c-kit is not expressed in malignant mesothelioma

被引:20
作者
Horvai, AE
Li, L
Xu, ZD
Kramer, MJ
Jablons, DM
Treseler, PA
机构
[1] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Surg, San Francisco, CA 94143 USA
关键词
mesothelioma; c-kit; CD117; immunohistochemistry; STI571;
D O I
10.1097/01.MP.0000083647.69123.5C
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Overexpression of 1UT protein (CD 117), the product of the c-kit gene, has been shown to have important prognostic and therapeutic implications for a number of malignant neoplasms. Previous studies have shown conflicting results regarding the expression of c-kit in malignant mesothelioma. To determine whether malignant mesothelioma expresses KIT, immunohistochemistry and RT-PCR were used to analyze archived tissue from 37 cases of mesothelioma. Although a subset of mesotheliomas demonstrated specific staining with the DAKO anti-KIT antibody, in each case staining was nuclear. We could not detect c-kit mRNA by a sensitive RT-PCR assay, even in cases with strong nuclear staining. Furthermore, a second anti-Kit antibody (Cell-Marque) only demonstrated staining in a single mesothelioma case and in none of the cases that demonstrated nuclear staining. We conclude that immunoreactivity for KIT in mesothelioma does not represent expression of the c-kit gene and may represent antibody cross-reaction with nuclear proteins. Our results raise doubt about previously reported expression of KIT in mesothelioma and consequently, the applicability of therapeutic agents that target the kinase activity of KIT.
引用
收藏
页码:818 / 822
页数:5
相关论文
共 18 条
[1]   Paraffin section detection of the c-kit gene product (CD117) in human tissues:: Value in the diagnosis of mast cell disorders [J].
Arber, DA ;
Tamayo, R ;
Weiss, LM .
HUMAN PATHOLOGY, 1998, 29 (05) :498-504
[2]   Expression of stem-cell factor and its receptor c-kit protein in normal testicular tissue and malignant germ-cell tumours [J].
Bokemeyer, C ;
Kuczyk, MA ;
Dunn, T ;
Serth, J ;
Hartmann, K ;
Jonasson, J ;
Pietsch, T ;
Jonas, U ;
Schmoll, HJ .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1996, 122 (05) :301-306
[3]   Malignant pleural mesothelioma [J].
Boutin, C ;
Schlesser, M ;
Frenay, C ;
Astoul, P .
EUROPEAN RESPIRATORY JOURNAL, 1998, 12 (04) :972-981
[4]  
DEALAVA E, 2002, MODERN PATHOL, V15, pA301
[5]   Increased expression of epidermal growth factor receptor in rat pleural mesothelial cells correlates with carcinogenicity of mineral fibres [J].
Faux, SP ;
Houghton, CE ;
Hubbard, A ;
Patrick, G .
CARCINOGENESIS, 2000, 21 (12) :2275-2280
[6]   Inhibition of KIT tyrosine kinase activity: A novel molecular approach to the treatment of KIT-positive malignancies [J].
Heinrich, MC ;
Blanke, CD ;
Druker, BJ ;
Corless, CL .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (06) :1692-1703
[7]   Factors predictive of survival among 337 patients with mesothelioma treated between 1984 and 1994 by the Cancer and Leukemia Group B [J].
Herndon, JE ;
Green, MR ;
Chahinian, AP ;
Corson, JM ;
Suzuki, Y ;
Vogelzang, NJ .
CHEST, 1998, 113 (03) :723-731
[8]  
Huncharek M, 1996, ANTICANCER RES, V16, P1265
[9]   DIFFERENTIAL EXPRESSION OF THE C-KIT PROTOONCOGENE IN GERM-CELL TUMORS [J].
IZQUIERDO, MA ;
VANDERVALK, P ;
VANARKOTTE, J ;
RUBIO, G ;
GERMALLUCH, JR ;
UEDA, R ;
SCHEPER, RJ ;
TAKAHASHI, T ;
GIACCONE, G .
JOURNAL OF PATHOLOGY, 1995, 177 (03) :253-258
[10]   KIT extracellular and kinase domain mutations in gastrointestinal stromal tumors [J].
Lux, ML ;
Rubin, BP ;
Biase, TL ;
Chen, CJ ;
Maclure, T ;
Demetri, G ;
Xiao, S ;
Singer, S ;
Fletcher, CDM ;
Fletcher, JA .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 156 (03) :791-795