• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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。

Interphase cytogenetic (in situ hybridization) analysis of astrocytomas using archival, formalin-fixed, paraffin-embedded tissue and nonfluorescent light microscopy.

作者信息

Perry A, Tonk V, McIntire D D, White C L

机构信息

Department of Pathology, The University of Texas Southwestern Medical School, Dallas 75235-9072, USA.

出版信息

Am J Clin Pathol. 1997 Aug;108(2):166-74. doi: 10.1093/ajcp/108.2.166.

DOI:10.1093/ajcp/108.2.166
PMID:9260757
Abstract

Astrocytomas contain nonrandom chromosomal abnormalities that recently have been correlated with shortened patient survival. Two frequently reported aberrations are trisomy 7 and monosomy 10. We assessed the numerical complement of chromosomes 7 and 10 in formalin-fixed, paraffin-embedded brain biopsy tissue from 28 diffuse astrocytomas by in situ hybridization using a nonfluorescent enzymatic detection system. Clinical follow-up of at least 5 years was available in 26 cases (93%). Monosomy 10 was identified in 7 cases (25%): astrocytoma, 1 case; anaplastic astrocytoma, 1 case; and glioblastoma, 5 cases. Trisomy 7 was identified in 11 cases (39%): astrocytoma, 5 cases; glioblastoma, 6 cases. Multivariate analysis revealed that monosomy 10 was the most statistically significant negative predictor of patient survival. Numerical chromosomal abnormalities are detectable in astrocytomas in archival tissue using interphase cytogenetics and nonfluorescent light microscopy. Although larger studies are required, our data suggest that potentially useful prognostic information may be obtained with this approach.

摘要

星形细胞瘤存在非随机的染色体异常,最近的研究表明这些异常与患者生存期缩短相关。两种常见的畸变是7号染色体三体和10号染色体单体。我们使用非荧光酶检测系统,通过原位杂交技术评估了28例弥漫性星形细胞瘤的福尔马林固定、石蜡包埋脑活检组织中7号和10号染色体的数目。26例(93%)患者有至少5年的临床随访资料。10号染色体单体在7例(25%)中被检测到:星形细胞瘤1例;间变性星形细胞瘤1例;胶质母细胞瘤5例。7号染色体三体在11例(39%)中被检测到:星形细胞瘤5例;胶质母细胞瘤6例。多因素分析显示,10号染色体单体是患者生存期最具统计学意义的负性预测指标。使用间期细胞遗传学和非荧光光学显微镜可在存档组织的星形细胞瘤中检测到染色体数目异常。尽管需要更大规模的研究,但我们的数据表明,通过这种方法可能获得有用的预后信息。

相似文献

1
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.
2
Detection of chromosomal changes by interphase cytogenetics in biopsies of recurrent astrocytomas and oligodendrogliomas.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.
3
Utility of EGFR and PTEN numerical aberrations in the evaluation of diffusely infiltrating astrocytomas. Laboratory investigation.表皮生长因子受体(EGFR)和第10号染色体缺失的磷酸酶和张力蛋白同源物(PTEN)数值畸变在弥漫性浸润性星形细胞瘤评估中的效用。实验室研究。
J Neurosurg. 2008 Feb;108(2):330-5. doi: 10.3171/JNS/2008/108/2/0330.
4
Gain of chromosome 7, as detected by in situ hybridization, strongly correlates with shorter survival in astrocytoma grade 2.通过原位杂交检测发现,7号染色体增加与2级星形细胞瘤患者较短的生存期密切相关。
Genes Chromosomes Cancer. 2002 Mar;33(3):279-84. doi: 10.1002/gcc.10029.
5
Investigation of genetic alterations associated with development and adverse outcome in patients with astrocytic tumor.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。
J Neurooncol. 2000 Jun;48(2):95-101. doi: 10.1023/a:1006420921159.
6
Numerical aberrations of chromosomes 1, 2, and 7 in astrocytomas studied by interphase cytogenetics.
Genes Chromosomes Cancer. 1997 May;19(1):6-13. doi: 10.1002/(sici)1098-2264(199705)19:1<6::aid-gcc2>3.0.co;2-3.
7
Association of chromosome 7, chromosome 10 and EGFR gene amplification in glioblastoma multiforme.多形性胶质母细胞瘤中7号染色体、10号染色体与表皮生长因子受体基因扩增的关联
Clin Neuropathol. 2005 Sep-Oct;24(5):209-18.
8
Cytogenetic analysis of gliomas by in situ hybridization of stereotactic biopsy material.
Acta Neurochir (Wien). 1997;139(1):22-5. doi: 10.1007/BF01850863.
9
DNA in situ hybridization (interphase cytogenetics) versus comparative genomic hybridization (CGH) in human cancer: detection of numerical and structural chromosome aberrations.人类癌症中DNA原位杂交(间期细胞遗传学)与比较基因组杂交(CGH):检测染色体数目和结构畸变
Acta Histochem. 2000 Feb;102(1):85-94. doi: 10.1078/0065-1281-00540.
10
Age-related nonrandom chromosomal abnormalities in human low-grade astrocytomas.人类低级星形细胞瘤中与年龄相关的非随机染色体异常。
Hum Genet. 1993 Jul;91(6):547-50. doi: 10.1007/BF00205078.

引用本文的文献

1
Analysis of chromosome 7 in adult and pediatric ependymomas using chromogenic in situ hybridization.
J Neurooncol. 2005 Mar;72(1):25-8. doi: 10.1007/s11060-004-3117-9.
2
Analysis of 1p, 19q, 9p, and 10q as prognostic markers for high-grade astrocytomas using fluorescence in situ hybridization on tissue microarrays from Radiation Therapy Oncology Group trials.利用放射治疗肿瘤学组试验的组织微阵列,通过荧光原位杂交分析1p、19q、9p和10q作为高级别星形细胞瘤的预后标志物。
Neuro Oncol. 2004 Apr;6(2):96-103. doi: 10.1215/s1152851703000231.
3
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
Brain Pathol. 2002 Jan;12(1):67-86. doi: 10.1111/j.1750-3639.2002.tb00424.x.
4
Investigation of genetic alterations associated with development and adverse outcome in patients with astrocytic tumor.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。
J Neurooncol. 2000 Jun;48(2):95-101. doi: 10.1023/a:1006420921159.