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毛细胞型星形细胞瘤之间不同的基因特征与其脑区起源有关。

Distinct genetic signatures among pilocytic astrocytomas relate to their brain region origin.

作者信息

Sharma Mukesh K, Mansur David B, Reifenberger Guido, Perry Arie, Leonard Jeffrey R, Aldape Kenneth D, Albin Meredith G, Emnett Ryan J, Loeser Simon, Watson Mark A, Nagarajan Rakesh, Gutmann David H

机构信息

Department of Neurology, Washington University School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, USA.

出版信息

Cancer Res. 2007 Feb 1;67(3):890-900. doi: 10.1158/0008-5472.CAN-06-0973.

Abstract

Pilocytic astrocytomas (PAs) are the most common glioma in children. Whereas many PAs are slow-growing or clinically indolent, others exhibit more aggressive features with tumor recurrence and death. To identify genetic signatures that might predict PA clinical behavior, we did gene expression profiling on 41 primary PAs arising sporadically and in patients with neurofibromatosis type 1 (NF1). Whereas no expression signature was found that could discriminate clinically aggressive or recurrent tumors from more indolent cases, PAs arising in patients with NF1 did exhibit a unique gene expression pattern. In addition, we identified a gene expression signature that stratified PAs by location (supratentorial versus infratentorial). Lastly, we also identified a gene expression pattern common to PAs and normal mouse astrocytes and neural stem cells from these distinct brain regions as well as a gene expression pattern shared between PAs and another human glial tumor (ependymoma) arising supratentorially compared with those originating in the posterior fossa. These results suggest that glial tumors share an intrinsic, lineage-specific molecular signature that reflects the brain region in which their nonmalignant predecessors originated.

摘要

毛细胞型星形细胞瘤(PAs)是儿童中最常见的胶质瘤。虽然许多PA生长缓慢或临床上呈惰性,但其他一些则表现出更具侵袭性的特征,伴有肿瘤复发和死亡。为了确定可能预测PA临床行为的基因特征,我们对41例散发性和1型神经纤维瘤病(NF1)患者的原发性PA进行了基因表达谱分析。虽然未发现能够区分临床侵袭性或复发性肿瘤与更惰性病例的表达特征,但NF1患者中发生的PA确实表现出独特的基因表达模式。此外,我们确定了一种根据位置(幕上与幕下)对PA进行分层的基因表达特征。最后,我们还确定了PA与来自这些不同脑区的正常小鼠星形胶质细胞和神经干细胞共有的基因表达模式,以及与幕上发生的另一种人类胶质瘤(室管膜瘤)相比,PA与起源于后颅窝的胶质瘤之间共有的基因表达模式。这些结果表明,胶质瘤共享一种内在的、谱系特异性的分子特征,该特征反映了其非恶性前身起源的脑区。

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