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miR-142-3p 在口腔扁平苔藓中的临床意义及其对角质形成细胞增殖的调控作用。

Clinical significance of miR-142-3p in oral lichen planus and its regulatory role in keratinocyte proliferation.

机构信息

Department of Dermatology, Guangrao People's Hospital, Shandong, China.

Department of Dermatology, Linyi City Lanshan District People's Hospital, Linyi, Shandong, China.

出版信息

Oral Surg Oral Med Oral Pathol Oral Radiol. 2021 Oct;132(4):441-447. doi: 10.1016/j.oooo.2021.06.008. Epub 2021 Jun 20.

Abstract

OBJECTIVE

Accumulating microRNAs (miRNAs) have been identified as aberrantly expressed in patients with oral lichen planus (OLP). This study aimed to investigate the role and underlying mechanism of miR-142-3p in OLP.

STUDY DESIGN

Fifty-six patients with OLP and 44 control participants without OLP were recruited, and real-time quantitative reverse transcription polymerase chain reaction was used for the measurement of miR-142-3p. A receiver operating characteristic (ROC) was counted to assess the diagnostic value. Cell Counting Kit‑8 was used to assess cell proliferation. The luciferase reporter assay was performed to confirm the target gene.

RESULTS

Compared with the control group, an elevated expression of miR-142-3p was detected in the serum, saliva, and tissues samples from patients with OLP. ROC curve analysis suggested that miR-142-3p could distinguish patients with OLP from those in the control group, and the expression of miR-142-3p was closely associated with the disease severity. Downregulation of miR-142-3p inhibited keratinocyte proliferation. Glucocorticoid receptor α (GRα) was a target gene of miR-142-3p.

CONCLUSIONS

MiR-142-3p might be a candidate diagnostic biomarker for OLP. Downregulation of miR-142-3p inhibits keratinocyte proliferation, and GRα might be involved in its regulatory role.

摘要

目的

越来越多的 microRNAs(miRNAs)被鉴定为口腔扁平苔藓(OLP)患者中异常表达。本研究旨在探讨 miR-142-3p 在 OLP 中的作用及其潜在机制。

研究设计

招募了 56 名 OLP 患者和 44 名无 OLP 的对照参与者,并使用实时定量逆转录聚合酶链反应测量 miR-142-3p。计算受试者工作特征(ROC)曲线以评估诊断价值。使用细胞计数试剂盒-8 评估细胞增殖。进行荧光素酶报告基因检测以验证靶基因。

结果

与对照组相比,OLP 患者的血清、唾液和组织样本中检测到 miR-142-3p 的表达升高。ROC 曲线分析表明,miR-142-3p 可区分 OLP 患者和对照组,且 miR-142-3p 的表达与疾病严重程度密切相关。下调 miR-142-3p 抑制角质形成细胞增殖。糖皮质激素受体α(GRα)是 miR-142-3p 的靶基因。

结论

miR-142-3p 可能是 OLP 的候选诊断生物标志物。下调 miR-142-3p 抑制角质形成细胞增殖,GRα 可能参与其调节作用。

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