Sorolla Maria Alba, Sorolla Anabel, Parisi Eva, Salud Antonieta, Porcel José M
Research Group of Cancer Biomarkers, Biomedical Research Institute of Lleida (IRBLleida), 25198 Lleida, Spain.
Department of Medical Oncology, Arnau de Vilanova University Hospital (HUAV), 25198 Lleida, Spain.
Cancers (Basel). 2021 Jun 4;13(11):2798. doi: 10.3390/cancers13112798.
Liquid biopsy is emerging as a promising non-invasive diagnostic tool for malignant pleural effusions (MPE) due to the low sensitivity of conventional pleural fluid (PF) cytological examination and the difficulty to obtain tissue biopsies, which are invasive and require procedural skills. Currently, liquid biopsy is increasingly being used for the detection of driver mutations in circulating tumor DNA (ctDNA) from plasma specimens to guide therapeutic interventions. Notably, malignant PF are richer than plasma in tumor-derived products with potential clinical usefulness, such as ctDNA, micro RNAs (miRNAs) and long non-coding RNAs (lncRNAs), and circulating tumor cells (CTC). Tumor-educated cell types, such as platelets and macrophages, have also been added to this diagnostic armamentarium. Herein, we will present an overview of the role of the preceding biomarkers, collectively known as liquid biopsy, in PF samples, as well as the main technical approaches used for their detection and quantitation, including a proper sample processing. Technical limitations of current platforms and future perspectives in the field will also be addressed. Using PF as liquid biopsy shows promise for use in current practice to facilitate the diagnosis and management of metastatic MPE.
由于传统胸腔积液(PF)细胞学检查的敏感性较低,且获取组织活检存在困难(组织活检具有侵入性且需要操作技能),液体活检正逐渐成为一种有前景的用于恶性胸腔积液(MPE)的非侵入性诊断工具。目前,液体活检越来越多地用于检测血浆样本中循环肿瘤DNA(ctDNA)的驱动突变,以指导治疗干预。值得注意的是,恶性PF比血浆富含更多具有潜在临床用途的肿瘤衍生产物,如ctDNA、微小RNA(miRNA)、长链非编码RNA(lncRNA)和循环肿瘤细胞(CTC)。肿瘤驯化的细胞类型,如血小板和巨噬细胞,也已被纳入这一诊断手段。在此,我们将概述上述统称为液体活检的生物标志物在PF样本中的作用,以及用于其检测和定量的主要技术方法,包括适当的样本处理。还将讨论当前平台的技术局限性以及该领域的未来前景。将PF用作液体活检在当前实践中显示出有助于转移性MPE的诊断和管理的前景。