Jiménez-Ortega Rogelio F, Ramírez-Salazar Eric G, Parra-Torres Alma Y, Muñoz-Montero Said A, Rangel-Escareňo Claudia, Salido-Guadarrama Ivan, Rodriguez-Dorantes Mauricio, Quiterio Manuel, Salmerón Jorge, Velázquez-Cruz Rafael
Genetics of Bone Metabolism Laboratory, National Institute of Genomic Medicine (INMEGEN), 14610 Mexico City, Mexico.
CONACYT, National Institute of Genomic Medicine (INMEGEN), 14610 Mexico City, Mexico.
Exp Ther Med. 2017 Dec;14(6):5464-5472. doi: 10.3892/etm.2017.5260. Epub 2017 Oct 3.
MicroRNAs (miRNAs or miRs) are a class of short non-coding RNAs that serve an important regulatory role in living organisms. These molecules are associated with multiple biological processes and are potential biomarkers in multiple diseases. The present study aimed to further identify miRNAs that are differentially expressed in circulating monocytes (CMCs) from postmenopausal Mexican-Mestizo women. Microarray analyses of monocytes using Affymetrix miRNA 4.0 and Human Genome U133 Plus 2.0 arrays were performed in 6 normal and 6 osteoporotic women, followed by reverse transcription-quantitative polymerase chain reaction (RT-qPCR) validation. The overexpression of miR-1270, miR-548×-3p and miR-8084 were detected in the osteoporosis compared with the normal group according to the microarray analysis; miR-1270, a miRNA with several target genes associated with bone remodeling, was validated by RT-qPCR. Bioinformatics analysis identified that interferon regulatory factor 8 () is the most likely target gene of miR-1270, which is associated with osteoclastogenesis. Furthermore, the findings of the present study demonstrate that an upregulation of miR-1270 may reduce the gene expression of in CMCs (osteoclast precursors), implicating its potential role in leading to low bone mineral density and contributing to osteoporosis development in postmenopausal women.
微小RNA(miRNA或miR)是一类短链非编码RNA,在生物体中发挥重要的调节作用。这些分子与多种生物学过程相关,是多种疾病的潜在生物标志物。本研究旨在进一步鉴定在绝经后墨西哥梅斯蒂索女性循环单核细胞(CMC)中差异表达的miRNA。使用Affymetrix miRNA 4.0和人类基因组U133 Plus 2.0芯片对6名正常女性和6名骨质疏松女性的单核细胞进行微阵列分析,随后进行逆转录定量聚合酶链反应(RT-qPCR)验证。根据微阵列分析,与正常组相比,骨质疏松组中检测到miR-1270、miR-548×-3p和miR-8084的过表达;miR-1270是一种与多个骨重塑相关靶基因的miRNA,通过RT-qPCR验证。生物信息学分析确定干扰素调节因子8()是miR-1270最可能的靶基因,其与破骨细胞生成相关。此外,本研究结果表明,miR-1270的上调可能会降低CMC(破骨细胞前体)中该基因的表达,暗示其在导致绝经后女性骨密度降低和促成骨质疏松症发展中的潜在作用。