Overexpression of bcl-2 protein in synovial sarcoma: A comparative study of other soft tissue spindle cell sarcomas and an additional analysis by fluorescence fn situ hybridization

被引:74
作者
Hirakawa, N [1 ]
Naka, T [1 ]
Yamamoto, I [1 ]
Fukuda, T [1 ]
Tsuneyoshi, M [1 ]
机构
[1] KYUSHU UNIV, FAC MED, SCH HLTH & SCI, DEPT PATHOL 2, FUKUOKA, JAPAN
关键词
bcl-2; soft tissue sarcomas; synovial sarcoma; immunohistochemistry; paraffin-embedded tissue; fluorescence in situ hybridization; cytogenetic abnormality;
D O I
10.1016/S0046-8177(96)90284-1
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The expression of bcl-2 protein was analyzed in 19 synovial sarcomas and 29 additional soft tissue spindle cell sarcomas as controls by the immunohistologic staining of paraffin-embedded specimens; 15 of 19 (79%) synovial sarcoma cases were positive, but all other spindle cell sarcomas were negative including 20 leiomyosarcomas, 4 malignant peripheral nerve sheath tumors, and 4 fibrosarcomas. In 4 cases of bcl-2-positive synovial sarcoma (3 biphasic and 1 focally glandular type), bcl-2 protein staining was much stronger in the spindle cells than in the epithelial cells, A fluorescence in situ hybridization (FISH) analysis with centromeric and whole chromosome painting probes for chromosome 18 and X was performed on 7 synovial sarcomas, The six cases of bcl-2-positive synovial sarcoma consisted of live cases with the t(X; 18) and one case with tetrasomy of chromosome 18 and X. It has been speculated that bcl-2 protein expression is caused by the 14;18 translocation and other abnormalities of chromosome 18. This study thus showed the feasibility of such a correlation between bcl-2 protein expression and the characteristic cytogenetic abnormality in the synovial sarcoma-X;18 translocation. In addition, bcl-2 protein also appears to be a characteristic marker of synovial sarcoma and is thus considered to be potentially useful in distinguishing synovial sarcoma from other spindle cell sarcomas. Copyright (C) 1996 by W.B. Saunders Company.
引用
收藏
页码:1060 / 1065
页数:6
相关论文
共 39 条
[1]  
AISENBERG AC, 1988, BLOOD, V71, P969
[2]   CLONING THE CHROMOSOMAL BREAKPOINT OF T(14-18) HUMAN LYMPHOMAS - CLUSTERING AROUND JH ON CHROMOSOME-14 AND NEAR A TRANSCRIPTIONAL UNIT ON 18 [J].
BAKHSHI, A ;
JENSEN, JP ;
GOLDMAN, P ;
WRIGHT, JJ ;
MCBRIDE, OW ;
EPSTEIN, AL ;
KORSMEYER, SJ .
CELL, 1985, 41 (03) :899-906
[3]  
BRIDGE JA, 1988, CANCER, V62, P935, DOI 10.1002/1097-0142(19880901)62:5<935::AID-CNCR2820620514>3.0.CO
[4]  
2-E
[5]   TRANSLOCATION T(X-18) IN SYNOVIAL SARCOMA - ALUI ENDONUCLEASE DIGESTION FOR BREAKPOINT DETECTION IN 2 CASES [J].
CALABRESE, G ;
PALKA, G ;
DIVIRGILIO, C ;
CIANCHETTI, E ;
CARACINO, A ;
STUPPIA, L ;
ANGELUCCI, D .
CANCER GENETICS AND CYTOGENETICS, 1990, 50 (02) :277-279
[6]   CLONING AND STRUCTURAL-ANALYSIS OF CDNAS FOR BCL-2 AND A HYBRID BCL-2/IMMUNOGLOBULIN TRANSCRIPT RESULTING FROM THE T(14-18) TRANSLOCATION [J].
CLEARY, ML ;
SMITH, SD ;
SKLAR, J .
CELL, 1986, 47 (01) :19-28
[8]  
DALCIN P, 1992, MODERN PATHOL, V5, P357
[9]  
ELO J, 1993, EUR ARCH OTO-RHINO-L, V249, P499
[10]   DIAGNOSTIC RELEVANCE OF CLONAL CYTOGENETIC ABERRATIONS IN MALIGNANT SOFT-TISSUE TUMORS [J].
FLETCHER, JA ;
KOZAKEWICH, HP ;
HOFFER, FA ;
LAGE, JM ;
WEIDNER, N ;
TEPPER, R ;
PINKUS, GS ;
MORTON, CC ;
CORSON, JM .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (07) :436-442