AMPLIFICATION AND EXPRESSION OF THE EPIDERMAL GROWTH-FACTOR RECEPTOR GENE DURING THE PROGRESSION OF NEUROEPITHELIAL TUMORS INVIVO

被引:1
作者
DIEDRICH, U
BARON, E
BEHNKE, J
ZOLL, B
机构
[1] UNIV GOTTINGEN,INST HUMAN GENET,W-3400 GOTTINGEN,GERMANY
[2] UNIV GOTTINGEN,NEUROCHIRURG KLIN,W-3400 GOTTINGEN,GERMANY
关键词
PROGRESSION OF NEUROEPITHELIAL TUMORS; EPIDERMAL GROWTH FACTOR RECEPTOR LOCUS; MUTATION; EXPRESSION;
D O I
10.1007/BF00856813
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The epidermal growth factor receptor (EGFR) gene is homologous to the oncogene c-erbB. The occurrence of amplification and rearrangements at the EGFR gene locus is associated with malignancy in neuroepithelial tumours. Sixteen neuroepithelial tumours from eight patients with recurrence of their neoplasms were analysed for changes at the EGFR gene locus and for expression of EGFR. Ten tumours from five patients lacked changes at the EGFR gene locus. Three of eight individuals showed EGFR gene amplifications in both tumours with a higher grade of amplification in the second tumour. In addition to amplification, a rearrangement was found in both tumours of the first patient. In the second case an amplification of chromosome-7-specific c-met sequences was found in the regrown tumour, suggesting that a polysomy 7 was at least partly responsible for the higher copy number of the EGFR sequences. In both tumours of the third patient with EGFR gene amplification different alleles were amplified. In contrast to the findings at the DNA level the EGFR expression, analysed by immunohistochemical techniques, showed a more heterogeneous pattern after tumour progression.
引用
收藏
页码:465 / 468
页数:4
相关论文
共 21 条
[1]   GENE AMPLIFICATION IN MALIGNANT HUMAN GLIOMAS - CLINICAL AND HISTOPATHOLOGIC ASPECTS [J].
BIGNER, SH ;
BURGER, PC ;
WONG, AJ ;
WERNER, MH ;
HAMILTON, SR ;
MUHLBAIER, LH ;
VOGELSTEIN, B ;
BIGNER, DD .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1988, 47 (03) :191-205
[2]   GENETIC-ANALYSIS OF EPIDERMAL GROWTH-FACTOR ACTION - ASSIGNMENT OF HUMAN EPIDERMAL GROWTH-FACTOR RECEPTOR GENE TO CHROMOSOME-7 [J].
DAVIES, RL ;
GROSSE, VA ;
KUCHERLAPATI, R ;
BOTHWELL, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (07) :4188-4192
[3]   THE HUMAN MET ONCOGENE IS RELATED TO THE TYROSINE KINASE ONCOGENES [J].
DEAN, M ;
PARK, M ;
LEBEAU, MM ;
ROBINS, TS ;
DIAZ, MO ;
ROWLEY, JD ;
BLAIR, DG ;
VANDEWOUDE, GF .
NATURE, 1985, 318 (6044) :385-388
[4]   RARE HA-RAS AND C-MOS ALLELES IN PATIENTS WITH INTRACRANIAL TUMORS [J].
DIEDRICH, U ;
ECKERMANN, O ;
SCHMIDTKE, J .
NEUROLOGY, 1988, 38 (04) :587-589
[5]   AMPLIFICATION OF THE C-ERBB ONCOGENE IS ASSOCIATED WITH MALIGNANCY IN PRIMARY TUMORS OF NEUROEPITHELIAL TISSUE [J].
DIEDRICH, U ;
SOJA, S ;
BEHNKE, J ;
ZOLL, B .
JOURNAL OF NEUROLOGY, 1991, 238 (04) :221-224
[6]  
DOWNWARD J, 1983, NATURE, V307, P605
[7]  
EKSTRAND AJ, 1991, CANCER RES, V51, P2164
[8]   DELETION-MUTANT EPIDERMAL GROWTH-FACTOR RECEPTOR IN HUMAN GLIOMAS - EFFECT OF TYPE-II MUTATION ON RECEPTOR FUNCTION [J].
HUMPHREY, PA ;
GANGAROSA, LM ;
WONG, AJ ;
ARCHER, GE ;
LUNDJOHANSEN, M ;
BJERKVIG, R ;
LAERUM, OD ;
FRIEDMAN, HS ;
BIGNER, DD .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 178 (03) :1413-1420
[9]  
JAMES CD, 1988, CANCER RES, V48, P5546
[10]  
JAMES CD, 1991, CANCER RES, V51, P1684