Suppr超能文献

口腔鳞状细胞癌中通过遗传与表观遗传的策略性桥接来综述疾病特异性 microRNAs

Review of Disease-Specific microRNAs by Strategically Bridging Genetics and Epigenetics in Oral Squamous Cell Carcinoma.

机构信息

Unit of Orofacial Genetics, 1st Department of Pediatrics, National Kapodistrian University of Athens, "Aghia Sophia" Children's Hospital, 115 27 Athens, Greece.

Department of Molecular Genetics, Cephalogenetics Center, 176 72 Athens, Greece.

出版信息

Genes (Basel). 2023 Aug 2;14(8):1578. doi: 10.3390/genes14081578.

Abstract

Oral squamous cell carcinoma (OSCC) is one of the most prevalent human malignancies and a global health concern with a poor prognosis despite some therapeutic advances, highlighting the need for a better understanding of its molecular etiology. The genomic landscape of OSCC is well-established and recent research has focused on miRNAs, which regulate gene expression and may be useful non-invasive biomarkers or therapeutic targets. A plethora of findings regarding miRNA expression have been generated, posing challenges for the interpretation and identification of disease-specific molecules. Hence, we opted to identify the most important regulatory miRNAs by bridging genetics and epigenetics, focusing on the key genes implicated in OSCC development. Based on published reports, we have developed custom panels of fifteen major oncogenes and five major tumor suppressor genes. Following a miRNA/target gene interaction analysis and a comprehensive study of the literature, we selected the miRNA molecules which target the majority of these panels that have been reported to be downregulated or upregulated in OSCC, respectively. As a result, miR-34a-5p, miR-155-5p, miR-124-3p, miR-1-3p, and miR-16-5p appeared to be the most OSCC-specific. Their expression patterns, verified targets, and the signaling pathways affected by their dysregulation in OSCC are thoroughly discussed.

摘要

口腔鳞状细胞癌(OSCC)是最常见的人类恶性肿瘤之一,尽管在某些治疗方面取得了进展,但预后仍然较差,这突显了需要更好地了解其分子病因。OSCC 的基因组图谱已经确立,最近的研究集中在 miRNA 上,miRNA 调节基因表达,可能是有用的非侵入性生物标志物或治疗靶点。已经产生了大量关于 miRNA 表达的发现,这给解释和鉴定疾病特异性分子带来了挑战。因此,我们选择通过桥接遗传学和表观遗传学来确定最重要的调节 miRNA,重点关注与 OSCC 发展相关的关键基因。基于已发表的报告,我们开发了十五种主要癌基因和五种主要肿瘤抑制基因的定制面板。在进行 miRNA/靶基因相互作用分析和对文献进行全面研究后,我们选择了针对这些报告中大多数分别下调或上调的面板的 miRNA 分子。结果表明,miR-34a-5p、miR-155-5p、miR-124-3p、miR-1-3p 和 miR-16-5p 似乎是最具 OSCC 特异性的。详细讨论了它们的表达模式、验证的靶标以及它们在 OSCC 中失调所影响的信号通路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ad5/10454361/cb0771dca03f/genes-14-01578-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验