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少突星形细胞瘤中10号染色体缺失与不良预后的相关性

Association of chromosome 10 losses and negative prognosis in oligoastrocytomas.

作者信息

Bissola Lorena, Eoli Marica, Pollo Bianca, Merciai Bianca Maria, Silvani Antonio, Salsano Ettore, Maccagnano Carmelo, Bruzzone Maria Grazia, Fuhrman Conti Anna Maria, Solero Carlo Lazzaro, Giombini Sergio, Broggi Giovanni, Boiardi Amerigo, Finocchiaro Gaetano

机构信息

Department of Experimental Neurology and Diagnostics, Istituto Nazionale Neurologico Besta, Via Celoria 11, 20133 Milan, Italy.

出版信息

Ann Neurol. 2002 Dec;52(6):842-5. doi: 10.1002/ana.10405.

Abstract

Oligoastrocytomas are mixed gliomas harboring different genetic alterations and with heterogeneous clinical evolution. We have looked for correlations between genetic losses and clinical evolution in 34 oligoastrocytomas. Loss of heterozygosity (LOH) with different microsatellite markers was studied on chromosomes 1p, 10q, 17p, and 19q. LOH on 1p was found in 44% of the tumors, on 10q in 24%, on 17p in 18%, and on 19q in 38%. LOH on 1p and 19q was combined in 29% of the patients. LOH on 1p was associated with significantly longer overall survival (p = 0.0092) and LOH on 10q with shorter overall survival (p = 0.0206). The observation that LOH on 10q predicts a short survival in oligoastrocytomas is novel and provides further evidence that genetic analysis may help to predict the clinical evolution of different gliomas, giving a more rationale basis to therapeutic options.

摘要

少突星形细胞瘤是具有不同基因改变且临床病程异质性的混合性胶质瘤。我们在34例少突星形细胞瘤中寻找基因缺失与临床病程之间的相关性。使用不同的微卫星标记研究了1号染色体短臂(1p)、10号染色体长臂(10q)、17号染色体短臂(17p)和19号染色体长臂(19q)上的杂合性缺失(LOH)情况。44%的肿瘤存在1p上的LOH,24%存在10q上的LOH,18%存在17p上的LOH,38%存在19q上的LOH。29%的患者同时存在1p和19q上的LOH。1p上的LOH与显著更长的总生存期相关(p = 0.0092),而10q上的LOH与较短的总生存期相关(p = 0.0206)。10q上的LOH可预测少突星形细胞瘤患者生存期较短这一观察结果是新发现,为基因分析有助于预测不同胶质瘤的临床病程提供了进一步证据,从而为治疗方案提供更合理的依据。

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