Farc Ovidiu, Budisan Liviuta, Zaharie Florin, Țăulean Roman, Vălean Dan, Talvan Elena, Neagoe Ioana Berindan, Zănoagă Oana, Braicu Cornelia, Cristea Victor
Research Center for Functional Genomics, Biomedicine and Translational Medicine "Iuliu Hatieganu" University of Medicine and Pharmacy, 400337 Cluj-Napoca, Romania.
Surgical Department, "Iuliu Hatieganu" University of Medicine and Pharmacy, 400347 Cluj-Napoca, Romania.
Curr Issues Mol Biol. 2024 Jul 5;46(7):7065-7085. doi: 10.3390/cimb46070421.
Micro-RNAs (miRNAs) are non-coding RNAs with importance in the development of cancer. They are involved in both tumor development and immune processes in tumors. The present study aims to characterize the behavior of two miRNAs, the proinflammatory miR-326-5p and the anti-inflammatory miR-146a-5p, in colorectal cancer (CRC), to decipher the mechanisms that regulate their expression, and to study potential applications. Tissue levels of miR-326-5p and miR-146a-5p were determined by qrt-PCR (real-time quantitative reverse transcription polymerase chain reaction) in 45 patients with colorectal cancer in tumoral and normal adjacent tissue. Subsequent bioinformatic analysis was performed to characterize the transcriptional networks that control the expression of the two miRNAs. The biomarker potential of miRNAs was assessed. The expression of miR-325-5p and miR-146a-5p was decreased in tumors compared to normal tissue. The two miRNAs are regulated through a transcriptional network, which originates in the inflammatory and proliferative pathways and regulates a set of cellular functions related to immunity, proliferation, and differentiation. The miRNAs coordinate distinct modules in the network. There is good biomarker potential of miR-326 with an AUC (Area under the curve) of 0.827, 0.911 sensitivity (Sn), and 0.689 specificity (Sp), and of the combination miR-326-miR-146a, with an AUC of 0.845, Sn of 0.75, and Sp of 0.89. The miRNAs are downregulated in the tumor tissue. They are regulated by a transcriptional network in which they coordinate distinct modules. The structure of the network highlights possible therapeutic approaches. MiR-326 and the combination of the two miRNAs may serve as biomarkers in CRC.
微小RNA(miRNA)是一类非编码RNA,在癌症发展过程中具有重要作用。它们参与肿瘤的发生发展以及肿瘤中的免疫过程。本研究旨在表征两种miRNA,即促炎性miR-326-5p和抗炎性miR-146a-5p在结直肠癌(CRC)中的行为,解读调控其表达的机制,并研究其潜在应用。通过qrt-PCR(实时定量逆转录聚合酶链反应)测定了45例结直肠癌患者肿瘤组织及相邻正常组织中miR-326-5p和miR-146a-5p的组织水平。随后进行了生物信息学分析,以表征控制这两种miRNA表达的转录网络。评估了miRNA作为生物标志物的潜力。与正常组织相比,肿瘤中miR-325-5p和miR-146a-5p的表达降低。这两种miRNA通过一个转录网络进行调控,该网络起源于炎症和增殖途径,并调控一组与免疫、增殖和分化相关的细胞功能。这些miRNA在网络中协调不同的模块。miR-326具有良好的生物标志物潜力,曲线下面积(AUC)为0.827,灵敏度(Sn)为0.911,特异性(Sp)为0.689;miR-326-miR-146a组合的AUC为0.845,Sn为0.75,Sp为0.89。这些miRNA在肿瘤组织中表达下调。它们由一个转录网络调控,在该网络中它们协调不同的模块。网络结构突出了可能的治疗方法。MiR-326以及这两种miRNA的组合可能作为结直肠癌的生物标志物。