Division of Pediatric Hematology-Oncology, Department of Pediatrics, Faculty of Medicine, University of Debrecen, 98 Nagyerdei Krt, 4032 Debrecen, Hungary.
Int J Mol Sci. 2022 May 23;23(10):5838. doi: 10.3390/ijms23105838.
MicroRNAs (miRNAs) are evolutionarily conserved small non-coding RNAs, that are involved in the multistep process of carcinogenesis, contributing to all established hallmarks of cancer. In this review, implications of miRNAs in hematological malignancies and their clinical utilization fields are discussed. As components of the complex regulatory network of gene expression, influenced by the tissue microenvironment and epigenetic modifiers, miRNAs are "micromanagers" of all physiological processes including the regulation of hematopoiesis and metabolic pathways. Dysregulated miRNA expression levels contribute to both the initiation and progression of acute leukemias, the metabolic reprogramming of malignantly transformed hematopoietic precursors, and to the development of chemoresistance. Since they are highly stable and can be easily quantified in body fluids and tissue specimens, miRNAs are promising biomarkers for the early detection of hematological malignancies. Besides novel opportunities for differential diagnosis, miRNAs can contribute to advanced chemoresistance prediction and prognostic stratification of acute leukemias. Synthetic oligonucleotides and delivery vehicles aim the therapeutic modulation of miRNA expression levels. However, major challenges such as efficient delivery to specific locations, differences of miRNA expression patterns between pediatric and adult hematological malignancies, and potential side effects of miRNA-based therapies should be considered.
微小 RNA(miRNA)是进化上保守的小非编码 RNA,参与致癌的多步骤过程,有助于癌症的所有既定标志。在这篇综述中,讨论了 miRNA 在血液系统恶性肿瘤及其临床应用领域的意义。作为基因表达复杂调控网络的组成部分,miRNA 受组织微环境和表观遗传修饰物的影响,是包括造血和代谢途径调节在内的所有生理过程的“微观管理者”。miRNA 表达水平的失调既导致了急性白血病的起始和进展,也导致了恶性转化造血前体细胞的代谢重编程,以及化疗耐药性的发展。由于它们在体液和组织标本中高度稳定且易于定量,miRNA 是血液系统恶性肿瘤早期检测的有前途的生物标志物。除了为鉴别诊断提供新的机会外,miRNA 还可以帮助预测急性白血病的化疗耐药性和预后分层。合成寡核苷酸和输送载体旨在调节 miRNA 表达水平的治疗。然而,应考虑到一些主要挑战,如向特定部位的有效输送、儿科和成人血液系统恶性肿瘤之间 miRNA 表达模式的差异,以及 miRNA 治疗的潜在副作用。