Laboratory of Human and Medical Genetics, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.
Postgraduate Program in Genetics and Molecular Biology, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.
J Oral Pathol Med. 2020 Mar;49(3):201-209. doi: 10.1111/jop.12950. Epub 2019 Sep 17.
Orofacial clefts are facial malformations caused by the improper development of the lips and palate. Many genetic and epigenetic molecules have been involved in the mechanisms of orofacial clefts, one of which are miRNAs. This systematic review aimed to identify miRNAs associated to non-syndromic orofacial clefts in humans. After applying a series of criteria, four studies were selected for analysis. In total, one hundred miRNAs were observed in the literature, of which 57 were reported as upregulated and 43 as downregulated in all orofacial cleft classifications. Moreover, nine miRNAs were differentially expressed only in cleft palate patients, which might suggest distinct regulatory mechanisms for the etiology of cleft lips and palates. We suggest broader population sampling in order to include diverse ethnic groups in the future, as well as analyses toward identifying miRNA target genes and pathways. We highlight the need for experimental validation and of these results to allow further translational approaches and clinical applications.
口腔面裂是由嘴唇和 palate 的不正常发育引起的面部畸形。许多遗传和表观遗传分子参与了口腔面裂的发生机制,其中之一是 miRNAs。本系统综述旨在确定与人类非综合征性口腔面裂相关的 miRNAs。经过一系列标准的应用,有四项研究被选中进行分析。总共在文献中观察到一百种 miRNAs,其中 57 种在所有口腔面裂分类中被报道为上调,43 种为下调。此外,有 9 种 miRNAs 仅在腭裂患者中表达差异,这可能提示唇裂和腭裂病因的不同调节机制。我们建议更广泛的人群采样,以便在未来纳入不同的种族群体,以及分析识别 miRNA 靶基因和途径。我们强调需要对这些结果进行实验验证,以允许进一步的转化方法和临床应用。