• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Mir-let-7a在口腔鳞状细胞癌和口腔扁平苔藓中的差异表达:早期诊断生物标志物开发的见解

Mir-let-7a Differential Expression in Oral Squamous Cell Carcinoma and Oral Lichen Planus: Insights for Early Diagnostic Biomarker Development.

作者信息

Seyedhoseini Seyedmovahed, Mohtasham Nooshin, Saghafi Shadi, Alahkhani Negin, Mohajertehran Farnaz, Afzaljavan Fahimeh, Shakeri Mahammad Taghi, Bokharaei Amirkian

机构信息

Dental Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Oral and Maxillofacial Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

出版信息

Rep Biochem Mol Biol. 2025 Jan;13(4):456-465. doi: 10.61186/rbmb.13.4.456.

DOI:10.61186/rbmb.13.4.456
PMID:40842903
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12367217/
Abstract

BACKGROUND

Early detection of oral squamous cell carcinoma (OSCC) is essential for improving treatment outcomes. Oral lichen planus (OLP) is recognized as a premalignant condition that may progress to OSCC. Recently, microRNAs, particularly miR-let-7a, have emerged as promising biomarkers for gene regulation and early disease diagnosis. This study aimed to evaluate the expression level of miR-let-7a in OSCC and OLP patients, and to compare it with healthy controls, to determine its potential as an early diagnostic marker.

METHODS

In this cross-sectional study, serum samples were collected from 36 OSCC patients, 38 OLP patients, and 38 healthy controls. Diagnosis of OSCC and OLP was confirmed via biopsy. Serum RNA was isolated, and after quality verification, cDNA was synthesized. Quantitative real-time PCR (qRT-PCR) was performed to assess miR-let-7a expression across the three groups. Statistical analysis was conducted using SPSS version 16.0.

RESULTS

Significant differences in miR-let-7a expression were observed among the groups. Mean expression levels of miR-let-7a were 1.55 ± 1.19 in OSCC, 2.97 ± 2.00 in OLP, and 7.02 ± 4.10 in the control group (p< 0.001). Lower miR-let-7a expression in OSCC was notably correlated with adverse clinicopathological features, including higher tumor grade (p < 0.001), advanced clinical stage (p= 0.011), larger tumor size (T2) (p< 0.0001), and lymph node involvement (p< 0.0001).

CONCLUSIONS

The findings demonstrate that miR-let-7a expression is significantly reduced in OSCC and OLP patients compared to healthy controls, highlighting its potential as an early biomarker for detecting malignant transformation in oral lesions and understanding disease progression in OSCC and OLP.

摘要

背景

早期发现口腔鳞状细胞癌(OSCC)对于改善治疗效果至关重要。口腔扁平苔藓(OLP)被认为是一种可能进展为OSCC的癌前病变。最近,微小RNA,特别是miR-let-7a,已成为基因调控和疾病早期诊断的有前景的生物标志物。本研究旨在评估miR-let-7a在OSCC和OLP患者中的表达水平,并与健康对照进行比较,以确定其作为早期诊断标志物的潜力。

方法

在这项横断面研究中,收集了36例OSCC患者、38例OLP患者和38例健康对照的血清样本。通过活检确诊OSCC和OLP。分离血清RNA,经质量验证后合成cDNA。采用定量实时PCR(qRT-PCR)评估三组中miR-let-7a的表达。使用SPSS 16.0版进行统计分析。

结果

各组间miR-let-7a表达存在显著差异。OSCC组miR-let-7a的平均表达水平为1.55±1.19,OLP组为2.97±2.00,对照组为7.02±4.10(p<0.001)。OSCC中较低的miR-let-7a表达与不良临床病理特征显著相关,包括更高的肿瘤分级(p<0.001)、晚期临床分期(p=0.011)、更大的肿瘤大小(T2)(p<0.0001)和淋巴结受累(p<0.0001)。

结论

研究结果表明,与健康对照相比,OSCC和OLP患者中miR-let-7a表达显著降低,突出了其作为检测口腔病变恶性转化以及了解OSCC和OLP疾病进展的早期生物标志物的潜力。

