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原发性胶质母细胞瘤培养物:干细胞标志物分析能否预测放射敏感性?

Primary glioblastoma cultures: can profiling of stem cell markers predict radiotherapy sensitivity?

作者信息

Lemke Dieter, Weiler Markus, Blaes Jonas, Wiestler Benedikt, Jestaedt Leonie, Klein Ann-Catherine, Löw Sarah, Eisele Günter, Radlwimmer Bernhard, Capper David, Schmieder Kirsten, Mittelbronn Michel, Combs Stephanie E, Bendszus Martin, Weller Michael, Platten Michael, Wick Wolfgang

机构信息

German Cancer Consortium (DKTK), Heidelberg, Germany.

Clinical Cooperation Unit Neurooncology, German Cancer Research Center (DKFZ), Heidelberg, Germany.

出版信息

J Neurochem. 2014 Oct;131(2):251-64. doi: 10.1111/jnc.12802. Epub 2014 Jul 18.

Abstract

Human glioblastomas may be hierarchically organized. Within this hierarchy, glioblastoma-initiating cells have been proposed to be more resistant to radiochemotherapy and responsible for recurrence. Here, established stem cell markers and stem cell attributed characteristics such as self-renewal capacity and tumorigenicity have been profiled in primary glioblastoma cultures to predict radiosensitivity. Furthermore, the sensitivity to radiotherapy of different subpopulations within a single primary glioblastoma culture was analyzed by a flow cytometric approach using Nestin, SRY (sex-determining region Y)-box 2 (SOX2) and glial fibrillary acidic protein. The protein expression of Nestin and SOX2 as well as the mRNA levels of Musashi1, L1 cell adhesion molecule, CD133, Nestin, and pleiomorphic adenoma gene-like 2 inversely correlated with radioresistance in regard to the clonogenic potential. Only CD44 protein expression correlated positively with radioresistance. In terms of proliferation, Nestin protein expression and Musashi1, pleiomorphic adenoma gene-like 2, and CD133 mRNA levels are inversely correlated with radioresistance. Higher expression of stem cell markers does not correlate with resistance to radiochemotherapy in the cancer genome atlas glioblastoma collective. SOX2 expressing subpopulations exist within single primary glioblastoma cultures. These subpopulations predominantly form the proliferative pool of the primary cultures and are sensitive to irradiation. Thus, profiling of established stem cell markers revealed a surprising result. Except CD44, the tested stem cell markers showed an inverse correlation between expression and radioresistance. Markers used to define glioma-initiating cells (GIC) are generally not defining a more resistant, but rather a more sensitive group of glioma cells. An exemption is CD44 expression. Also proliferation of the GIC culture itself was not systematically associated with radiosensitivity or - resistance, but a SOX-2 positive, proliferative subgroup within a GIC culture is showing the highest radiosensitivity.

摘要

人类胶质母细胞瘤可能具有分层结构。在这种分层结构中,有人提出胶质母细胞瘤起始细胞对放化疗更具抗性且是复发的原因。在此,已在原发性胶质母细胞瘤培养物中分析了既定的干细胞标志物以及诸如自我更新能力和致瘤性等干细胞属性特征,以预测放射敏感性。此外,通过使用巢蛋白、SRY(性别决定区Y)-盒2(SOX2)和胶质纤维酸性蛋白的流式细胞术方法,分析了单个原发性胶质母细胞瘤培养物中不同亚群对放疗的敏感性。就克隆形成潜力而言,巢蛋白和SOX2的蛋白表达以及Musashi1、L1细胞黏附分子、CD133、巢蛋白和多形性腺瘤样基因2的mRNA水平与放射抗性呈负相关。只有CD44蛋白表达与放射抗性呈正相关。在增殖方面,巢蛋白蛋白表达以及Musashi1、多形性腺瘤样基因2和CD133 mRNA水平与放射抗性呈负相关。在癌症基因组图谱胶质母细胞瘤群体中,干细胞标志物的高表达与放化疗抗性无关。单个原发性胶质母细胞瘤培养物中存在表达SOX2的亚群。这些亚群主要构成原发性培养物的增殖池,并且对辐射敏感。因此,对既定干细胞标志物的分析揭示了一个惊人的结果。除CD44外,所测试的干细胞标志物显示表达与放射抗性之间呈负相关。用于定义胶质瘤起始细胞(GIC)的标志物通常并未定义一组更具抗性的胶质瘤细胞,而是定义了一组更敏感的胶质瘤细胞。CD44表达是个例外。此外,GIC培养物本身的增殖与放射敏感性或抗性并无系统性关联,但GIC培养物中一个SOX-2阳性、增殖性亚群显示出最高的放射敏感性。

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