protection assays, and protein was identified by flow cytometry. Fas expression was detected at levels up to 3-fold higher in cancerous thyrocytes compared with paired normal cells. To determine whether the expressed Fas antigen was functional, thyrocytes were treated with a monoclonal IgM anti-Fas antibody (clone CH11; Upstate Biotechnology, Inc., Lake Placid, NY) in the presence of interferon-gamma and cycloheximide. Whereas both normal and cancerous thyrocytes were induced to die after this treatment, the cancerous thyrocytes were more sensitive to anti-Fas antibody. 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subjects Adenocarcinoma, Follicular - immunology
Antibodies, Monoclonal - pharmacology
Apoptosis
Biological and medical sciences
Carcinoma, Papillary - immunology
Endocrinopathies
fas Receptor - analysis
fas Receptor - genetics
fas Receptor - physiology
Flow Cytometry
Gene Expression Regulation, Neoplastic
Humans
Immunoglobulin M - pharmacology
Immunohistochemistry
Malignant tumors
Medical sciences
RNA, Messenger - analysis
Thyroid Neoplasms - immunology
Thyroid. Thyroid axis (diseases)
title Fas (CD95) expression is up-regulated on papillary thyroid carcinoma
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