Corell Alba, Gómez Vecchio Tomás, Ferreyra Vega Sandra, Dénes Anna, Neimantaite Alice, Hagerius Alexander, Barchéus Hanna, Solheim Ole, Lindskog Cecilia, Bontell Thomas Olsson, Carén Helena, Jakola Asgeir S, Smits Anja
Department of Neurosurgery, Sahlgrenska University Hospital, Gothenburg, Sweden.
Department of Clinical Neuroscience, Institute of Neuroscience and Physiology, The Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Neurooncol Adv. 2022 Jun 4;4(1):vdac074. doi: 10.1093/noajnl/vdac074. eCollection 2022 Jan-Dec.
The subventricular zone (SVZ) of the human brain is a site of adult stem cell proliferation and a microenvironment for neural stem cells (NSCs). It has been suggested that NSCs in the SVZ are potential cells of origin containing driver mutations of glioblastoma, but their role in the origin of diffuse lower-grade gliomas (dLGGs) is not much studied.
We included 188 patients ≥18 years with -mutated dLGG (WHO grades 2-3) histologically diagnosed between 2007 and 2020. Tissue microarrays of tumor samples for patients between 2007 and 2016 were used for immunodetection of Nestin, SOX2, SOX9, KLF4, NANOG, CD133 cMYC, and Ki67. DNA methylation profile was used for stemness index (mDNAsi). Tumor contact with the SVZ was assessed and the distance was computed.
Overall, 70.2% of the dLGG had SVZ contact. Tumors with SVZ contact were larger (102.4 vs 30.9 mL, < .01), the patients were older (44.3 vs 40.4 years, = .04) and more often had symptoms related to increased intracranial pressure (31.8% vs 7.1%, < .01). The expression of SOX2, SOX9, Nestin, and Ki67 showed intersample variability, but no difference was found between tumors with or without SVZ contact, nor with the actual distance to the SVZ. mDNAsi was similar between groups ( = .42).
We found no statistical relationship between proximity with the SVZ and mDNAsi or expression of SOX2, SOX9, Nestin, and Ki67 in -mutated dLGG. Our data suggest that the potential impact of SVZ on -mutated dLGG is probably not associated with a more stemness-like tumor profile.
人类脑室下区(SVZ)是成体干细胞增殖的场所,也是神经干细胞(NSC)的微环境。有人提出,SVZ中的NSC是含有胶质母细胞瘤驱动突变的潜在起源细胞,但它们在弥漫性低级别胶质瘤(dLGG)起源中的作用研究较少。
我们纳入了188例年龄≥18岁、在2007年至2020年间经组织学诊断为-mutated dLGG(世界卫生组织2-3级)的患者。2007年至2016年间患者肿瘤样本的组织微阵列用于Nestin、SOX2、SOX9、KLF4、NANOG、CD133、cMYC和Ki67的免疫检测。DNA甲基化谱用于干性指数(mDNAsi)。评估肿瘤与SVZ的接触情况并计算距离。
总体而言,70.2%的dLGG与SVZ有接触。与SVZ有接触的肿瘤更大(102.4对30.9 mL,<0.01),患者年龄更大(44.3对40.4岁,=0.04),且更常出现与颅内压升高相关的症状(31.8%对7.1%,<0.01)。SOX2、SOX9、Nestin和Ki67的表达存在样本间差异,但在与SVZ有接触或无接触的肿瘤之间以及与到SVZ的实际距离之间均未发现差异。各组间mDNAsi相似(=0.42)。
我们发现,在-mutated dLGG中,与SVZ的接近程度与mDNAsi或SOX2、SOX9、Nestin和Ki67的表达之间不存在统计学关系。我们的数据表明,SVZ对-mutated dLGG的潜在影响可能与更具干细胞样的肿瘤特征无关。