i3S- Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal; Cancer Drug Resistance Group, IPATIMUP - Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal; Department of Biological Sciences, FFUP - Faculty of Pharmacy of the University of Porto, Porto, Portugal.
i3S- Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal; Cancer Drug Resistance Group, IPATIMUP - Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal.
Drug Resist Updat. 2019 Dec;47:100647. doi: 10.1016/j.drup.2019.100647. Epub 2019 Oct 15.
Cancer-derived extracellular vesicles (EVs) have been detected in the bloodstream and other biofluids of cancer patients. They carry various tumor-derived molecules such as mutated DNA and RNA fragments, oncoproteins as well as miRNA and protein signatures associated with various phenotypes. The molecular cargo of EVs partially reflects the intracellular status of their cellular origin, however various sorting mechanisms lead to the enrichment or depletion of EVs in specific nucleic acids, proteins or lipids. It is becoming increasingly clear that cancer-derived EVs act in a paracrine and systemic manner to promote cancer progression by transferring aggressive phenotypic traits and drug-resistant phenotypes to other cancer cells, modulating the anti-tumor immune response, as well as contributing to remodeling the tumor microenvironment and formation of pre-metastatic niches. These findings have raised the idea that cancer-derived EVs may serve as analytes in liquid biopsies for real-time monitoring of tumor burden and drug resistance. In this review, we have summarized recent longitudinal clinical studies describing promising EV-associated biomarkers for cancer progression and tracking cancer evolution as well as pre-clinical and clinical evidence on the relevance of EVs for monitoring the emergence or progression of drug resistance. Furthermore, we outlined the state-of-the-art in the development and commercialization of EV-based biomarkers and discussed the scientific and technological challenges that need to be met in order to translate EV research into clinically applicable tools for precision medicine.
癌症来源的细胞外囊泡 (EVs) 已在癌症患者的血液和其他生物体液中被检测到。它们携带各种肿瘤来源的分子,如突变的 DNA 和 RNA 片段、癌蛋白以及与各种表型相关的 miRNA 和蛋白质特征。EVs 的分子货物部分反映了其细胞起源的细胞内状态,然而各种分选机制导致特定核酸、蛋白质或脂质中 EVs 的富集或耗尽。越来越明显的是,癌症来源的 EVs 通过将侵袭性表型特征和耐药表型转移到其他癌细胞、调节抗肿瘤免疫反应,以及有助于重塑肿瘤微环境和形成前转移龛,以旁分泌和全身性方式发挥作用,从而促进癌症进展。这些发现提出了这样一种观点,即癌症来源的 EVs 可以作为液体活检中的分析物,用于实时监测肿瘤负担和耐药性。在这篇综述中,我们总结了最近描述癌症进展和跟踪癌症演变的有前途的 EV 相关生物标志物的纵向临床研究,以及关于 EV 用于监测耐药性出现或进展的相关性的临床前和临床证据。此外,我们概述了基于 EV 的生物标志物的开发和商业化的最新进展,并讨论了为将 EV 研究转化为精准医学中临床适用的工具而需要解决的科学和技术挑战。