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分子生物学研究对儿童脑肿瘤认识的影响。

Impact of molecular biology studies on the understanding of brain tumors in childhood.

机构信息

Division of Pediatric Hematology/Oncology, Department of Pediatrics and Adolescent Medicine, Mayo Clinic, Rochester, MN 55905, USA.

出版信息

Curr Oncol Rep. 2012 Apr;14(2):206-12. doi: 10.1007/s11912-012-0214-3.

DOI:10.1007/s11912-012-0214-3
PMID:22237928
Abstract

Pediatric brain tumors are the second most common form of childhood malignancy. Brain tumors are a very heterogenous group of tumors and the pathogenesis of many of these tumors is yet to be clearly elucidated. Current diagnostic tools include histopathology and immunohistochemistry, but classification based on these means has significant limitations. As our understanding of the molecular biology of individual tumors continues to increase it has led to the identification of reliable and increasingly available molecular biomarkers. Molecular techniques are likely to complement current standard means of investigation and help not only overcome diagnostic challenges but may also result in better disease classification and risk stratification, leading to more personalized therapeutic approaches.

摘要

小儿脑肿瘤是儿童期第二常见的恶性肿瘤。脑肿瘤是一组非常异质性的肿瘤,其中许多肿瘤的发病机制仍未阐明。目前的诊断工具包括组织病理学和免疫组织化学,但基于这些方法的分类有很大的局限性。随着我们对个体肿瘤分子生物学的理解不断加深,已经确定了可靠且越来越可用的分子生物标志物。分子技术可能会补充当前标准的研究手段,不仅有助于克服诊断挑战,而且还可能导致更好的疾病分类和风险分层,从而实现更具个性化的治疗方法。

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本文引用的文献

1
MGMT promoter gene methylation in pediatric glioblastoma: analysis using MS-MLPA.儿童胶质母细胞瘤中MGMT启动子基因甲基化:采用甲基化特异性多重连接探针扩增技术进行分析
Childs Nerv Syst. 2011 Nov;27(11):1877-83. doi: 10.1007/s00381-011-1525-7. Epub 2011 Jul 26.
2
Nonsense mutation and inactivation of SMARCA4 (BRG1) in an atypical teratoid/rhabdoid tumor showing retained SMARCB1 (INI1) expression.在具有保留的 SMARCB1(INI1)表达的非典型畸胎瘤/横纹肌样瘤中存在 SMARCA4(BRG1)的无意义突变和失活。
Am J Surg Pathol. 2011 Jun;35(6):933-5. doi: 10.1097/PAS.0b013e3182196a39.
3
Embryonal tumor with abundant neuropil and true rosettes (ETANTR) with a focal amplification at chromosome 19q13.42 locus: further evidence of two new instances in China.
美国儿童脑肿瘤发病率在上升吗?来自监测、流行病学和最终结果(SEER)数据库分析的显著发病率和生存率结果。
Childs Nerv Syst. 2014 Jan;30(1):147-54. doi: 10.1007/s00381-013-2307-1. Epub 2013 Oct 27.
4
The alternative lengthening of telomere phenotype is significantly associated with loss of ATRX expression in high-grade pediatric and adult astrocytomas: a multi-institutional study of 214 astrocytomas.端粒延长的替代性表型与高级别儿童和成人星形细胞瘤中 ATRX 表达缺失显著相关:214 例星形细胞瘤的多机构研究。
Mod Pathol. 2013 Nov;26(11):1425-32. doi: 10.1038/modpathol.2013.90. Epub 2013 Jun 14.
具有丰富神经丛和真性菊形团的胚胎性肿瘤(ETANTR),在染色体 19q13.42 位置存在局灶性扩增:中国的两个新病例证据。
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