Liccardo Francesca, Iaiza Alessia, Śniegocka Martyna, Masciarelli Silvia, Fazi Francesco
Department of Anatomical, Histological, Forensic & Orthopedic Sciences, Section of Histology & Medical Embryology, Sapienza University of Rome, Via A. Scarpa, 14-16, 00161 Rome, Italy.
Noncoding RNA. 2022 Jul 1;8(4):50. doi: 10.3390/ncrna8040050.
Acute myeloid leukemia (AML) is a hematological malignancy originating from defective hematopoietic stem cells in the bone marrow. In spite of the recent approval of several molecular targeted therapies for AML treatment, disease recurrence remains an issue. Interestingly, increasing evidence has pointed out the relevance of bone marrow (BM) niche remodeling during leukemia onset and progression. Complex crosstalk between AML cells and microenvironment components shapes the leukemic BM niche, consequently affecting therapy responsiveness. Notably, circular RNAs are a new class of RNAs found to be relevant in AML progression and chemoresistance. In this review, we provided an overview of AML-driven niche remodeling. In particular, we analyzed the role of circRNAs and their possible contribution to cell-cell communication within the leukemic BM microenvironment. Understanding these mechanisms will help develop a more effective treatment for AML.
急性髓系白血病(AML)是一种起源于骨髓中造血干细胞缺陷的血液系统恶性肿瘤。尽管最近有几种分子靶向疗法获批用于AML治疗,但疾病复发仍然是一个问题。有趣的是,越来越多的证据指出了骨髓(BM)微环境重塑在白血病发生和进展过程中的相关性。AML细胞与微环境成分之间复杂的相互作用塑造了白血病BM微环境,从而影响治疗反应性。值得注意的是,环状RNA是一类新发现的与AML进展和化疗耐药相关的RNA。在本综述中,我们概述了由AML驱动的微环境重塑。特别是,我们分析了环状RNA的作用及其对白血病BM微环境中细胞间通讯的可能贡献。了解这些机制将有助于开发更有效的AML治疗方法。