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伽玛刀放射外科不会改变散发性前庭神经鞘瘤的拷贝数畸变谱。

Gamma Knife Radiosurgery does not alter the copy number aberration profile in sporadic vestibular schwannoma.

机构信息

Department of Clinical Science, University of Bergen, Bergen, Norway.

Center for Medical Genetics and Molecular Medicine, Haukeland University Hospital, Bergen, Norway.

出版信息

J Neurooncol. 2020 Sep;149(3):373-381. doi: 10.1007/s11060-020-03631-4. Epub 2020 Sep 27.

Abstract

INTRODUCTION

Ionizing radiation is a known etiologic factor in tumorigenesis and its role in inducing malignancy in the treatment of vestibular schwannoma has been debated. The purpose of this study was to identify a copy number aberration (CNA) profile or specific CNAs associated with radiation exposure which could either implicate an increased risk of malignancy or elucidate a mechanism of treatment resistance.

METHODS

55 sporadic VS, including 18 treated with Gamma Knife Radiosurgery (GKRS), were subjected to DNA whole-genome microarray and/or whole-exome sequencing. CNAs were called and statistical tests were performed to identify any association with radiation exposure. Hierarchical clustering was used to identify CNA profiles associated with radiation exposure.

RESULTS

A median of 7 (0-58) CNAs were identified across the 55 VS. Chromosome 22 aberration was the only recurrent event. A median aberrant cell fraction of 0.59 (0.25-0.94) was observed, indicating several genetic clones in VS. No CNA or CNA profile was associated with GKRS.

CONCLUSION

GKRS is not associated with an increase in CNAs or alteration of the CNA profile in VS, lending support to its low risk. This also implies that there is no major issue with GKRS treatment failure being due to CNAs. In agreement with previous studies, chromosome 22 aberration is the only recurrent CNA. VS consist of several genetic clones, addressing the need for further studies on the composition of cells in this tumor.

摘要

简介

电离辐射是肿瘤发生的已知病因,其在治疗前庭神经鞘瘤时诱导恶性肿瘤的作用一直存在争议。本研究的目的是确定与辐射暴露相关的拷贝数异常(CNA)谱或特定 CNA,这些 CNA 既可以暗示恶性肿瘤的风险增加,也可以阐明治疗耐药的机制。

方法

对 55 例散发性听神经瘤(VS)患者进行了 DNA 全基因组微阵列和/或全外显子组测序,其中包括 18 例接受伽玛刀放射外科治疗(GKRS)的患者。对 CNA 进行了调用,并进行了统计检验以确定与辐射暴露的任何关联。使用层次聚类来识别与辐射暴露相关的 CNA 谱。

结果

在 55 例 VS 中,确定了中位数为 7(0-58)个 CNA。22 号染色体异常是唯一的复发性事件。观察到中位数异常细胞分数为 0.59(0.25-0.94),表明 VS 中有多个遗传克隆。没有 CNA 或 CNA 谱与 GKRS 相关。

结论

GKRS 与 VS 中的 CNA 增加或 CNA 谱改变无关,这支持其低风险。这也意味着 GKRS 治疗失败不是由于 CNA 引起的,没有重大问题。与之前的研究一致,22 号染色体异常是唯一的复发性 CNA。VS 由多个遗传克隆组成,这需要进一步研究该肿瘤中细胞的组成。

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