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An astroblastoma case associated with loss of heterozygosity on chromosome 9p.

作者信息

Hata Nobuhiro, Shono Tadahisa, Yoshimoto Koji, Mizoguchi Masahiro, Kawamura Tadao, Nagata Shinji, Matsumoto Kenichi, Hayashi Kenshi, Iwaki Toru, Sasaki Tomio

机构信息

Department of Neurosurgery, Graduate School of Medical Science, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

出版信息

J Neurooncol. 2006 Oct;80(1):69-73. doi: 10.1007/s11060-006-9157-6. Epub 2006 Apr 25.

DOI:10.1007/s11060-006-9157-6
PMID:16636749
Abstract

The tumorigenesis of astroblastomas has not yet been elucidated on the basis of histopathological studies, and genetic studies may be useful for obtaining additional information regarding the tumorigenesis of these tumors. Here, we report an astroblastoma case in which a genetic analysis was performed. A 16-year-old female with a progressive headache was found to have a demarcated cystic tumor with a mural nodule in the right parietal lobe. Total removal of the tumor was achieved and a histological examination verified that the tumor was an astroblastoma. A genetic analysis using microsatellite markers revealed loss of heterozygosity (LOH) on chromosome 9p. The postoperative course was uneventful and, to date, she has been followed up for 2 years with no signs of recurrence. This is the first reported case of an astroblastoma in which LOH was detected on 9p. Based on this result, the tumorigenesis of astroblastomas is discussed.

摘要

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本文引用的文献

1
Comparative genomic hybridization in glioma: a meta-analysis of 509 cases.胶质瘤中的比较基因组杂交:509例病例的荟萃分析。
Cancer Genet Cytogenet. 2002 Jun;135(2):147-59. doi: 10.1016/s0165-4608(01)00650-1.
2
Correlation between localization, age, and chromosomal imbalances in ependymal tumours as detected by CGH.
J Pathol. 2002 Jun;197(2):238-44. doi: 10.1002/path.1086.
3
Multiplexed analysis of post-PCR fluorescence-labeled microsatellite alleles and statistical evaluation of their imbalance in brain tumors.脑肿瘤中PCR后荧光标记微卫星等位基因的多重分析及其失衡的统计学评估。
具有 MN1:BEND2 融合的高度复发性小儿高级神经上皮肿瘤的十年进化轨迹。
Sci Rep. 2018 Jan 18;8(1):1032. doi: 10.1038/s41598-018-19389-9.
4
Patterns of care and survival outcomes in patients with astroblastoma: an individual patient data analysis of 152 cases.成星形细胞瘤患者的治疗模式与生存结局:152例患者的个体患者数据分析
Childs Nerv Syst. 2017 Aug;33(8):1295-1302. doi: 10.1007/s00381-017-3410-5. Epub 2017 May 5.
5
Neuroradiologic characteristics of astroblastoma and systematic review of the literature: 2 new cases and 125 cases reported in 59 publications.成星形细胞瘤的神经放射学特征及文献系统综述:2例新病例及59篇出版物中报道的125例病例
Pediatr Radiol. 2016 Aug;46(9):1301-8. doi: 10.1007/s00247-016-3607-x. Epub 2016 Apr 5.
Jpn J Cancer Res. 2002 Mar;93(3):284-90. doi: 10.1111/j.1349-7006.2002.tb02170.x.
4
CDKN2A/p16 in ependymomas.室管膜瘤中的CDKN2A/p16
J Neurooncol. 2001 Aug;54(1):9-13. doi: 10.1023/a:1012537105775.
5
A study of loss of heterozygosity at 70 loci in anaplastic astrocytoma and glioblastoma multiforme with implications for tumor evolution.一项关于间变性星形细胞瘤和多形性胶质母细胞瘤中70个基因座杂合性缺失的研究及其对肿瘤演变的意义。
Neuro Oncol. 1999 Jul;1(3):169-76. doi: 10.1093/neuonc/1.3.169.
6
Identification of novel regions of allelic loss in ependymomas by high-resolution allelotyping with 384 microsatellite markers.通过使用384个微卫星标记进行高分辨率等位基因分型鉴定室管膜瘤中新型等位基因缺失区域。
J Neurosurg. 2001 Jul;95(1):9-14. doi: 10.3171/jns.2001.95.1.0009.
7
Astroblastoma: report of a case with microsatellite analysis.
Neuropathology. 2000 Sep;20(3):228-32. doi: 10.1046/j.1440-1789.2000.00335.x.
8
Astroblastoma: clinicopathologic features and chromosomal abnormalities defined by comparative genomic hybridization.成星形细胞瘤:通过比较基因组杂交确定的临床病理特征和染色体异常
Brain Pathol. 2000 Jul;10(3):342-52. doi: 10.1111/j.1750-3639.2000.tb00266.x.
9
The Ink4a tumor suppressor gene product, p19Arf, interacts with MDM2 and neutralizes MDM2's inhibition of p53.Ink4a肿瘤抑制基因产物p19Arf与MDM2相互作用,并中和MDM2对p53的抑制作用。
Cell. 1998 Mar 20;92(6):713-23. doi: 10.1016/s0092-8674(00)81400-2.
10
Role of the INK4a locus in tumor suppression and cell mortality.INK4a基因座在肿瘤抑制和细胞死亡中的作用。
Cell. 1996 Apr 5;85(1):27-37. doi: 10.1016/s0092-8674(00)81079-x.