检测恶性神经胶质瘤中端粒延长途径的改变,以改善分子诊断。
Detection of the alternative lengthening of telomeres pathway in malignant gliomas for improved molecular diagnosis.
机构信息
French National Institute for Health and Medical Research (INSERM), UMR1103, 63001, Clermont-Ferrand, France.
French National Center on Scientific Research (CNRS), UMR6293, 63001, Clermont-Ferrand, France.
出版信息
J Neurooncol. 2017 Nov;135(2):381-390. doi: 10.1007/s11060-017-2585-7. Epub 2017 Jul 28.
Human malignant gliomas exhibit acquisition of either one of two telomere maintenance mechanisms, resulting from either reactivation of telomerase expression or activation of an alternative lengthening of telomeres (ALT) mechanism. In the present study, we analyzed 63 human malignant gliomas for the presence of ALT-specific extrachromosomal circles of telomeric DNA (C-circles) and measured telomerase expression, telomeric DNA content (Telo/Alu method), and telomeric repeat-containing RNAs (TERRA) levels. We also assessed histomolecular markers routinely used in clinical practice. The presence of C-circles significantly correlated with IDH1/2 mutation, MGMT exon 1 methylation, low Ki-67 immunostaining, increased telomeric DNA content, absence of functional ATRX protein and level of HTERT gene expression. In multivariate analysis, we observed a trend to a correlation between elevated TERRA levels and increased survival. Interestingly, the C-circles assay allowed to detect ALT activation in glioblastomas exhibiting wild-type IDH1/2 and ATRX expression. These results suggest that, after the correlations uncovered here have been confirmed on larger numbers of tumors, telomeric markers might be useful in improving diagnosis. They also point out to the utility of using the specific, sensitive and quantitative C-circle and Telo/Alu assays that can work with as few as 30 ng of tumor DNA.
人类恶性神经胶质瘤表现出获得两种端粒维持机制之一,这是由于端粒酶表达的重新激活或端粒的替代性延长(ALT)机制的激活。在本研究中,我们分析了 63 个人类恶性神经胶质瘤,以检测 ALT 特异性端粒 DNA 的额外染色体环(C-环)的存在,并测量了端粒酶表达、端粒 DNA 含量(Telo/Alu 方法)和端粒重复 RNA(TERRA)水平。我们还评估了临床实践中常规使用的组织分子标志物。C-环的存在与 IDH1/2 突变、MGMT 外显子 1 甲基化、低 Ki-67 免疫染色、端粒 DNA 含量增加、功能性 ATRX 蛋白缺失和 HTERT 基因表达水平相关。在多变量分析中,我们观察到端粒重复 RNA 水平升高与生存率升高之间存在相关性的趋势。有趣的是,C-环检测法能够检测到 IDH1/2 和 ATRX 表达野生型的胶质母细胞瘤中 ALT 的激活。这些结果表明,在对更多数量的肿瘤进行了这里揭示的相关性的确认后,端粒标志物可能有助于改善诊断。它们还指出了使用 C-环和 Telo/Alu 检测法的特异性、敏感性和定量的实用性,这些检测法可以使用低至 30ng 的肿瘤 DNA。