AMPLIFICATION OF EPIDERMAL GROWTH-FACTOR RECEPTOR GENE IN GLIOMAS - HISTOPATHOLOGY AND PROGNOSIS

被引:163
作者
HURTT, MR
MOOSSY, J
DONOVANPELUSO, M
LOCKER, J
机构
[1] UNIV PITTSBURGH,SCH MED,DEPT NEUROL,PITTSBURGH,PA 15261
[2] UNIV PITTSBURGH,SCH MED,DIV NEUROPATHOL,PITTSBURGH,PA 15261
[3] UNIV PITTSBURGH,SCH MED,PITTSBURGH CANC INST,PITTSBURGH,PA 15261
关键词
ANEUPLOIDY; CHROMOSOME-7; GENE AMPLIFICATION; GLIOMAS; MET; POLYSOMY; PROGNOSIS;
D O I
10.1097/00005072-199201000-00010
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In order to evaluate the incidence and prognostic significance of gene amplification in primary brain neoplasms we measured the number of gene copies per cell of three oncogenes (epidermal growth factor receptor [EGFR] gene, N-myc, C-myc) and syntenic control genes in 40 specimens using quantitative DNA dot blots. We observed EGFR gene amplification in astrocytomas and anaplastic astrocytomas with approximately the same incidence as in glioblastoma multiforme (33%), although large amplifications were only seen in glioblastoma multiforme. Fourteen patients had a supratentorial glioblastoma multiforme; six had EGFR gene amplification and eight had either normal EGFR gene copy number or elevated EGFR copy number attributable to extra copies of chromosome 7. Patients with gene amplification had shorter survival than patients without gene amplification (p = 0.0 1). The observed difference in survival was not likely to be due to group differences in age, sex, treatment, or histopathology.
引用
收藏
页码:84 / 90
页数:7
相关论文
共 32 条
[1]   HOMOGENEOUSLY STAINING CHROMOSOMAL REGIONS CONTAIN AMPLIFIED COPIES OF AN ABUNDANTLY EXPRESSED CELLULAR ONCOGENE (C-MYC) IN MALIGNANT NEUROENDOCRINE CELLS FROM A HUMAN-COLON CARCINOMA [J].
ALITALO, K ;
SCHWAB, M ;
LIN, CC ;
VARMUS, HE ;
BISHOP, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (06) :1707-1711
[2]   THE HUMAN THYROGLOBULIN GENE - A POLYMORPHIC MARKER LOCALIZED DISTAL TO C-MYC ON CHROMOSOME-8 BAND-Q24 [J].
BAAS, F ;
BIKKER, H ;
VANKESSEL, AG ;
MELSERT, R ;
PEARSON, PL ;
DEVIJLDER, JJM ;
VANOMMEN, GJB .
HUMAN GENETICS, 1985, 69 (02) :138-143
[3]   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
[4]  
BIGNER SH, 1988, CANCER RES, V48, P405
[5]   RELATIONSHIP BETWEEN GENE AMPLIFICATION AND CHROMOSOMAL DEVIATIONS IN MALIGNANT HUMAN GLIOMAS [J].
BIGNER, SH ;
WONG, AJ ;
MARK, J ;
MUHLBAIER, LH ;
KINZLER, KW ;
VOGELSTEIN, B ;
BIGNER, DD .
CANCER GENETICS AND CYTOGENETICS, 1987, 29 (01) :165-170
[6]   PATTERNS OF THE EARLY, GROSS CHROMOSOMAL CHANGES IN MALIGNANT HUMAN GLIOMAS [J].
BIGNER, SH ;
MARK, J ;
MAHALEY, MS ;
BIGNER, DD .
HEREDITAS, 1984, 101 (01) :103-113
[7]   CHROMOSOMAL EVOLUTION IN MALIGNANT HUMAN GLIOMAS STARTS WITH SPECIFIC AND USUALLY NUMERICAL DEVIATIONS [J].
BIGNER, SH ;
MARK, J ;
BULLARD, DE ;
MAHALEY, MS ;
BIGNER, DD .
CANCER GENETICS AND CYTOGENETICS, 1986, 22 (02) :121-135
[8]  
BURGER PC, 1980, CANCER, V46, P1179, DOI 10.1002/1097-0142(19800901)46:5<1179::AID-CNCR2820460517>3.0.CO
[9]  
2-0
[10]  
BURGER PC, 1985, CANCER, V56, P1106, DOI 10.1002/1097-0142(19850901)56:5<1106::AID-CNCR2820560525>3.0.CO