A hitchhiker's guide to cerebrospinal fluid biomarkers for neuro-oncology.

IF 16.4 1区 医学 Q1 CLINICAL NEUROLOGY
Cecile Riviere-Cazaux, Michael B Keough, Jeffrey A Zuccato, Rahul Kumar, Sebastian Schulz, Arthur E Warrington, Michael W Ruff, Benjamin M Ellingson, Nader Sanai, Jian L Campian, Sani H Kizilbash, Ian F Parney, Gelareh Zadeh, Mustafa Khasraw, Tobias Kessler, Ugur Sener, Daniel P Cahill, Alireza Mansouri, Terry C Burns
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引用次数: 0

Abstract

Cerebrospinal fluid (CSF) has emerged as a valuable liquid biopsy source for glioma biomarker discovery and validation. CSF produced within the ventricles circulates through the subarachnoid space, where the composition of glioma-derived analytes is influenced by the proximity and anatomical location of sampling relative to tumor, in addition to underlying tumor biology. The substantial gradients observed between lumbar and intracranial CSF compartments for tumor-derived analytes underscore the importance of sampling site selection. Moreover, radiographic features, such as tumor-CSF contact and blood-brain barrier disruption, are critical covariates that may affect biomarker detection and the abundance of plasma-derived analytes in CSF, respectively. Longitudinal intracranial CSF sampling, enabled by access devices like Ommaya reservoirs, may offer a window into treatment response and disease progression, though variability in analyte yield, sample volumes, and the dynamic effects of surgical resection pose challenges. This review critically evaluates the anatomic, radiographic, and longitudinal factors, or "time-space continuum," that impact glioma CSF biomarker abundance. Practical considerations for longitudinal CSF biobanking, including access device placement and collection, are also reviewed. Key takeaways and recommendations for CSF glioma biomarker discovery and validation are provided as a "hitchhiker's guide" based on our collective experience, along with resources for investigators aiming to develop CSF biobanking at their institutions.

神经肿瘤学CSF生物标志物的搭便车指南。
脑脊液(CSF)已成为胶质瘤生物标志物发现和验证的有价值的液体活检来源。脑室内产生的脑脊液通过蛛网膜下腔循环,除了潜在的肿瘤生物学外,胶质瘤衍生分析物的成分还受到采样相对于肿瘤的接近性和解剖位置的影响。在腰椎和颅内脑脊液室之间观察到的肿瘤来源分析物的大量梯度强调了采样地点选择的重要性。此外,放射学特征,如肿瘤-脑脊液接触和血脑屏障(BBB)破坏,是可能分别影响生物标志物可检测性和脑脊液中血浆来源分析物丰度的关键协变量。纵向颅内脑脊液取样,通过接入设备如Ommaya储液器,可以提供一个窗口,以了解治疗反应和疾病进展,尽管分析物产量、样本量和手术切除的动态影响的可变性带来了挑战。这篇综述批判性地评估了影响胶质瘤脑脊液生物标志物丰度的解剖学、影像学和纵向因素。纵向脑脊液生物库的实际考虑,包括访问装置的放置和收集,也进行了审查。根据我们的集体经验,提供了脑脊液胶质瘤生物标志物发现和验证的关键要点和建议,以及旨在在其机构开发脑脊液生物库的研究人员的资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neuro-oncology
Neuro-oncology 医学-临床神经学
CiteScore
27.20
自引率
6.30%
发文量
1434
审稿时长
3-8 weeks
期刊介绍: Neuro-Oncology, the official journal of the Society for Neuro-Oncology, has been published monthly since January 2010. Affiliated with the Japan Society for Neuro-Oncology and the European Association of Neuro-Oncology, it is a global leader in the field. The journal is committed to swiftly disseminating high-quality information across all areas of neuro-oncology. It features peer-reviewed articles, reviews, symposia on various topics, abstracts from annual meetings, and updates from neuro-oncology societies worldwide.
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