Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, 6 Tiantanxili, Beijing, China.
Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.
J Neurooncol. 2018 Jul;138(3):659-666. doi: 10.1007/s11060-018-2837-1. Epub 2018 Mar 19.
The newly proposed putamen classification system shows good prognostic value in patients with insular LGGs, yet no study towards the molecular profiles of putamen involved LGGs has been proposed.
Clinical information and imaging data of patients diagnosed with insular low-grade gliomas were collected retrospectively. Genetic information of the 34 tumors was assessed using RNA-sequencing. Gene set enrichment analysis was further performed to identify the genes showing differential expression between putamen-involved tumors and putamen non-involved tumors. The level of Ki-67 expression was also evaluated.
There were 843 genes identified to be differentially expressed between putamen-involved and non-involved gliomas. Specifically, Gene set enrichment analysis discovered 13 Kyoto Encyclopedia of Genes and Genomes pathways and 37 Gene Ontology Biological Process term were upregulated in putamen-involved low-grade glioma cells. The enriched GO sets with the highest gene counts included cell cycle (42 genes), mitotic cell cycle (24 genes), and cell division (19 genes). Furthermore, high expression of Ki-67 was associated with putamen involvement in insular gliomas.
There is clear genetic variation between putamen-involved and non-involved insular low-grade gliomas. The differential expression of genes related to the processes of cell proliferation, cell migration, or DNA repair may lead to putamen involvement. The findings suggest that among the two subtypes, putamen-involved insular low-grade gliomas have higher malignancy, and the clinical treatment towards the putamen-involved insular low-grade gliomas should be more active.
新提出的壳核分类系统在岛叶低级别胶质瘤患者中显示出良好的预后价值,但尚未提出针对壳核受累的低级别胶质瘤分子特征的研究。
回顾性收集诊断为岛叶低级别胶质瘤患者的临床信息和影像学资料。使用 RNA 测序评估 34 个肿瘤的遗传信息。进一步进行基因集富集分析,以确定在壳核受累肿瘤和壳核未受累肿瘤之间显示差异表达的基因。还评估了 Ki-67 表达水平。
确定了 843 个在壳核受累和未受累胶质瘤之间差异表达的基因。具体来说,基因集富集分析发现 13 个京都基因与基因组百科全书通路和 37 个基因本体生物学过程术语在壳核受累低级别胶质瘤细胞中上调。基因数量最高的富集 GO 集包括细胞周期(42 个基因)、有丝分裂细胞周期(24 个基因)和细胞分裂(19 个基因)。此外,Ki-67 高表达与岛叶胶质瘤壳核受累有关。
壳核受累和未受累岛叶低级别胶质瘤之间存在明显的遗传变异。与细胞增殖、细胞迁移或 DNA 修复过程相关的基因的差异表达可能导致壳核受累。研究结果表明,在这两种亚型中,壳核受累的岛叶低级别胶质瘤恶性程度更高,壳核受累的岛叶低级别胶质瘤的临床治疗应更加积极。