剖析胶质母细胞瘤的分子特征:探索脑室下区邻近性的影响。

Hidayet Safak Cine, Ece Uysal, Mehmet Emre Gunaydin, Eren Soguk
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引用次数: 0

摘要

目的:研究特定多形性胶质母细胞瘤(GBM)分子标记物与其脑室下区(SVZ)邻近性之间的相关性,以发现潜在的预后指标和治疗策略:研究回顾性分析了2016年至2022年期间接受脑室上区GBM手术的171例患者。GBM被分为SVZ接触组(SVZ + GBM)和SVZ非接触组(SVZ-GBM)。我们分析了IDH1、P53、ATRX、Ki67、GFAP和Olig2等分子标记物:结果:SVZ + GBM肿瘤(12.2 cm3)比SVZ-GBM肿瘤(4.8 cm3; p 0.001)更大。此外,100%的SVZ-GBM肿瘤中IDH1突变为阴性;ATRX缺失在SVZ + GBM肿瘤中的发生率(34.3%)高于SVZ-GBM肿瘤(4.5%;P 0.001)。SVZ 接触与 p53 值之间没有相关性(p = 0.134)。此外,Ki67 增殖指数和 Olig2 阳性与 SVZ 接触之间也没有差异(分别为 p = 0.306 和 p = 0.071)。然而,IDH1突变与SVZ接触存在相关性,所有IDH1阳性肿瘤均显示SVZ接触(p = 0.009):本研究揭示了GBM的SVZ接触与特定分子标记物(尤其是IDH1突变、ATRX缺失和肿瘤大小)之间的相关性。SVZ接触可作为GBM的分类标准,从而有助于提高对该疾病的认识和潜在的治疗干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Outlining the Molecular Profile of Glioblastoma: Exploring the Influence of Subventricular Zone Proximity.

Aim: To investigate the correlation between specific glioblastoma multiforme (GBM) molecular markers and their proximity to the subventricular zone (SVZ) to uncover potential prognostic indicators and therapeutic strategies.

Material and methods: The study retrospectively analyzed 171 patients who underwent surgery for supratentorial GBM from 2016 to 2022. GBMs were categorized into SVZ contact (SVZ + GBM) and SVZ noncontact (SVZ-GBM) groups. We analyzed molecular markers, such as IDH1, P53, ATRX, Ki67, GFAP, and Olig2.

Results: SVZ + GBM tumors were larger (12.2 cm3) than SVZ-GBM tumors (4.8 cm3; p < 0.001). Additionally, IDH1 mutation was negative in 100% of SVZ-GBM tumors; ATRX loss was more prevalent in SVZ + GBM tumors (34.3%) than in SVZ-GBM tumors (4.5%; p < 0.001). There was no correlation between SVZ contact and the p53 value (p=0.134). Furthermore, no difference was observed in the association of the Ki67 proliferation index and Olig2 positivity with SVZ contact (p=0.306, p=0.071, respectively). However, there was a correlation between IDH1 mutation and SVZ contact, with all IDH1-positive tumors showing SVZ contact (p=0.009).

Conclusion: This study revealed a correlation between SVZ contact in GBM and specific molecular markers, specifically IDH1 mutation, ATRX loss, and tumor size. SVZ contact could serve as criterion for categorizing GBMs, thus contributing to an improved understanding of the disease and potential therapeutic interventions.

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