Cárdenas-Bedoya Jhonathan, Marquez-Pedroza Jazmin, Morán-Moguel María Cristina, Escoto-Delgadillo Martha, Vázquez-Valls Eduardo, González-Enríquez Gracia Viviana, Pérez-Ríos Alma Minerva, Torres-Mendoza Blanca Miriam
Instituto Mexicano del Seguro Social, Centro de Investigación Biomédica de Occidente, Laboratorio de Inmunodeficiencias y Retrovirus Humanos, Guadalajara, Jalisco, Mexico.
Universidad de Guadalajara, Departamento de Biología Molecular y Genómica, Guadalajara, Jalisco, Mexico.
Genet Mol Biol. 2020 Jun 22;43(3):e20200017. doi: 10.1590/1678-4685-GMB-2020-0017. eCollection 2020.
MicroRNAs are considered as potential biomarkers, agents, or therapeutic targets; few studies have addressed the expression of miRNAs in treatment-naïve patients infected with HIV-1. The aim of this study was to assess plasma relative circulating miRNA expression profiles in treatment-naïve Mexican patients with HIV/AIDS and healthy individuals using a commercial array. A low CD4+ T cell count and high viral load were found in all patients. Decreased relative miRNA-296-5p expression was observed in patients; moreover, this was the only miRNA that showed differences between the two groups. Thus, we measured the absolute expression of miR-296-5p by qPCR, confirming the result with statistically significant differences (P < 0.05). There is evidence that miR-296-5p regulates the expression of the PIN1 gene, which encodes the peptidylprolyl Cis/Trans isomerase NIMA-Interacting-1, that is involved in different stages of the biological cycle of HIV-1, this relationship is corroborated by bioinformatics analysis and ELISA assay was used to measure plasma levels of PIN1. The decreased expression of miR-296-5p found in naïve patients with HIV infection suggests a regulatory activity of this miRNA on virus replication, making it a potential therapeutic agent against HIV. Finally, miR-296-5p could be inhibiting the virus transcription by regulating genes different than PIN1.
微小RNA被认为是潜在的生物标志物、药物或治疗靶点;很少有研究探讨过微小RNA在未接受治疗的HIV-1感染患者中的表达情况。本研究的目的是使用商业芯片评估未接受治疗的墨西哥HIV/AIDS患者和健康个体血浆中相对循环微小RNA的表达谱。所有患者均发现CD4+T细胞计数低且病毒载量高。在患者中观察到相对微小RNA-296-5p表达降低;此外,这是两组之间唯一表现出差异的微小RNA。因此,我们通过qPCR测量了miR-296-5p的绝对表达,结果具有统计学显著差异(P<0.05)。有证据表明miR-296-5p调节PIN1基因的表达,该基因编码肽基脯氨酰顺/反异构酶NIMA相互作用蛋白1,其参与HIV-1生物周期的不同阶段,生物信息学分析证实了这种关系,并使用ELISA测定法测量血浆中PIN1的水平。在未接受治疗的HIV感染患者中发现的miR-296-5p表达降低表明该微小RNA对病毒复制具有调节活性,使其成为一种潜在的抗HIV治疗药物。最后,miR-296-5p可能通过调节不同于PIN1的基因来抑制病毒转录。