Aziz Faisal, Chakraborty Abhijit, Khan Imran, Monts Josh
The Hormel Institute, University of Minnesota, Austin, MN 55912, USA.
Biology (Basel). 2022 Feb 6;11(2):249. doi: 10.3390/biology11020249.
In 1993, the discovery of microRNAs in () altered the paradigmatic view of RNA biology and post-transcriptional gene regulation. Further study revealed the role of microRNAs in disease development and progression. In particular, this review highlights microRNA-223 (miR-223 or miRNA-223) expression in malignant neoplastic disorders. miR-223 expression controls aspects of hematopoiesis and apoptosis, and cell proliferation, migration, and invasion. miR-223 regulates a number of gene targets, including cytoplasmic activation/proliferation-associated protein-1 (Caprin-1), insulin-like growth factor-1 receptor (IGF-1R), and other cell proliferation- and cell cycle-associated genes. Several studies have proposed miR-223 as a novel biomarker for early cancer diagnosis. Here, we emphasize miR-223's role in the development and progression of cancer.
1993年,在()中发现的微小RNA改变了RNA生物学和转录后基因调控的范式观点。进一步的研究揭示了微小RNA在疾病发生和发展中的作用。特别是,本综述重点介绍了微小RNA-223(miR-223或miRNA-223)在恶性肿瘤疾病中的表达。miR-223的表达控制造血、凋亡以及细胞增殖、迁移和侵袭等方面。miR-223调控多个基因靶点,包括细胞质激活/增殖相关蛋白-1(Caprin-1)、胰岛素样生长因子-1受体(IGF-1R)以及其他与细胞增殖和细胞周期相关的基因。多项研究提出将miR-223作为早期癌症诊断的新型生物标志物。在此,我们强调miR-223在癌症发生和发展中的作用。