Expression of the c-kit receptor in choroidal melanomas

被引:29
作者
Mouriaux, F
Kherrouche, Z
Maurage, CA
Demailly, FX
Labalette, P
Saule, S
机构
[1] Ctr Hosp Lens, Serv Ophtalmol, F-62307 Lens, France
[2] Salengro Hosp, Dept Neuropathol, F-59037 Lille, France
[3] Huriez Hosp, Dept Ophthalmol, F-59037 Lille, France
[4] Inst Curie, UMR 146, F-91405 Orsay, France
关键词
Choroidal; c-kit; melanoma; proliferation; protein;
D O I
10.1097/00008390-200304000-00008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The KIT gene encodes c-kit, a transmembrane receptor that has tyrosine kinase activity and plays a role in haematopoiesis, gametogenesis and melanogenesis. The c-kit protein is found in normal cutaneous and choroidal melanocytes, and there is evidence that expression is lost in melanoma. Expression of c-kit was analysed in 57 paraffin-embedded sections of choroidal melanoma specimens and three choroidal melanoma cell lines using immunochemistry and Western blotting. Of the tumour specimens, 75% stained positively for c-kit with a membrane pattern of reactivity. Of the six patients who underwent proton beam therapy before enucleation, five tumours exhibited no c-kit immunoreactivity and the other tumour demonstrated weak staining. Of the three melanoma cell lines used, c-kit expression was observed in only one. No correlations between c-kit positivity and parameters such as cell type, largest macroscopic tumour dimension, scleral invasion or pigmentation were observed. In contrast, a significant positive association was found between c-kit staining and mitotic activity (P= 0.02). However, c-kit expression did not significantly influence survival when evaluated by univariate analysis. In conclusion, c-kit is expressed in most choroidal melanoma tumours. Further analysis should provide new insights into the mechanisms underlying the molecular and cellular changes in choroidal melanomas.
引用
收藏
页码:161 / 166
页数:6
相关论文
共 36 条
[1]  
Albert DM, 1998, AM J OPHTHALMOL, V125, P745
[2]   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
[3]   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
[4]   Immunohistochemical expression of the c-kit proto-oncogene product in human malignant and non-malignant breast tissues [J].
Chui, X ;
Egami, H ;
Yamashita, J ;
Kurizaki, T ;
Ohmachi, H ;
Yamamoto, S ;
Ogawa, M .
BRITISH JOURNAL OF CANCER, 1996, 73 (10) :1233-1236
[5]   C-KIT-KINASE INDUCES A CASCADE OF PROTEIN TYROSINE PHOSPHORYLATION IN NORMAL HUMAN MELANOCYTES IN RESPONSE TO MAST-CELL GROWTH-FACTOR AND STIMULATES MITOGEN-ACTIVATED PROTEIN-KINASE BUT IS DOWN-REGULATED IN MELANOMAS [J].
FUNASAKA, Y ;
BOULTON, T ;
COBB, M ;
YARDEN, Y ;
FAN, BL ;
LYMAN, SD ;
WILLIAMS, DE ;
ANDERSON, DM ;
ZAKUT, R ;
MISHIMA, Y ;
HALABAN, R .
MOLECULAR BIOLOGY OF THE CELL, 1992, 3 (02) :197-209
[6]  
GERDES J, 1984, J IMMUNOL, V133, P1710
[7]   GROWTH-FACTORS, RECEPTOR KINASES, AND PROTEIN TYROSINE PHOSPHATASES IN NORMAL AND MALIGNANT MELANOCYTES [J].
HALABAN, R ;
FAN, BL ;
AHN, J ;
FUNASAKA, Y ;
GITAYGOREN, H ;
NEUFELD, G .
JOURNAL OF IMMUNOTHERAPY, 1992, 12 (03) :154-161
[8]  
Halaban R, 1991, Cancer Treat Res, V54, P19
[9]  
HIBI K, 1991, ONCOGENE, V6, P2291
[10]  
Hou L, 2000, DEVELOPMENT, V127, P5379