Department of General Biology, Laboratory of Mutagenesis and Oncogenetics, Center of Biologic Sciences, State University of Londrina, Rodovia Celso Garcia Cid, PR-445, Km 380-University Campus, Londrina, PR, CEP 86057-970, Brazil.
Barretos Cancer Hospital (Molecular Oncology Research Center), Barretos, SP, CEP 14784-400, Brazil.
J Cancer Res Clin Oncol. 2022 Oct;148(10):2893-2910. doi: 10.1007/s00432-022-04213-9. Epub 2022 Aug 4.
Prostate cancer (PCa) is the 4th most diagnosed cancer and the 8th leading cause of cancer-related death worldwide. Currently, clinical risk stratification models including factors like PSA levels, Gleason score, and digital rectal examination are used for this purpose. There is a need for novel biomarkers that can distinguish between indolent and aggressive pathology and reduce the risk of overdiagnosis/overtreatment. Liquid biopsy has a non-invasive character, can lead to less morbidity and provide new biomarkers, such as miRNAs, that regulate diverse important cellular processes. Here, we report an extended revision about the role of cell-free and exosomal miRNAs (exomiRNAs) as biomarkers for screening, diagnosis, prognosis, or treatment of PCa.
A comprehensive review of the published literature was conducted focusing on the usefulness, advantages, and clinical applications of cell-free and exomiRNAs in serum and plasma. Using PubMed database 53 articles published between 2012 and 2021 were selected and discussed from the perspective of their use as diagnostic, prognostic and therapeutic biomarkers for PCa.
We identify 119 miRNAs associated with PCa development and the cell-free and exosomal miR-21, miR-141, miR-200c, and miR-375 were consistently associated with progression in multiple cohorts/studies. However, standardized experimental procedures, and well-defined and clinically relevant cohort studies are urgently needed to confirm the biomarker potential of cell-free and exomiRNAs in serum or plasma.
Cell-free and exomiRNAs in serum or plasma are promising tools for be used as non-invasive biomarkers for diagnostic, prognosis, therapy improvement and clinical outcome prediction in PCa patients.
前列腺癌(PCa)是全球第 4 大常见癌症,也是第 8 大癌症相关死亡原因。目前,临床风险分层模型包括 PSA 水平、Gleason 评分和直肠指检等因素用于此目的。需要新型生物标志物来区分惰性和侵袭性病理,并降低过度诊断/过度治疗的风险。液体活检具有非侵入性,可减少发病率,并提供新的生物标志物,如 miRNA,调节多种重要的细胞过程。在这里,我们报告了关于无细胞和外泌体 miRNA(exomiRNA)作为 PCa 筛查、诊断、预后或治疗的生物标志物的作用的扩展修订。
对已发表的文献进行了全面综述,重点关注无细胞和外泌体 miRNA 在血清和血浆中的有用性、优势和临床应用。使用 PubMed 数据库,选择了 2012 年至 2021 年间发表的 53 篇文章,并从其作为 PCa 诊断、预后和治疗生物标志物的角度进行了讨论。
我们确定了 119 个与 PCa 发展相关的 miRNA,无细胞和外泌体 miR-21、miR-141、miR-200c 和 miR-375 在多个队列/研究中与进展一致相关。然而,迫切需要标准化的实验程序和明确的、具有临床相关性的队列研究来确认无细胞和外泌体 miRNA 在血清或血浆中的生物标志物潜力。
血清或血浆中的无细胞和外泌体 miRNA 是一种很有前途的工具,可以作为非侵入性生物标志物,用于诊断、预后、改善治疗和预测 PCa 患者的临床结局。