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星形细胞瘤患者中与发育及不良预后相关的基因改变研究。

Investigation of genetic alterations associated with development and adverse outcome in patients with astrocytic tumor.

作者信息

Cianciulli A M, Morace E, Coletta A M, Occhipinti E, Gandolfo G M, Leonardo G, Carapella C M

机构信息

Department of Clinical Pathology, Regina Elena Cancer Institute, Rome, Italy.

出版信息

J Neurooncol. 2000 Jun;48(2):95-101. doi: 10.1023/a:1006420921159.

DOI:10.1023/a:1006420921159
PMID:11083072
Abstract

Models describing progression in the genetic derangement of glial tumors have shown chromosomal loss and gain occurring most frequently in high-grade lesions, suggesting that identification of these aberrations may be prognostically significant. In this study, Fluorescence in situ hybridization (FISH) has been used to determine, and to confirm, loss and gain of chromosomes 1, 8, 10, 12 and 17, in formalin-fixed, paraffin-embedded brain biopsy tissue taken from 60 brain gliomas submitted to surgical resection or stereotactic biopsy. FISH analysis may be a valuable adjunct to histological grading. The results showed that this molecular cytogenetic technique is an important clinical and experimental tool that provides new insight on genetic alterations, confirming gain and loss of genetic material that occurs at the initiation and progression of human glioma. Our data suggests that potentially useful prognostic information may be obtained through this approach. Monosomy 10 was the most statistically significant negative predictor of patient survival, showing a significant correlation with the histological grading.

摘要

描述胶质细胞瘤基因紊乱进展的模型显示,染色体缺失和增加在高级别病变中最为常见,这表明识别这些畸变可能具有预后意义。在本研究中,荧光原位杂交(FISH)已被用于确定并确认取自60例接受手术切除或立体定向活检的脑胶质瘤的福尔马林固定、石蜡包埋脑活检组织中1、8、10、12和17号染色体的缺失和增加。FISH分析可能是组织学分级的一个有价值的辅助手段。结果表明,这种分子细胞遗传学技术是一种重要的临床和实验工具,它为基因改变提供了新的见解,证实了人类胶质瘤发生和进展过程中遗传物质的增加和缺失。我们的数据表明,通过这种方法可能获得潜在有用的预后信息。10号染色体单体是患者生存最具统计学意义的负性预测指标,与组织学分级显著相关。

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本文引用的文献

1
Acquisition of the glioblastoma phenotype during astrocytoma progression is associated with loss of heterozygosity on 10q25-qter.在星形细胞瘤进展过程中获得胶质母细胞瘤表型与10q25 - qter区域杂合性缺失相关。
Am J Pathol. 1999 Aug;155(2):387-94. doi: 10.1016/S0002-9440(10)65135-8.
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星形细胞瘤的比较基因组杂交分析:预后及诊断意义
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Fluorescence in situ hybridization (FISH) in diagnostic and investigative neuropathology.荧光原位杂交技术(FISH)在诊断性和研究性神经病理学中的应用
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通过间期细胞遗传学检测复发性星形细胞瘤和少突胶质细胞瘤活检组织中的染色体变化。
J Neuropathol Exp Neurol. 1997 Oct;56(10):1125-31. doi: 10.1097/00005072-199710000-00006.
4
Interphase cytogenetic (in situ hybridization) analysis of astrocytomas using archival, formalin-fixed, paraffin-embedded tissue and nonfluorescent light microscopy.利用存档的、福尔马林固定、石蜡包埋组织及非荧光光学显微镜对星形细胞瘤进行间期细胞遗传学(原位杂交)分析。
Am J Clin Pathol. 1997 Aug;108(2):166-74. doi: 10.1093/ajcp/108.2.166.
5
Molecular biology of malignant degeneration of astrocytoma.
Pediatr Neurosurg. 1996;24(1):41-9. doi: 10.1159/000121013.
6
Molecular pathways in the formation of gliomas.胶质瘤形成中的分子途径。
Glia. 1995 Nov;15(3):328-38. doi: 10.1002/glia.440150312.
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Loss of heterozygosity for loci on chromosome 10 is associated with morphologically malignant meningioma progression.10号染色体上基因座的杂合性缺失与形态学上恶性脑膜瘤的进展相关。
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Acta Cytol. 1993 May-Jun;37(3):391-6.
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Genetics of astrocytic tumor progression.
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