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体外和体内循环肿瘤标志物在脑脊液诊断和治疗中的新前沿。

New Frontiers in Diagnosis and Therapy of Circulating Tumor Markers in Cerebrospinal Fluid In Vitro and In Vivo.

机构信息

Laboratory of Biomedical Photoacoustics, Saratov State University, 83 Astrakhanskaya St, 410012 Saratov, Russia.

Arkansas Nanomedicine Center & Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.

出版信息

Cells. 2019 Oct 2;8(10):1195. doi: 10.3390/cells8101195.

Abstract

One of the greatest challenges in neuro-oncology is diagnosis and therapy (theranostics) of leptomeningeal metastasis (LM), brain metastasis (BM) and brain tumors (BT), which are associated with poor prognosis in patients. Retrospective analyses suggest that cerebrospinal fluid (CSF) is one of the promising diagnostic targets because CSF passes through central nervous system, harvests tumor-related markers from brain tissue and, then, delivers them into peripheral parts of the human body where CSF can be sampled using minimally invasive and routine clinical procedure. However, limited sensitivity of the established clinical diagnostic cytology in vitro and MRI in vivo together with minimal therapeutic options do not provide patient care at early, potentially treatable, stages of LM, BM and BT. Novel technologies are in demand. This review outlines the advantages, limitations and clinical utility of emerging liquid biopsy in vitro and photoacoustic flow cytometry (PAFC) in vivo for assessment of CSF markers including circulating tumor cells (CTCs), circulating tumor DNA (ctDNA), microRNA (miRNA), proteins, exosomes and emboli. The integration of in vitro and in vivo methods, PAFC-guided theranostics of single CTCs and targeted drug delivery are discussed as future perspectives.

摘要

神经肿瘤学面临的最大挑战之一是脑脊髓液(CSF)中循环肿瘤细胞(CTC)、循环肿瘤 DNA(ctDNA)、微小 RNA(miRNA)、蛋白质、外泌体和栓子等标志物的检测,包括脑膜转移(LM)、脑转移(BM)和脑肿瘤(BT)的诊断和治疗(治疗诊断学)。这些转移与患者预后不良有关。回顾性分析表明,CSF 是一种很有前途的诊断靶点,因为 CSF 穿过中枢神经系统,从脑组织中采集与肿瘤相关的标志物,然后将其输送到人体的外周部位,在这些部位可以使用微创和常规的临床程序采集 CSF。然而,现有的临床诊断细胞学在体外的敏感性有限,MRI 在体内的敏感性有限,再加上治疗选择有限,无法为 LM、BM 和 BT 的早期、潜在可治疗阶段的患者提供治疗。因此,需要新的技术。本文综述了新兴的体外液体活检和体内光声流动细胞学(PAFC)在评估 CSF 标志物中的优势、局限性和临床应用,包括循环肿瘤细胞(CTC)、循环肿瘤 DNA(ctDNA)、微小 RNA(miRNA)、蛋白质、外泌体和栓子。讨论了体外和体内方法的整合、PAFC 指导的单个 CTC 治疗诊断学和靶向药物递送作为未来的展望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7af/6830088/14701c70dcc0/cells-08-01195-g001.jpg

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