Immunohistochemical expression of bcl-2 protein in squamous cell carcinoma and basaloid carcinoma of the esophagus

被引:29
作者
Koide, N
Koike, S
Adachi, W
Amano, J
Usuda, N
Nagata, T
机构
[1] Department of Surgery, Shinshu University, School of Medicine, Matsumoto 390
[2] Dept. of Anatomy and Cell Biology, Shinshu University, School of Medicine, Matsumoto 390
来源
SURGERY TODAY-THE JAPANESE JOURNAL OF SURGERY | 1997年 / 27卷 / 08期
关键词
bcl-2; protein; apoptosis; esophageal carcinoma; basaloid carcinoma;
D O I
10.1007/BF02384977
中图分类号
R61 [外科手术学];
学科分类号
摘要
In the present study, the expression of bcl-2 protein in esophageal squamous cell carcinoma (SCC) and basaloid carcinoma (BC) was immunohistochemically examined, and its relation to tumor progression and postoperative survival was determined in SCC, A total of 42 SCC and 4 BC tumor samples were fixed with formalin, embedded in paraffin, and stained using monoclonal bcl-2 protein antibody, clone 124, Immunoreactivity was semiquantitatively scored, and the staining results were compared with the pathologic features and survival rates, The cytoplasm of basal cells from the normal esophageal epithelium was stained, In some well- and moderately differentiated SCCs, bcl-2 protein-positive reaction was observed in the peripheral part of the tumor cord, but in poorly differentiated SCC, the cells were weakly or hardly stained, However, in BC, the cells were strongly stained, The immunoreactivity was positive in 45.2% of the SCCs and all of the BCs, There were no significant differences in pathological features or patient survival between the bcl-2 protein-positive and protein-negative SCCs, In conclusion, the expression was not related to tumor progression and had no prognostic significance in SCC. Conversely, BC had strong immunohistochemical expression, probably associated with the differentiation of carcinoma cells simulating the basal cells of the esophagus.
引用
收藏
页码:685 / 691
页数:7
相关论文
共 31 条
[1]   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
[2]  
CAMPOS L, 1993, BLOOD, V81, P3091
[3]  
CASTLE VP, 1993, AM J PATHOL, V143, P1543
[4]   ANTIGEN UNMASKING ON FORMALIN-FIXED, PARAFFIN-EMBEDDED TISSUE-SECTIONS [J].
CATTORETTI, G ;
PILERI, S ;
PARRAVICINI, C ;
BECKER, MHG ;
POGGI, S ;
BIFULCO, C ;
KEY, G ;
DAMATO, L ;
SABATTINI, E ;
FEUDALE, E ;
REYNOLDS, F ;
GERDES, J ;
RILKE, F .
JOURNAL OF PATHOLOGY, 1993, 171 (02) :83-98
[5]   THE BCL-2 CANDIDATE PROTO-ONCOGENE PRODUCT IS A 24-KILODALTON INTEGRAL-MEMBRANE PROTEIN HIGHLY EXPRESSED IN LYMPHOID-CELL LINES AND LYMPHOMAS CARRYING THE T(14,18) TRANSLOCATION [J].
CHENLEVY, Z ;
NOURSE, J ;
CLEARY, ML .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (02) :701-710
[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]  
COLOMBEL M, 1993, AM J PATHOL, V143, P390
[9]  
DOGLIONI C, 1994, VIRCHOWS ARCH, V424, P47
[10]   IDENTIFICATION OF PROGRAMMED CELL-DEATH INSITU VIA SPECIFIC LABELING OF NUCLEAR-DNA FRAGMENTATION [J].
GAVRIELI, Y ;
SHERMAN, Y ;
BENSASSON, SA .
JOURNAL OF CELL BIOLOGY, 1992, 119 (03) :493-501