Ki-67在脑膜瘤中的分布及其意义。

IF 3.6 2区 医学 Q1 CLINICAL NEUROLOGY
Xiaopeng Guo, Ruchit V Patel, James A Lederer, David M Meredith, Wenya Linda Bi
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引用次数: 0

摘要

目的:Ki-67是脑膜瘤中广泛使用的增殖标志物,影响预后评估和治疗决策,包括辅助放射治疗。然而,人们越来越认识到一些脑膜瘤富含免疫浸润,这可能会混淆Ki-67的解释,因为免疫细胞和肿瘤细胞都表现出增殖潜力。作者旨在剖析脑膜瘤微环境中Ki-67的细胞来源和分布,并探讨其临床、基因组和生物学相关性。方法:采用单细胞细胞计数技术(cytometry by time of flight [CyTOF])和单细胞RNA测序(scRNAseq)分析32例切除脑膜瘤的细胞组成,包括肿瘤和免疫谱系。免疫组织化学检测Ki-67指数和有丝分裂计数。评估CDKN2A/B缺失和高危染色体改变以建立分子综合等级。外推队列448新诊断脑膜瘤的总切除用于验证。结果:Ki-67在多种细胞系中表达,包括肿瘤细胞和免疫细胞,通过CyTOF在77,498个细胞上表达,scRNAseq在45,460个细胞上表达。促进Ki-67表达的细胞组成从WHO分级1级到2级和3级发生变化,WHO分级1级肿瘤中Ki-67+细胞主要由髓系细胞组成,而2级和3级脑膜瘤中非免疫肿瘤细胞以Ki-67+细胞为主。老年脑膜瘤患者的Ki-67指数明显升高,且受辐射照射时间的影响。与未来复发相关的最佳Ki-67阈值随随访时间而变化。此外,作者强调了两种局灶性Ki-67表达升高的情况,即中枢性梗死和髓外造血,其中明显的增殖与肿瘤侵袭性无关。结论:这些发现揭示了Ki-67在脑膜瘤中表达的复杂性,强调了对增殖指标进行细致解释的必要性。Ki-67指数仍然是评估脑膜瘤临床、分子和预后特征的可靠参数,需要仔细评估和考虑潜在的混杂因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ki-67 in meningioma: distribution and implications.

Objective: Ki-67 is a widely used marker of proliferation in meningiomas, influencing prognostic assessment and treatment decisions, including adjuvant radiation therapy. However, it is increasingly appreciated that some meningiomas are enriched with immune infiltration, which may confound Ki-67 interpretation as both immune and tumor cells exhibit proliferative potential. The authors aimed to dissect the cellular source and distribution of Ki-67 within the meningioma microenvironment and explore their clinical, genomic, and biological associations.

Methods: The cellular composition of 32 resected meningiomas, including tumor and immune lineages, was profiled with single-cell mass cytometry (cytometry by time of flight [CyTOF]) and single-cell RNA sequencing (scRNAseq). The Ki-67 index and mitotic count were assessed by immunohistochemistry. CDKN2A/B deletion and high-risk chromosome alterations were evaluated to establish a molecular Integrated Grade. An extrapolation cohort of 448 newly diagnosed meningiomas with gross-total resection was used for validation.

Results: Ki-67 is expressed by multiple cell lineages, both tumor and immune, as inferred by CyTOF on 77,498 cells and scRNAseq on 45,460 cells. The composition of cells contributing to Ki-67 expression changes from WHO grade 1 to grades 2 and 3, with Ki-67+ cells in WHO grade 1 tumors composed of mostly myeloid-lineage cells, while nonimmune tumor cells dominated Ki-67+ cells in grade 2 and 3 meningiomas. Ki-67 indices were markedly elevated in meningiomas from older patients (age > 70 years) and influenced by the timing of radiation exposure. The optimal Ki-67 threshold associated with future recurrence varied with time of follow-up. Furthermore, the authors highlight two scenarios of focally elevated Ki-67 expression, central infarction and extramedullary hematopoiesis, in which apparent proliferation does not correlate with tumor aggressiveness.

Conclusions: These findings unveil the complexity of Ki-67 expression in meningiomas, emphasizing the need for a nuanced interpretation of proliferation indices. The Ki-67 index remains a reliable parameter for assessing the clinical, molecular, and prognostic characteristics of meningiomas on careful evaluation and consideration of potential confounding factors.

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来源期刊
Journal of neurosurgery
Journal of neurosurgery 医学-临床神经学
CiteScore
7.20
自引率
7.30%
发文量
1003
审稿时长
1 months
期刊介绍: The Journal of Neurosurgery, Journal of Neurosurgery: Spine, Journal of Neurosurgery: Pediatrics, and Neurosurgical Focus are devoted to the publication of original works relating primarily to neurosurgery, including studies in clinical neurophysiology, organic neurology, ophthalmology, radiology, pathology, and molecular biology. The Editors and Editorial Boards encourage submission of clinical and laboratory studies. Other manuscripts accepted for review include technical notes on instruments or equipment that are innovative or useful to clinicians and researchers in the field of neuroscience; papers describing unusual cases; manuscripts on historical persons or events related to neurosurgery; and in Neurosurgical Focus, occasional reviews. Letters to the Editor commenting on articles recently published in the Journal of Neurosurgery, Journal of Neurosurgery: Spine, and Journal of Neurosurgery: Pediatrics are welcome.
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