Jalili Mohammadmahdi, Tavakoli Setayesh, Kargar Kamran, Rafat Milad, Rad Fatemeh R
Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Department of Prosthodontics, Shahed Medical University, Tehran, Iran.
Adv Biomed Res. 2023 Jun 30;12:170. doi: 10.4103/abr.abr_369_22. eCollection 2023.
MicroRNAs are a large group of small, non-coding ssRNAs (miRNAs) that have an epigenetically pivotal role in gene expression and other biological processes in cells and can be regarded as capable biomarkers for the early detection and management of cancer. The aim of the present review article is to summarize the evidence for recognizing the molecular mechanism, target genes, and clinical significance of miR-647 in different cancers. Multiple studies have demonstrated that aberrant expression of miR-647 could be found in a variety of malignancies, such as bladder cancer, cervical cancer, colorectal cancer, gastric cancer, glioma, hepatocellular carcinoma, non-small cell lung cancer, ovarian cancer, and prostate cancer have reported, notably, increase or decrease in expression of miR-647 so that it can function as a tumorigenic (oncomiR) or tumor suppressor gene. MiR-647 is effective in the proliferation, migration, and invasion of cancer cells by playing a function in cell cycle pathways. MiR-647 can be a valuable potential biomarker for assessing the extent of cancer, prognosis, and response to therapy and shows great therapeutic efficacy in different solid tumors. Moreover, serum concentrations of miR-647 are directly effective in decreasing overall survival and disease progression. So, an efficient therapeutic target can be the effect on miR-647 expression by antitumor drugs.
微小RNA是一大类小的非编码单链RNA(miRNA),它们在细胞的基因表达和其他生物学过程中具有关键的表观遗传作用,可被视为癌症早期检测和管理的潜在生物标志物。本综述文章的目的是总结有关识别miR-647在不同癌症中的分子机制、靶基因和临床意义的证据。多项研究表明,在多种恶性肿瘤中可发现miR-647表达异常,如膀胱癌、宫颈癌、结直肠癌、胃癌、神经胶质瘤、肝细胞癌、非小细胞肺癌、卵巢癌和前列腺癌,值得注意的是,miR-647表达的增加或减少使其可作为致癌基因(致癌miRNA)或肿瘤抑制基因发挥作用。MiR-647通过在细胞周期途径中发挥作用,对癌细胞的增殖、迁移和侵袭具有影响。MiR-647可能是评估癌症程度、预后和治疗反应的有价值的潜在生物标志物,并且在不同实体瘤中显示出巨大的治疗效果。此外,miR-647的血清浓度直接影响总生存期和疾病进展。因此,一个有效的治疗靶点可能是抗肿瘤药物对miR-647表达的影响。