Prognostic implications of CD95 receptor expression in clear cell renal carcinomas

The CD95 (Apo-1/Fas) receptor-ligand system is a key regulator of apoptosis. Down-regulation of CD95 receptor and up-regulation of CD95 ligand has been reported in a variety of human tumors and is thought to confer a selective survival advantage. To explore the relevance of the CD95 system for tumor...

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Veröffentlicht in:Human pathology 2003-02, Vol.34 (2), p.174-179
Hauptverfasser: Ramp, Uwe, Bretschneider, Uta, Ebert, Thomas, Karagiannidis, Christian, Willers, Reinhardt, Gabbert, Helmut Erich, Gerharz, Claus Dieter
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container_end_page 179
container_issue 2
container_start_page 174
container_title Human pathology
container_volume 34
creator Ramp, Uwe
Bretschneider, Uta
Ebert, Thomas
Karagiannidis, Christian
Willers, Reinhardt
Gabbert, Helmut Erich
Gerharz, Claus Dieter
description The CD95 (Apo-1/Fas) receptor-ligand system is a key regulator of apoptosis. Down-regulation of CD95 receptor and up-regulation of CD95 ligand has been reported in a variety of human tumors and is thought to confer a selective survival advantage. To explore the relevance of the CD95 system for tumor progression and prognosis in clear cell renal cell carcinomas (RCCs), we analyzed CD95 receptor and ligand expression in formalin-fixed tissue from 149 clear cell RCCs by immunohistochemistry. CD95 ligand expression could not be detected in nonneoplastic tubule epithelia and in clear cell RCCs. In contrast, CD95 receptor expression was found in the great majority of clear cell RCCs, and no down-regulation of CD95 receptor protein was evident when compared with nonneoplastic tubule epithelia. Although a significant increase (P = 0.004) of CD95 receptor expression was evident from well-differentiated (G1) to poorly differentiated (G3) RCCs, CD95 receptor expression was not correlated with tumor stage or survival of RCC patients. In conclusion, clear cell RCCs differ from other types of human cancer by their failure to down-regulate CD95 receptor expression or up-regulate CD95 ligand expression during tumor progression. These ex vivo observations suggest that down-regulation of CD95 receptor expression may not provide an additional selective growth advantage to RCC cells and thus further confirm our previous in vitro observations on a functional impairment of CD95-mediated apoptosis in RCC. HUM PATHOL 34:174-179. Copyright 2003, Elsevier Science (USA). All rights reserved.
doi_str_mv 10.1053/hupa.2003.46
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Down-regulation of CD95 receptor and up-regulation of CD95 ligand has been reported in a variety of human tumors and is thought to confer a selective survival advantage. To explore the relevance of the CD95 system for tumor progression and prognosis in clear cell renal cell carcinomas (RCCs), we analyzed CD95 receptor and ligand expression in formalin-fixed tissue from 149 clear cell RCCs by immunohistochemistry. CD95 ligand expression could not be detected in nonneoplastic tubule epithelia and in clear cell RCCs. In contrast, CD95 receptor expression was found in the great majority of clear cell RCCs, and no down-regulation of CD95 receptor protein was evident when compared with nonneoplastic tubule epithelia. Although a significant increase (P = 0.004) of CD95 receptor expression was evident from well-differentiated (G1) to poorly differentiated (G3) RCCs, CD95 receptor expression was not correlated with tumor stage or survival of RCC patients. In conclusion, clear cell RCCs differ from other types of human cancer by their failure to down-regulate CD95 receptor expression or up-regulate CD95 ligand expression during tumor progression. These ex vivo observations suggest that down-regulation of CD95 receptor expression may not provide an additional selective growth advantage to RCC cells and thus further confirm our previous in vitro observations on a functional impairment of CD95-mediated apoptosis in RCC. HUM PATHOL 34:174-179. Copyright 2003, Elsevier Science (USA). All rights reserved.