EPIDERMAL GROWTH-FACTOR RECEPTOR EXPRESSION IN SQUAMOUS-CELL LUNG CARCINOMAS - AN IMMUNOHISTOCHEMICAL AND GENE ANALYSIS IN FORMALIN-FIXED, PARAFFIN-EMBEDDED MATERIAL

被引:21
作者
GORGOULIS, V
GIATROMANOLAKI, A
KARAMERIS, A
TSATSANIS, C
ANINOS, D
OZANNE, B
VESLEMES, M
JORDANOGLOU, J
TRIGIDOU, R
PAPASTAMATIOU, H
SPANDIDOS, DA
机构
[1] RED CROSS HOSP, DEPT PATHOL, ATHENS, GREECE
[2] NATL HELLEN RES FDN, GR-5011 ATHENS, GREECE
[3] ARMY GEN HOSP 401, DEPT PATHOL, ATHENS, GREECE
[4] BEATSON INST CANC RES, GLASGOW G61 1BD, SCOTLAND
[5] UNIV ATHENS, SOTIRIA HOSP, SCH MED, DEPT PULM, ATHENS, GREECE
[6] GEN HOSP ATHENS, DEPT CYTOL, ATHENS, GREECE
[7] SOTIRIA HOSP, DEPT PATHOL, ATHENS, GREECE
[8] UNIV CRETE, SCH MED, IRAKLION, GREECE
关键词
EPIDERMAL GROWTH FACTOR RECEPTOR; SQUAMOUS CELL LUNG CARCINOMA; SOUTHERN BLOT; DIFFERENTIAL POLYMERASE CHAIN REACTION; IMMUNOHISTOCHEMISTRY;
D O I
10.1007/BF01606894
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Epidermal growth factor (EGF) and its receptor (EGFr) constitute an important and well-characterized mitogenic system in various ectodermal tissues. We evaluated the expression of EGFr and examined possible EGFr gene alterations in 18 formalin-fixed, paraffin-embedded squamous cell lung carcinomas (SCLC) by an immunohistochemical assay, Southern blotting and differential polymerase chain reaction (DPCR). The immunohistochemical study employing the F4 and EGF-R1 monoclonal antibodies, directed against the intra- and extra-cellular portion of the receptor respectively, showed EGFr over-expression in 89% of the SCLC cases examined. All cases showed positive immunostaining for both antibodies, thus excluding the possibility of truncated receptors. In addition, analysis of the EGFr gene was carried out by Southern blotting and DPCR on paraffin extracted DNA from the same carcinoma cases. We found amplification of the EGFr gene in 5/18 (27%) SCLCs. All 5 positive cases showed EGFr over-expression, suggesting a possible correlation between the presence of EGFr gene amplification and over-expression of receptor protein. No correlation was observed among EGFr staining, EGFr gene amplification and differentiation of carcinomas. In addition, Southern blot analysis with HER-A2, a probe which hybridizes a sequence of the receptor's intracellular domain, revealed three novel EcoRI restriction fragment patterns. We suggest that these patterns correspond to EcoRI polymorphic sites of the receptor's tyrosine kinase domain.
引用
收藏
页码:295 / 302
页数:8
相关论文
共 31 条
[1]   EXPRESSION OF THE EPIDERMAL GROWTH-FACTOR RECEPTOR IN ASTROCYTIC TUMORS IS SPECIFICALLY ASSOCIATED WITH GLIOBLASTOMA-MULTIFORME [J].
AGOSTI, RM ;
LEUTHOLD, M ;
GULLICK, WJ ;
YASARGIL, MG ;
WIESTLER, OD .
VIRCHOWS ARCHIV A-PATHOLOGICAL ANATOMY AND HISTOPATHOLOGY, 1992, 420 (04) :321-325
[2]   EPIDERMAL GROWTH-FACTOR RECEPTORS IN LUNG-TUMORS [J].
BERGER, MS ;
GULLICK, WJ ;
GREENFIELD, C ;
EVANS, S ;
ADDIS, BJ ;
WATERFIELD, MD .
JOURNAL OF PATHOLOGY, 1987, 152 (04) :297-307
[3]   EVALUATION OF EPIDERMAL GROWTH-FACTOR RECEPTORS IN BLADDER-TUMORS [J].
BERGER, MS ;
GREENFIELD, C ;
GULLICK, WJ ;
HALEY, J ;
DOWNWARD, J ;
NEAL, DE ;
HARRIS, AL ;
WATERFIELD, MD .
BRITISH JOURNAL OF CANCER, 1987, 56 (05) :533-537
[4]   GENE AMPLIFICATION AND DRUG-RESISTANCE [J].
BROWN, R .
JOURNAL OF PATHOLOGY, 1991, 163 (04) :287-292
[5]   I125 LABELED HUMAN EPIDERMAL GROWTH-FACTOR - BINDING, INTERNALIZATION, AND DEGRADATION IN HUMAN FIBROBLASTS [J].
CARPENTER, G ;
COHEN, S .
JOURNAL OF CELL BIOLOGY, 1976, 71 (01) :159-171
[6]   EPIDERMAL GROWTH-FACTOR, ITS RECEPTOR, AND RELATED PROTEINS [J].
CARPENTER, G ;
ZENDEGUI, JG .
EXPERIMENTAL CELL RESEARCH, 1986, 164 (01) :1-10
[7]   EXPRESSION OF EPIDERMAL GROWTH-FACTOR RECEPTOR (EGF-R) IN HUMAN-LUNG TUMORS [J].
CERNY, T ;
BARNES, DM ;
HASLETON, P ;
BARBER, PV ;
HEALY, K ;
GULLICK, W ;
THATCHER, N .
BRITISH JOURNAL OF CANCER, 1986, 54 (02) :265-269
[8]  
DAMJANOV I, 1986, LAB INVEST, V55, P588
[9]   METABOLISM AND EFFECTS OF EPIDERMAL GROWTH-FACTOR AND RELATED GROWTH-FACTORS IN MAMMALS [J].
FISHER, DA ;
LAKSHMANAN, J .
ENDOCRINE REVIEWS, 1990, 11 (03) :418-442
[10]  
GORGOULIS V, 1992, ANTICANCER RES, V12, P1183