微RNA抑制转移和细胞增殖及其在OSCC中的潜在治疗应用:系统综述。

IF 2.9 4区 医学 Q2 PATHOLOGY Pathology, research and practice Pub Date : 2024-08-11 DOI:10.1016/j.prp.2024.155532
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引用次数: 0

摘要

背景和目的:口腔鳞状细胞癌(OSCC)是世界上恶性程度最高的癌症之一,死亡率很高。由于微小RNA(miRNA)在包括OSCC在内的各种癌症的发病和维持过程中的作用,它们逐渐受到人们的关注。在这项研究中,我们进行了一项范围综述,分析了miRNA在OSCC中的作用和治疗反应,并重点研究了与miRNA相关的抑制OSCC转移和细胞增殖的靶轴:本综述遵循六阶段方法框架和 PRISMA 指南。系统检索了三个数据库,以找到截至 2024 年 7 月符合条件的文章。两名审稿人独立进行了文章筛选和数据提取。成功确定了 54 篇符合预定义纳入标准的文章。采用牙科体外研究专用的 QUIN 检查表进行了质量评估:不同设计的研究报告了 53 种 miRNA,这些 miRNA 经实验验证可作为 OSCC 体内和体外研究的治疗靶点。研究发现,有 25 个 miRNA 在 OSCC 患者和细胞系中上调,另有 25 个下调。在两项不同的研究中,Mir-186也被发现上调和下调。研究强调了六种 microRNA(miR-32-5p、miR-195-5p、miR-3529-3p、miR-191、miR-146b-5p 和 miR-377-3p)作为抗肿瘤增殖、迁移和侵袭疗法治疗 OSCC 的潜力。两个 miRNA(miR-302b 和 miR-18a)被确定为抗转移疗法,而四个 miRNA(miR-617、miR-23a-3p、miR-105 和 miR-101)则是抗增殖疗法:研究建议,恢复肿瘤抑制miRNA的表达可能是一种合适的癌症疗法。利用这种技术确实存在一些困难,解决这些困难将改进向靶细胞转移 miRNA 的方法。随着研究的深入和相关问题的解决,miRNA 将成为治疗 OSCC 的有效方法。
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Metastasis and cell proliferation inhibition by microRNAs and its potential therapeutic applications in OSCC: A systematic review

Background and Aims

Oral squamous cell carcinoma (OSCC) is among the most malignant cancers in the world and has a high mortality rate. MicroRNAs (miRNAs) have progressively gained attention due to their roles in the pathogenesis and maintenance of various kinds of cancers, including OSCC. In this research, we carried out a scoping review to analyze the role of miRNA and therapeutic response in OSCC and focus on target axes associated with miRNA that inhibit metastasis and cell proliferation in OSCC.

Methods

This review adhered to a six-stage methodology framework and PRISMA guidelines. Three databases were systematically searched to find eligible articles until July 2024. Two reviewers conducted publication screening and data extraction independently. 54 articles meeting the predefined inclusion criteria were successfully identified. Quality assessment was done using the QUIN checklist specified for dental in vitro studies.

Results

Studies with different designs reported 53 miRNAs that were experimentally validated to act as therapeutic targets in OSCC in vivo and in vitro studies. The study found that 25 miRNAs were up-regulated in OSCC patients and cell lines, while another 25 were down-regulated. Mir-186 was also found to be up- and down-regulated in two different investigations. The study highlights the potential of six microRNAs (miR-32–5p, miR-195–5p, miR-3529–3p, miR-191, miR-146b-5p, and miR-377–3p) as anti-proliferation, migration, and invasion therapeutics for OSCC treatment. Two miRNAs (miR-302b and miR-18a) are identified as anti-metastatic therapeutics, while four miRNAs (miR-617, miR-23a-3p, miR-105, miR-101) are anti-proliferation therapeutics.

Conclusion

The study recommends that restoring the expression of tumor suppressor miRNAs may be a suitable cancer therapy. Utilizing this technology does present certain difficulties, and resolving them will improve the methods for miRNA transfer to target cells. With more research and the resolution of associated issues, miRNA can be employed as an efficient therapeutic method for OSCC.

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来源期刊
CiteScore
5.00
自引率
3.60%
发文量
405
审稿时长
24 days
期刊介绍: Pathology, Research and Practice provides accessible coverage of the most recent developments across the entire field of pathology: Reviews focus on recent progress in pathology, while Comments look at interesting current problems and at hypotheses for future developments in pathology. Original Papers present novel findings on all aspects of general, anatomic and molecular pathology. Rapid Communications inform readers on preliminary findings that may be relevant for further studies and need to be communicated quickly. Teaching Cases look at new aspects or special diagnostic problems of diseases and at case reports relevant for the pathologist''s practice.
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