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脑胶质瘤瘤周区的组织病理学血管研究。

Histopathological vascular investigation of the peritumoral brain zone of glioblastomas.

机构信息

Department of Neurosurgery, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan.

Department of Pathology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan.

出版信息

J Neurooncol. 2018 Jan;136(2):233-241. doi: 10.1007/s11060-017-2648-9. Epub 2017 Nov 29.

Abstract

To date, no histopathological vascular investigation focusing on peritumoral brain zone (PBZ) has been reported for glioblastoma. We analyzed 10 newly diagnosed cases of glioblastomas. For these PBZs, histopathological investigation was performed by hematoxylin-eosin (H&E) staining and immunohistochemistry was analyzed for CD31, CD34, Factor VIII, VEGF, VEGFR-1/2, Ki67, p53 and nestin. Although it was difficult to identify PBZ by H&E, Ki67 and p53 staining, there were apparent differences in nestin staining among PBZ, tumor core (TC), and normal zone (NZ). Therefore, in this study, we divided PBZ from TC and NZ by nestin staining. Differences in histological features, microvessel density, expression of VEGF and its receptors were assessed for PBZ, TC and NZ. The microvessel density, as determined by counting CD31, CD34 and VEGF receptors, and VEGF-A expression were lower in PBZ than TC. The expression patterns for CD31, CD34 and VEGF receptors in vessels show dissociation in PBZ. In addition, the vascular characteristics of the PBZ may correlate with findings of radiographic imaging. We provide the first clinicopathological evidence that PBZ exhibits unique angiogenic characteristics. These in situ observations will help to elucidate the mechanisms of tumor recurrence.

摘要

迄今为止,尚无针对胶质母细胞瘤瘤周脑区(PBZ)的组织病理学血管研究报告。我们分析了 10 例新诊断的胶质母细胞瘤病例。对这些 PBZ 进行了苏木精-伊红(H&E)染色的组织病理学检查,并通过免疫组织化学分析了 CD31、CD34、因子 VIII、VEGF、VEGFR-1/2、Ki67、p53 和巢蛋白。尽管 H&E、Ki67 和 p53 染色难以识别 PBZ,但 PBZ、肿瘤核心(TC)和正常区(NZ)之间的巢蛋白染色存在明显差异。因此,在这项研究中,我们通过巢蛋白染色将 PBZ 与 TC 和 NZ 区分开来。评估了 PBZ、TC 和 NZ 的组织学特征、微血管密度、VEGF 及其受体的表达差异。通过计数 CD31、CD34 和 VEGF 受体以及 VEGF-A 表达,PBZ 的微血管密度低于 TC。在 PBZ 中,血管中 CD31、CD34 和 VEGF 受体的表达模式存在分离。此外,PBZ 的血管特征可能与影像学表现相关。我们提供了 PBZ 表现出独特的血管生成特征的首个临床病理证据。这些原位观察结果将有助于阐明肿瘤复发的机制。

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