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DC Field | Value | Language |
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dc.contributor.author | Jirawechwongsakul P. | |
dc.contributor.author | Taebunpakul P. | |
dc.contributor.author | Pavasant P. | |
dc.date.accessioned | 2022-12-14T03:16:54Z | - |
dc.date.available | 2022-12-14T03:16:54Z | - |
dc.date.issued | 2022 | |
dc.identifier.issn | 25869981 | |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85139507718&doi=10.31584%2fjhsmr.2022876&partnerID=40&md5=eb71da48d5142472557864436c220383 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/27120 | - |
dc.description.abstract | Objective: 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.language | en | |
dc.publisher | Prince of Songkla University | |
dc.subject | basic fibroblast growth factor | |
dc.subject | cell cycle | |
dc.subject | cell proliferation | |
dc.subject | human dental pulp cells | |
dc.subject | let-7 microRNA | |
dc.title | Effect of Basic Fibroblast Growth Factor on Expression of Let-7 MicroRNA in Proliferation of Human Dental Pulp Cells | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Oman Medical Journal. Vol 37, No.6 (2022) | |
dc.identifier.doi | 10.31584/jhsmr.2022876 | |
Appears in Collections: | Scopus 2022 |
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