Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Acta Neuropathol. 2011 Apr;121(4):529-43. doi: 10.1007/s00401-010-0773-z. Epub 2010 Nov 16.
Array comparative genomic hybridization (aCGH) is a powerful tool for detecting DNA copy number alterations (CNA). Because diffuse malignant gliomas are often sampled by small biopsies, formalin-fixed paraffin-embedded (FFPE) blocks are often the only tissue available for genetic analysis; FFPE tissues are also needed to study the intratumoral heterogeneity that characterizes these neoplasms. In this paper, we present a combination of evaluations and technical advances that provide strong support for the ready use of oligonucleotide aCGH on FFPE diffuse gliomas. We first compared aCGH using bacterial artificial chromosome (BAC) arrays in 45 paired frozen and FFPE gliomas, and demonstrate a high concordance rate between FFPE and frozen DNA in an individual clone-level analysis of sensitivity and specificity, assuring that under certain array conditions, frozen and FFPE DNA can perform nearly identically. However, because oligonucleotide arrays offer advantages to BAC arrays in genomic coverage and practical availability, we next developed a method of labeling DNA from FFPE tissue that allows efficient hybridization to oligonucleotide arrays. To demonstrate utility in FFPE tissues, we applied this approach to biphasic anaplastic oligoastrocytomas and demonstrate CNA differences between DNA obtained from the two components. Therefore, BAC and oligonucleotide aCGH can be sensitive and specific tools for detecting CNAs in FFPE DNA, and novel labeling techniques enable the routine use of oligonucleotide arrays for FFPE DNA. In combination, these advances should facilitate genome-wide analysis of rare, small and/or histologically heterogeneous gliomas from FFPE tissues.
阵列比较基因组杂交 (aCGH) 是检测 DNA 拷贝数改变 (CNA) 的有力工具。由于弥漫性恶性神经胶质瘤通常通过小活检采样,因此福尔马林固定石蜡包埋 (FFPE) 块通常是唯一可用于遗传分析的组织;还需要 FFPE 组织来研究这些肿瘤的特征性肿瘤内异质性。在本文中,我们提出了一系列评估和技术进步,为在 FFPE 弥漫性神经胶质瘤上使用寡核苷酸 aCGH 提供了有力支持。我们首先在 45 对冷冻和 FFPE 神经胶质瘤中比较了使用细菌人工染色体 (BAC) 阵列的 aCGH,并在个体克隆水平的敏感性和特异性分析中证明了 FFPE 和冷冻 DNA 之间的高一致性,确保在某些阵列条件下,冷冻和 FFPE DNA 的性能几乎相同。然而,由于寡核苷酸阵列在基因组覆盖范围和实际可用性方面优于 BAC 阵列,我们接下来开发了一种从 FFPE 组织中标记 DNA 的方法,该方法允许其与寡核苷酸阵列高效杂交。为了证明在 FFPE 组织中的实用性,我们将这种方法应用于双相性间变性少突胶质细胞瘤,并证明了从两个成分中获得的 DNA 之间的 CNA 差异。因此,BAC 和寡核苷酸 aCGH 可以成为检测 FFPE DNA 中 CNA 的敏感和特异性工具,并且新型标记技术使寡核苷酸阵列能够常规用于 FFPE DNA。综上所述,这些进展应该有助于从 FFPE 组织中对罕见、小和/或组织学上异质性的神经胶质瘤进行全基因组分析。