Ranjan Prashant, Devi Chandra, Verma Neha, Bansal Rajesh, Srivastava Vinay Kumar, Das Parimal
Centre for Genetic Disorders, Institute of Science, Banaras Hindu University, Varanasi, UP, 221005, India.
Dentistry Oral Surgery and Medicine, Institute of Medical Sciences, Banaras Hindu University, Varanasi, UP, 221005, India.
Biochem Genet. 2025 Feb 22. doi: 10.1007/s10528-025-11064-9.
This study employs a comprehensive multi-omics approach to investigate the regulatory roles of specific microRNAs (miRNAs) in Congenital Tooth Agenesis (CTA). A total of 58 miRNAs associated with tooth diseases, cancer, and bone development were initially identified through a literature review and analyzed using bioinformatics. Based on target prediction and network analysis, eight miRNAs with strong connectivity and common target genes were shortlisted for further investigation. Blood samples from 10 CTA patients and 5 healthy controls were analyzed for miRNA expression using stem-loop RT-PCR. Four miRNAs-hsa-miR-218-5p, hsa-miR-15b-5p, hsa-miR-200b-3p, and hsa-let-7a-3p-were identified as significantly differentially expressed, marking their first reported involvement in CTA. Notably, hsa-miR-218-5p and hsa-let-7a-3p emerged as novel regulators with no prior associations with CTA or tooth development. To address the limitations of a small sample size, a multi-omics strategy was employed to validate these findings, integrating miRNA expression data with whole exome sequencing (WES), gene expression panels, and metabolomic profiling. The analysis confirmed the association of these four miRNAs with CTA and highlighted their involvement in critical biological pathways such as Wnt signaling, FGF signaling, and PI3 kinase pathways, which are essential for cellular proliferation, differentiation, and tissue morphogenesis. Importantly, the identification of these miRNAs in blood samples, rather than traditional dental tissues, highlights a minimally invasive approach that could aid in the early detection, therapeutic targeting, and personalized management of dental anomalies.
本研究采用综合多组学方法来探究特定微小RNA(miRNA)在先天性牙齿缺失(CTA)中的调控作用。通过文献综述初步鉴定出总共58种与牙齿疾病、癌症和骨骼发育相关的miRNA,并使用生物信息学进行分析。基于靶标预测和网络分析,筛选出8种具有强连通性和共同靶基因的miRNA进行进一步研究。使用茎环RT-PCR分析了10名CTA患者和5名健康对照的血液样本中的miRNA表达。鉴定出4种miRNA——hsa-miR-218-5p、hsa-miR-15b-5p、hsa-miR-200b-3p和hsa-let-7a-3p——有显著差异表达,这是它们首次被报道与CTA有关。值得注意的是,hsa-miR-218-5p和hsa-let-7a-3p是新型调控因子,此前与CTA或牙齿发育无关联。为解决样本量小的局限性,采用多组学策略来验证这些发现,将miRNA表达数据与全外显子测序(WES)、基因表达谱和代谢组学分析相结合。分析证实了这4种miRNA与CTA的关联,并突出了它们参与Wnt信号通路、FGF信号通路和PI3激酶通路等关键生物学途径,这些途径对细胞增殖、分化和组织形态发生至关重要。重要的是,在血液样本而非传统牙齿组织中鉴定出这些miRNA,突出了一种微创方法,该方法有助于牙齿异常的早期检测、治疗靶向和个性化管理。