Paraffin section detection of the c-kit gene product (CD117) in human tissues:: Value in the diagnosis of mast cell disorders

被引:239
作者
Arber, DA [1 ]
Tamayo, R [1 ]
Weiss, LM [1 ]
机构
[1] City Hope Natl Med Ctr, Div Pathol, Duarte, CA 91010 USA
关键词
c-kit; CD117; immunohistochemistry; mast cells; mast cell disease;
D O I
10.1016/S0046-8177(98)90066-1
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The c-hit gene product (CD117) is known to be expressed by a variety of normal human tissue cell types, including breast epithelium, germ cells, melanocytes, immature myeloid cells, and mast cells. To further characterize the expression of this antigen, 117 normal human tissues and 576 human tumors were studied by paraffin section immunohistochemistry. Varying degrees of CD117 expression were identified in various normal cells and in 53% of all tumors studied. In most cases (42% of total), CD117 expression was weak. Expression was most common in mast cell disease (100%), testicular germ cell tumors (100%), endometrial carcinomas (100%), papillary and follicular thyroid carcinomas (100%), small cell carcinomas (91%), malignant melanomas (90%), and ovarian epithelial carcinomas (87%). Strong immunoreactivity was only identified in cases of mast cell disease (11 of 11 cases), serous ovarian carcinoma (3 of 16), malignant melanoma (2 of 40), small cell lung carcinoma (one of seven), and adenoid cystic carcinoma (one of one). Although the pattern of reactivity was primarily cytoplasmic, a membrane staining pattern was seen in a subset of cases, and strong membrane staining was identified in normal mast cells and all cases of mast cell disease. The lack of tumor specificity of weak expression of this antigen limits its diagnostic utility in most cases. However, the strong membrane reactivity for CD117 identified in mast cells may be useful in the diagnosis of mast cell disorders. Copyright (C) 1998 by W.B. Saunders Company.
引用
收藏
页码:498 / 504
页数:7
相关论文
共 33 条
[1]   MOLECULAR-CLONING OF MAST-CELL GROWTH-FACTOR, A HEMATOPOIETIN THAT IS ACTIVE IN BOTH MEMBRANE-BOUND AND SOLUBLE FORMS [J].
ANDERSON, DM ;
LYMAN, SD ;
BAIRD, A ;
WIGNALL, JM ;
EISENMAN, J ;
RAUCH, C ;
MARCH, CJ ;
BOSWELL, HS ;
GIMPEL, SD ;
COSMAN, D ;
WILLIAMS, DE .
CELL, 1990, 63 (01) :235-243
[2]  
[Anonymous], ADV PATHOL LAB MED
[3]  
Arber DA, 1996, AM J CLIN PATHOL, V106, P462
[4]  
BATTIFORA H, 1990, LAB INVEST, V63, P722
[5]   A NEW ACUTE TRANSFORMING FELINE RETROVIRUS AND RELATIONSHIP OF ITS ONCOGENE V-KIT WITH THE PROTEIN-KINASE GENE FAMILY [J].
BESMER, P ;
MURPHY, JE ;
GEORGE, PC ;
QIU, F ;
BERGOLD, PJ ;
LEDERMAN, L ;
SNYDER, HW ;
BRODEUR, D ;
ZUCKERMAN, EE ;
HARDY, WD .
NATURE, 1986, 320 (6061) :415-421
[6]  
DEVRIES C, 1992, SCIENCE, V255, P898
[7]   EXPRESSION OF THE C-KIT GENE-PRODUCT IN NORMAL AND NEOPLASTIC MAST-CELLS BUT NOT IN NEOPLASTIC BASOPHIL/MAST CELL PRECURSORS FROM CHRONIC MYELOGENOUS LEUKEMIA [J].
FUKUDA, T ;
KAMISHIMA, T ;
TSUURA, Y ;
SUZUKI, T ;
KAKIHARA, T ;
NAITO, M ;
KISHI, I ;
MATSUMOTO, K ;
SHIBATA, A ;
SEITO, T .
JOURNAL OF PATHOLOGY, 1995, 177 (02) :139-146
[8]  
HIBI K, 1991, ONCOGENE, V6, P2291
[9]  
HINES SJ, 1995, CELL GROWTH DIFFER, V6, P769
[10]   THE HEMATOPOIETIC GROWTH FACTOR-KL IS ENCODED BY THE SI-LOCUS AND IS THE LIGAND OF THE C-KIT RECEPTOR, THE GENE-PRODUCT OF THE W-LOCUS [J].
HUANG, E ;
NOCKA, K ;
BEIER, DR ;
CHU, TY ;
BUCK, J ;
LAHM, HW ;
WELLNER, D ;
LEDER, P ;
BESMER, P .
CELL, 1990, 63 (01) :225-233