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Decreased expression of the m6A RNA methyltransferase METTL3 is associated with residual ridge resorption

OBJECTIVE: N6-methyladenosine (m6A) methylation and its regulators play crucial roles in the progression of osteoporosis (OP) by regulating the expression of osteoporosis-related genes. In this study, we have analyzed the expression of methyltransferase-like 3 (METTL3) and its target gene Runt-relat...

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Detalles Bibliográficos
Autores principales: Krishnamoorthy, Harini Sri, Kannan, Balachander, Ganapathy, Dhanraj, Jayaseelan, Vijayashree Priyadharsini, Arumugam, Paramasivam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10407425/
https://www.ncbi.nlm.nih.gov/pubmed/37559689
http://dx.doi.org/10.1016/j.jobcr.2023.07.003
Descripción
Sumario:OBJECTIVE: N6-methyladenosine (m6A) methylation and its regulators play crucial roles in the progression of osteoporosis (OP) by regulating the expression of osteoporosis-related genes. In this study, we have analyzed the expression of methyltransferase-like 3 (METTL3) and its target gene Runt-related transcription factor 2 (RUNX2) in patients with residual ridge resorption (RRR). MATERIALS AND METHODS: A total 50 number of participants were included in this comparative study (RRR – n25 and healthy control – n25). Total RNA was extracted from peripheral blood and converted into cDNA. METTL3 and RUNX2 expression levels were quantified using RT-qPCR with GAPDH as the reference gene. Bioinformatics tools were used to identify gene functions and pathways. RESULTS: Real-time polymerase chain reaction (qPCR) revealed that METTL3 and RUNX2 expression was downregulated in the RRR group compared to that in healthy controls (P < 0.05). In silico functional analysis provided information regarding the role of METTL3 in various biological processes. CONCLUSION: Our findings suggest that METTL3 dysregulation contributes to RRR pathogenesis. Further large-scale samples and functional studies are required to identify their therapeutic potential.