NONRANDOM CHROMOSOMAL GAINS IN PILOCYTIC ASTROCYTOMAS OF CHILDHOOD

被引:54
作者
WHITE, FV
ANTHONY, DC
YUNIS, EJ
TARBELL, NJ
SCOT, RM
SCHOFIELD, DE
机构
[1] CHILDRENS HOSP,DEPT PATHOL,BOSTON,MA 02115
[2] CHILDRENS HOSP,DEPT NEUROPATHOL,BOSTON,MA 02115
[3] CHILDRENS HOSP,DEPT RADIAT ONCOL,BOSTON,MA 02115
[4] CHILDRENS HOSP,DEPT NEUROL SURG,BOSTON,MA 02115
[5] HARVARD UNIV,SCH MED,JOINT CTR RADIAT THERAPY,BOSTON,MA 02115
[6] CHILDRENS HOSP PITTSBURGH,DEPT PATHOL,PITTSBURGH,PA 15213
关键词
ASTROCYTOMA; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION;
D O I
10.1016/0046-8177(95)90087-X
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Low-grade astrocytomas are the most common central nervous system (CNS) tumor occurring in the pediatric age group. Although many of these tumors are karyotypically normal, various studies have reported gains of chromosomes in a significant proportion of cases. We had the opportunity to karyotype two pilocytic astrocytomas occurring in 5- and 15-year-old children. These tumors were characterized by stemlines of 49,XY, +4, +7,+8 and 48,XX, +7, +8. Using these patients as index cases and based on additional karyotypic data that have been published, we performed fluorescence in situ hybridization on 25 additional cases of low-grade astrocytomas in children using pericentromeric probes for chromosomes 4, 6, 7, 8, 9, 10, 11, 12, 15, and 17. Six of 18 (excluding the two index cases), or one third, of the pilocytic astrocytomas were characterized by chromosomal gains, most commonly chromosomes 7 and 8, suggesting that trisomy 7 and 8 are relatively common events in the tumorigenesis of pilocytic astrocytomas. In contrast, chromosomal trisomies were not detected in seven well-differentiated fibrillary astrocytomas with any of the probes chosen. Copyright (C) 1995 by W.B. Saunders Company
引用
收藏
页码:979 / 986
页数:8
相关论文
共 41 条
[1]   INTERPHASE CYTOGENETICS REVEALS SOMATIC PAIRING OF CHROMOSOME-17 CENTROMERES IN NORMAL HUMAN BRAIN-TISSUE, BUT NO TRISOMY-7 OR SEX-CHROMOSOME LOSS [J].
ARNOLDUS, EPJ ;
NOORDERMEER, IA ;
PETERS, ACB ;
RAAP, AK ;
VANDERPLOEG, M .
CYTOGENETICS AND CELL GENETICS, 1991, 56 (3-4) :214-216
[2]   FEASIBILITY OF INSITU HYBRIDIZATION WITH CHROMOSOME SPECIFIC DNA PROBES ON PARAFFIN WAX EMBEDDED TISSUE [J].
ARNOLDUS, EPJ ;
DREEF, EJ ;
NOORDERMEER, IA ;
VERHEGGEN, MM ;
THIERRY, RF ;
PETERS, ACB ;
CORNELISSE, CJ ;
VANDERPLOEG, M ;
RAAP, AK .
JOURNAL OF CLINICAL PATHOLOGY, 1991, 44 (11) :900-904
[3]  
BELLO MJ, 1994, CANCER GENET CYTOGEN, V72, P55
[4]   MOLECULAR ANALYSIS OF GENOMIC ABNORMALITIES IN HUMAN GLIOMAS [J].
BELLO, MJ ;
DECAMPOS, JM ;
KUSAK, ME ;
VAQUERO, L ;
SARASA, JL ;
PESTANA, A ;
REY, JA .
CANCER GENETICS AND CYTOGENETICS, 1994, 73 (02) :122-129
[5]   CYTOGENETICS OF HUMAN BRAIN-TUMORS [J].
BIGNER, SH ;
MARK, J ;
BIGNER, DD .
CANCER GENETICS AND CYTOGENETICS, 1990, 47 (02) :141-154
[6]   MEDICAL PROGRESS - BRAIN-TUMORS .1. [J].
BLACK, PM .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (21) :1471-1476
[7]  
BURGER PC, 1991, SURGICAL PATHOLOGY N, P193
[8]  
CAVENEE WK, 1992, CANCER, V70, P1788, DOI 10.1002/1097-0142(19920915)70:4+<1788::AID-CNCR2820701621>3.0.CO
[9]  
2-L
[10]  
CHADDUCK WM, 1993, PEDIATR NEUROSURG, V17, P57