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整合组织和血液 miRNA 表达谱可准确无创诊断乳腺癌:初步结果和未来临床意义。

Integrated Tissue and Blood miRNA Expression Profiles Identify Novel Biomarkers for Accurate Non-Invasive Diagnosis of Breast Cancer: Preliminary Results and Future Clinical Implications.

机构信息

College of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.

Department of Anatomy, Harbin Medical University, Harbin 150081, China.

出版信息

Genes (Basel). 2022 Oct 24;13(11):1931. doi: 10.3390/genes13111931.

Abstract

We aimed to identify miRNAs that were closely related to breast cancer (BRCA). By integrating several methods including significance analysis of microarrays, fold change, Pearson's correlation analysis, test, and receiver operating characteristic analysis, we developed a decision-tree-based scoring algorithm, called Optimized Scoring Mechanism for Primary Synergy MicroRNAs (O-PSM). Five synergy miRNAs (hsa-miR-139-5p, hsa-miR-331-3p, hsa-miR-342-5p, hsa-miR-486-5p, and hsa-miR-654-3p) were identified using O-PSM, which were used to distinguish normal samples from pathological ones, and showed good results in blood data and in multiple sets of tissue data. These five miRNAs showed accurate categorization efficiency in BRCA typing and staging and had better categorization efficiency than experimentally verified miRNAs. In the Protein-Protein Interaction (PPI) network, the target genes of hsa-miR-342-5p have the most regulatory relationships, which regulate carcinogenesis proliferation and metastasis by regulating Glycosaminoglycan biosynthesis and the Rap1 signaling pathway. Moreover, hsa-miR-342-5p showed potential clinical application in survival analysis. We also used O-PSM to generate an R package uploaded on github (SuFei-lab/OPSM accessed on 22 October 2021). We believe that miRNAs included in O-PSM could have clinical implications for diagnosis, prognostic stratification and treatment of BRCA, proposing potential significant biomarkers that could be utilized to design personalized treatment plans in BRCA patients in the future.

摘要

我们旨在鉴定与乳腺癌(BRCA)密切相关的 microRNAs。通过整合包括微阵列显著性分析、倍数变化、皮尔逊相关分析、t 检验和接收者操作特征分析在内的多种方法,我们开发了一种基于决策树的评分算法,称为原发性协同 microRNAs 的优化评分机制(O-PSM)。使用 O-PSM 鉴定了 5 个协同 microRNAs(hsa-miR-139-5p、hsa-miR-331-3p、hsa-miR-342-5p、hsa-miR-486-5p 和 hsa-miR-654-3p),可用于区分正常样本和病理样本,在血液数据和多组组织数据中均取得了良好的效果。这 5 个 microRNAs 在 BRCA 分型和分期中具有准确的分类效率,并且比经过实验验证的 microRNAs 具有更好的分类效率。在蛋白质-蛋白质相互作用(PPI)网络中,hsa-miR-342-5p 的靶基因具有最多的调控关系,通过调节糖胺聚糖生物合成和 Rap1 信号通路,调节致癌增殖和转移。此外,hsa-miR-342-5p 在生存分析中显示出潜在的临床应用价值。我们还使用 O-PSM 生成了一个在 github 上上传的 R 包(SuFei-lab/OPSM,访问时间为 2021 年 10 月 22 日)。我们相信,O-PSM 中包含的 microRNAs 可能对 BRCA 的诊断、预后分层和治疗具有临床意义,提出了潜在的有意义的生物标志物,可用于未来设计 BRCA 患者的个性化治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c56/9690091/c68d0e03da4b/genes-13-01931-g001.jpg

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