MAGE antigen expression in monophasic and biphasic synovial sarcoma

被引:16
作者
Antonescu, CR
Busam, KJ
Iversen, K
Kolb, D
Coplan, K
Spagnoli, GC
Ladanyi, M
Old, LJ
Jungbluth, AA
机构
[1] Mem Sloan Kettering Canc Ctr, Ludwig Inst Canc Res, New York Branch, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10021 USA
[3] Univ Basel, Dept Surg, Basel, Switzerland
[4] Univ Basel, Dept Res, Basel, Switzerland
关键词
synovial sarcoma; MAGE antigen expression;
D O I
10.1053/hupa.2002.31295
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Synovial sarcomas are high-grade malignant mesenchymal tumors carrying a pathognomonic cytogenetic alteration t(X;18) involving the SYT gene on chromosome IS and either SSX1 or SSX2 on chromosome X. Morphologically, biphasic (BSS) and monophasic (MSS) variants can be distinguished. Cancer/testis (CT) antigens are expressed in a variety of malignant tumors, but not in normal tissues except in germ cells, primarily of the testis. Anti-MACE monoclonal antibody (mAb) 57B previously showed a high incidence and homogenous reactivity pattern in a preliminary analysis of synovial sarcomas. This study was performed to analyze the expression of MACE by immunohistochemistry with mAb 57B in 25 synovial sarcomas (12 monophasic, 13 biphasic), which were typed for the t(X;18)-derived fusion transcript by reverse transcriptase polymerase chain reaction (19 SYT-SSX1, 6 SYT-SSX2). 57B immunoreactivity was present in 22 of 25 (88%) cases, and antigen expression was homogeneous in 14 of 22 57B-positive cases. Both morphological variants and both translocation types were immunoreactive; three SYT-SSX1 tumors (one MSS, two BSS) were 57B negative. Our study demonstrates that MAGE is frequently and homogeneously expressed in synovial sarcomas of both morphological variants and both translocation types, making these tumors an attractive target for MAGE antigen-based immunotherapy. Copyright 2002, Elsevier Science (USA). All rights reserved.
引用
收藏
页码:225 / 229
页数:5
相关论文
共 42 条
[1]   Strong association of SYT-SSX fusion type and morphologic epithelial differentiation in synovial sarcoma [J].
Antonescu, CR ;
Kawai, A ;
Leung, DH ;
Lonardo, F ;
Woodruff, JM ;
Healey, JH ;
Ladanyi, M .
DIAGNOSTIC MOLECULAR PATHOLOGY, 2000, 9 (01) :1-8
[2]   Alterations of cell cycle regulators in localized synovial sarcoma - A multifactorial study with prognostic implications [J].
Antonescu, CR ;
Leung, DH ;
Dudas, M ;
Ladanyi, M ;
Brennan, M ;
Woodruff, JM ;
Cordon-Cardo, C .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 156 (03) :977-983
[3]  
Argani P, 1998, MODERN PATHOL, V11, P65
[4]   BAGE - A NEW GENE ENCODING AN ANTIGEN RECOGNIZED ON HUMAN MELANOMAS BY CYTOLYTIC T-LYMPHOCYTES [J].
BOEL, P ;
WILDMANN, C ;
SENSI, ML ;
BRASSEUR, R ;
RENAULD, JC ;
COULIE, P ;
BOON, T ;
VANDERBRUGGEN, P .
IMMUNITY, 1995, 2 (02) :167-175
[5]   Tumor antigens [J].
Boon, T ;
Old, LJ .
CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (05) :681-683
[6]   The SYT protein involved in the t(X;18) synovial sarcoma translocation is a transcriptional activator localised in nuclear bodies [J].
Brett, D ;
Whitehouse, S ;
Antonson, P ;
Shipley, J ;
Cooper, C ;
Goodwin, G .
HUMAN MOLECULAR GENETICS, 1997, 6 (09) :1559-1564
[7]   Immunoreactivity with the anti-MAGE antibody 57B in malignant melanoma: Frequency of expression and correlation with prognostic parameters [J].
Busam, KJ ;
Iversen, K ;
Berwick, M ;
Spagnoli, GC ;
Old, LJ ;
Jungbluth, AA .
MODERN PATHOLOGY, 2000, 13 (04) :459-465
[8]  
Chambost H, 2000, BLOOD, V95, P3530
[9]   Identification of multiple cancer/testis antigens by allogeneic antibody screening of a melanoma cell line library [J].
Chen, YT ;
Güre, AO ;
Tsang, S ;
Stockert, E ;
Jäger, E ;
Knuth, A ;
Old, LJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (12) :6919-6923
[10]  
Cheville JC, 1999, MODERN PATHOL, V12, P974