相似文献

1
Mir-let-7a Differential Expression in Oral Squamous Cell Carcinoma and Oral Lichen Planus: Insights for Early Diagnostic Biomarker Development.Mir-let-7a在口腔鳞状细胞癌和口腔扁平苔藓中的差异表达:早期诊断生物标志物开发的见解
Rep Biochem Mol Biol. 2025 Jan;13(4):456-465. doi: 10.61186/rbmb.13.4.456.
2
Unveiling the Potential of Serum MiR-483-5p: A Promising Diagnostic and Prognostic Biomarker in OLP and OSCC Patients by Analysis of Differential Gene Expression.揭示血清 miR-483-5p 的潜力:通过差异基因表达分析,作为 OLp 和 OSCC 患者的有前途的诊断和预后生物标志物。
Curr Pharm Des. 2024;30(4):310-322. doi: 10.2174/0113816128276149240108163407.
3
Long non-coding RNAs PVT1, CCAT2, and TCF7L2, and miR-33 and c-Myc expression in oral squamous cell carcinoma and oral lichen planus patients.长链非编码RNA PVT1、CCAT2和TCF7L2以及miR-33和c-Myc在口腔鳞状细胞癌和口腔扁平苔藓患者中的表达。
J Craniomaxillofac Surg. 2025 Aug;53(8):1197-1204. doi: 10.1016/j.jcms.2025.04.006. Epub 2025 May 12.
4
Demographic and Clinical Characteristics of Patients With Oral Lichen Planus in a Cohort From Casablanca, Morocco.摩洛哥卡萨布兰卡一组口腔扁平苔藓患者的人口统计学和临床特征
Cureus. 2025 Jun 30;17(6):e87015. doi: 10.7759/cureus.87015. eCollection 2025 Jun.
5
Low Incidence of Oral Squamous Cell Carcinoma in Patients With Oral Lichen Planus on Sustained Anti-Inflammatory Therapy: A Single-Centre Retrospective Study of 273 Patients.接受持续抗炎治疗的口腔扁平苔藓患者口腔鳞状细胞癌的低发病率:一项对273例患者的单中心回顾性研究
J Cutan Med Surg. 2025 Jul-Aug;29(4):369-373. doi: 10.1177/12034754251324945. Epub 2025 Mar 25.
6
The malignant transformation of oral lichen planus and oral lichenoid lesions: a systematic review.口腔扁平苔藓和口腔苔藓样病变的恶性转化:一项系统评价。
J Am Dent Assoc. 2014 Jan;145(1):45-56. doi: 10.14219/jada.2013.10.
7
Crossroads between Skin and Endocrine Glands: The Interplay of Lichen Planus with Thyroid Anomalies.皮肤与内分泌腺的交叉点:扁平苔藓与甲状腺异常的相互作用
Biomedicines. 2023 Dec 28;12(1):77. doi: 10.3390/biomedicines12010077.
8
Interventions for treating oral lichen planus.治疗口腔扁平苔藓的干预措施。
Cochrane Database Syst Rev. 2011 Jul 6(7):CD001168. doi: 10.1002/14651858.CD001168.pub2.
9
Immunohistochemical Assessment of Maspin, β-Catenin, and MMP-14 in Oral Potentially Malignant Lesions and Oral Squamous Cell Carcinoma: A Retrospective Observational Study.口腔潜在恶性病变和口腔鳞状细胞癌中maspin、β-连环蛋白和基质金属蛋白酶-14的免疫组织化学评估:一项回顾性观察研究。
Medicina (Kaunas). 2025 Jun 4;61(6):1037. doi: 10.3390/medicina61061037.
10
Clinical value and potential circulating of miR-99a as tumor suppressor biomarker in serum of oral squamous cell carcinoma and erosive atrophic lichen planus.miR-99a 在口腔鳞状细胞癌和糜烂型扁平苔藓血清中的抑癌作用及其循环的临床价值。
J Stomatol Oral Maxillofac Surg. 2024 Jun;125(3S):101806. doi: 10.1016/j.jormas.2024.101806. Epub 2024 Feb 24.

本文引用的文献

1
Association of lncRNA ANRIL rs10757278 A>G Variant, Tumor Size, Grading, Tumor Site, and Tumor Stage in Oral Squamous Cell Carcinoma Patients.lncRNA ANRIL rs10757278 A>G变异与口腔鳞状细胞癌患者肿瘤大小、分级、肿瘤部位及肿瘤分期的相关性
Rep Biochem Mol Biol. 2024 Apr;13(1):59-66. doi: 10.61186/rbmb.13.1.59.
2
A pilot study to evaluate the expression of microRNA‑let‑7a in patients with intestinal‑type sinonasal adenocarcinoma.一项评估微小RNA-let-7a在肠型鼻窦腺癌患者中表达情况的试点研究。
Oncol Lett. 2023 Dec 20;27(2):69. doi: 10.3892/ol.2023.14202. eCollection 2024 Feb.
3
MicroRNA Let-7a association with glycolysis-induced autophagy in locally advanced gastric cancer: Their role in prognosis and FLOT chemotherapy resistance.miRNA Let-7a 与局部进展期胃癌糖酵解诱导自噬的关系:在预后和 FLOT 化疗耐药中的作用。
Pathol Res Pract. 2024 Jan;253:154968. doi: 10.1016/j.prp.2023.154968. Epub 2023 Nov 24.
4
Serum and Saliva Level of miR-31-5p and miR-let 7a in EBV Associated Oropharyngeal Cancer.EBV 相关口咽癌中 miR-31-5p 和 miR-let 7a 的血清及唾液水平
Int J Mol Sci. 2023 Jul 26;24(15):11965. doi: 10.3390/ijms241511965.
5
Circulating miRNA as a Biomarker in Oral Cancer Liquid Biopsy.循环微RNA作为口腔癌液体活检中的生物标志物
Biomedicines. 2023 Mar 21;11(3):965. doi: 10.3390/biomedicines11030965.
6
Pathway expression analysis.通路表达分析。
Sci Rep. 2022 Dec 17;12(1):21839. doi: 10.1038/s41598-022-26381-x.
7
The Functional Mechanism of MicroRNA in Oral Lichen Planus.微小RNA在口腔扁平苔藓中的作用机制
J Inflamm Res. 2022 Jul 26;15:4261-4274. doi: 10.2147/JIR.S369304. eCollection 2022.
8
Study on the mechanism of let-7a-5p in regulating the proliferation in cervical cancer cells.研究 let-7a-5p 调节宫颈癌细胞增殖的机制。
Clin Transl Oncol. 2022 Aug;24(8):1631-1642. doi: 10.1007/s12094-022-02810-1. Epub 2022 Mar 18.
9
New AKT-dependent mechanisms of anti-COVID-19 action of high-CBD Cannabis sativa extracts.高CBD含量大麻提取物抗COVID-19作用的新的依赖AKT的机制
Cell Death Discov. 2022 Mar 11;8(1):110. doi: 10.1038/s41420-022-00876-y.
10
Plasma cell-free RNA characteristics in COVID-19 patients.新型冠状病毒肺炎患者血浆游离 RNA 特征。
Genome Res. 2022 Feb;32(2):228-241. doi: 10.1101/gr.276175.121. Epub 2022 Jan 21.