</description><identifier>ISSN: 0046-8177</identifier><identifier>EISSN: 1532-8392</identifier><identifier>DOI: 10.1053/hupa.2003.46</identifier><identifier>PMID: 12612886</identifier><identifier>CODEN: HPCQA4</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adenocarcinoma, Clear Cell - chemistry ; Adenocarcinoma, Clear Cell - pathology ; Adult ; Aged ; Aged, 80 and over ; Apoptosis ; Biological and medical sciences ; CD95 receptor expression ; fas Receptor - analysis ; Female ; Humans ; Immunohistochemistry ; Kidney - chemistry ; Kidney Neoplasms - chemistry ; Kidney Neoplasms - pathology ; Kidneys ; Male ; Medical sciences ; Middle Aged ; Neoplasm Staging ; Nephrology. 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Down-regulation of CD95 receptor and up-regulation of CD95 ligand has been reported in a variety of human tumors and is thought to confer a selective survival advantage. To explore the relevance of the CD95 system for tumor progression and prognosis in clear cell renal cell carcinomas (RCCs), we analyzed CD95 receptor and ligand expression in formalin-fixed tissue from 149 clear cell RCCs by immunohistochemistry. CD95 ligand expression could not be detected in nonneoplastic tubule epithelia and in clear cell RCCs. In contrast, CD95 receptor expression was found in the great majority of clear cell RCCs, and no down-regulation of CD95 receptor protein was evident when compared with nonneoplastic tubule epithelia. Although a significant increase (P = 0.004) of CD95 receptor expression was evident from well-differentiated (G1) to poorly differentiated (G3) RCCs, CD95 receptor expression was not correlated with tumor stage or survival of RCC patients. In conclusion, clear cell RCCs differ from other types of human cancer by their failure to down-regulate CD95 receptor expression or up-regulate CD95 ligand expression during tumor progression. These ex vivo observations suggest that down-regulation of CD95 receptor expression may not provide an additional selective growth advantage to RCC cells and thus further confirm our previous in vitro observations on a functional impairment of CD95-mediated apoptosis in RCC. HUM PATHOL 34:174-179. Copyright 2003, Elsevier Science (USA). All rights reserved.</description><subject>Adenocarcinoma, Clear Cell - chemistry</subject><subject>Adenocarcinoma, Clear Cell - pathology</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Apoptosis</subject><subject>Biological and medical sciences</subject><subject>CD95 receptor expression</subject><subject>fas Receptor - analysis</subject><subject>Female</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Kidney - chemistry</subject><subject>Kidney Neoplasms - chemistry</subject><subject>Kidney Neoplasms - pathology</subject><subject>Kidneys</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neoplasm Staging</subject><subject>Nephrology. 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In conclusion, clear cell RCCs differ from other types of human cancer by their failure to down-regulate CD95 receptor expression or up-regulate CD95 ligand expression during tumor progression. These ex vivo observations suggest that down-regulation of CD95 receptor expression may not provide an additional selective growth advantage to RCC cells and thus further confirm our previous in vitro observations on a functional impairment of CD95-mediated apoptosis in RCC. HUM PATHOL 34:174-179. Copyright 2003, Elsevier Science (USA). All rights reserved.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>12612886</pmid><doi>10.1053/hupa.2003.46</doi><tpages>6</tpages></addata></record>
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subjects Adenocarcinoma, Clear Cell - chemistry
Adenocarcinoma, Clear Cell - pathology
Adult
Aged
Aged, 80 and over
Apoptosis
Biological and medical sciences
CD95 receptor expression
fas Receptor - analysis
Female
Humans
Immunohistochemistry
Kidney - chemistry
Kidney Neoplasms - chemistry
Kidney Neoplasms - pathology
Kidneys
Male
Medical sciences
Middle Aged
Neoplasm Staging
Nephrology. Urinary tract diseases
Prognosis
renal cell carcinoma
Survival Rate
Tumors of the urinary system
title Prognostic implications of CD95 receptor expression in clear cell renal carcinomas
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