Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/27120
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dc.contributor.authorJirawechwongsakul P.
dc.contributor.authorTaebunpakul P.
dc.contributor.authorPavasant P.
dc.date.accessioned2022-12-14T03:16:54Z-
dc.date.available2022-12-14T03:16:54Z-
dc.date.issued2022
dc.identifier.issn25869981
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85139507718&doi=10.31584%2fjhsmr.2022876&partnerID=40&md5=eb71da48d5142472557864436c220383
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/27120-
dc.description.abstractObjective: Basic fibroblast growth factor (bFGF) plays a pivotal role in cell proliferation, differentiation and extracellular matrix turnover in various tissues. In human dental pulp cells (HDPCs), let-7 microRNA is involved in cell proliferation and differentiation. There is little information on the effect of bFGF-induced cell proliferation on let-7 microRNA in HDPCs. This study investigated the effect of bFGF on let-7g, let-7f, and let-7i microRNAs and some of the genes involved in cell proliferation including p53 and Ki67 in HDPCs. Material and Methods: HDPCs were cultured and treated with bFGF at 0, 1, and 5 ng/mL. Cell proliferation was examined using the 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay at 24 and 48 hours. Additionally, gene expressions of let-7g, let-7f, let-7i microRNAs, and p53 and Ki67 were examined by quantitative real-time polymerase chain reaction at 24 hours. All experiments were performed in triplicate. Results: The results showed that let-7g, let-7f, and let-7i microRNAs were expressed in HDPCs. MTT assays showed that bFGF induced greater cell proliferation than the controls at 24 and 48 hours (p-value<0.050). HDPCs treated with bFGF showed a decrease in p53 expression (p-value<0.001) while Ki67 expression increased (p-value<0.001). The expression of let-7g microRNA decreased under the influence of bFGF (p-value<0.050). However, bFGF had no effect on expression of let-7f and let-7i microRNAs (p-value>0.050). Conclusion: Our preliminary study showed that exogenous bFGF could decrease let-7g microRNA expression suggesting that let-7g microRNA may be involved in bFGF-induced HDPCs proliferation. © 2022 JHSMR. Hosting by Prince of Songkla University. All rights reserved.
dc.languageen
dc.publisherPrince of Songkla University
dc.subjectbasic fibroblast growth factor
dc.subjectcell cycle
dc.subjectcell proliferation
dc.subjecthuman dental pulp cells
dc.subjectlet-7 microRNA
dc.titleEffect of Basic Fibroblast Growth Factor on Expression of Let-7 MicroRNA in Proliferation of Human Dental Pulp Cells
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationOman Medical Journal. Vol 37, No.6 (2022)
dc.identifier.doi10.31584/jhsmr.2022876
Appears in Collections:Scopus 2022

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