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鉴定预测乳腺癌分期的 miRNA 特征。

Identifying a miRNA signature for predicting the stage of breast cancer.

机构信息

Institute of Bioinformatics and Systems Biology, National Chiao Tung University, Hsinchu, Taiwan.

Department of Biological Science and Technology, National Chiao Tung University, Hsinchu, Taiwan.

出版信息

Sci Rep. 2018 Oct 31;8(1):16138. doi: 10.1038/s41598-018-34604-3.

DOI:10.1038/s41598-018-34604-3
PMID:30382159
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6208346/
Abstract

Breast cancer is a heterogeneous disease and one of the most common cancers among women. Recently, microRNAs (miRNAs) have been used as biomarkers due to their effective role in cancer diagnosis. This study proposes a support vector machine (SVM)-based classifier SVM-BRC to categorize patients with breast cancer into early and advanced stages. SVM-BRC uses an optimal feature selection method, inheritable bi-objective combinatorial genetic algorithm, to identify a miRNA signature which is a small set of informative miRNAs while maximizing prediction accuracy. MiRNA expression profiles of a 386-patient cohort of breast cancer were retrieved from The Cancer Genome Atlas. SVM-BRC identified 34 of 503 miRNAs as a signature and achieved a 10-fold cross-validation mean accuracy, sensitivity, specificity, and Matthews correlation coefficient of 80.38%, 0.79, 0.81, and 0.60, respectively. Functional enrichment of the 10 highest ranked miRNAs was analysed in terms of Kyoto Encyclopedia of Genes and Genomes and Gene Ontology annotations. Kaplan-Meier survival analysis of the highest ranked miRNAs revealed that four miRNAs, hsa-miR-503, hsa-miR-1307, hsa-miR-212 and hsa-miR-592, were significantly associated with the prognosis of patients with breast cancer.

摘要

乳腺癌是一种异质性疾病,也是女性中最常见的癌症之一。最近,由于 microRNAs(miRNAs)在癌症诊断中的有效作用,它们已被用作生物标志物。本研究提出了一种基于支持向量机(SVM)的分类器 SVM-BRC,用于将乳腺癌患者分为早期和晚期。SVM-BRC 使用一种最优特征选择方法,可遗传的双目标组合遗传算法,来识别 miRNA 特征,这是一组信息量较小的有意义的 miRNAs,同时最大限度地提高预测准确性。从癌症基因组图谱中检索了 386 名乳腺癌患者的 miRNA 表达谱。SVM-BRC 确定了 34 个 miRNA 作为特征,在 10 倍交叉验证中平均准确率、灵敏度、特异性和 Matthews 相关系数分别为 80.38%、0.79、0.81 和 0.60。根据京都基因与基因组百科全书和基因本体论注释分析了排名前 10 的 miRNA 的功能富集。排名前 10 的 miRNA 的 Kaplan-Meier 生存分析表明,hsa-miR-503、hsa-miR-1307、hsa-miR-212 和 hsa-miR-592 这四个 miRNA 与乳腺癌患者的预后显著相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcec/6208346/a4f950ff149d/41598_2018_34604_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcec/6208346/35d3168c0654/41598_2018_34604_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcec/6208346/cf2e78fb7b17/41598_2018_34604_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcec/6208346/73dbd88dcf1d/41598_2018_34604_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcec/6208346/3c8c08f623f8/41598_2018_34604_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcec/6208346/a4f950ff149d/41598_2018_34604_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcec/6208346/35d3168c0654/41598_2018_34604_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcec/6208346/cf2e78fb7b17/41598_2018_34604_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcec/6208346/73dbd88dcf1d/41598_2018_34604_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcec/6208346/3c8c08f623f8/41598_2018_34604_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcec/6208346/a4f950ff149d/41598_2018_34604_Fig5_HTML.jpg

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1
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2
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Gene. 2018 Nov 30;677:111-118. doi: 10.1016/j.gene.2018.07.057. Epub 2018 Jul 25.
3
Predicting miRNA-disease association based on inductive matrix completion.
Med Oncol. 2024 Dec 17;42(1):30. doi: 10.1007/s12032-024-02579-z.
4
MiR-592 Attenuates Tamoxifen Resistance in Breast Cancer Through PIK3CA-Mediated PI3K/AKT/mTOR Signaling Pathway.微小RNA-592通过PIK3CA介导的PI3K/AKT/mTOR信号通路减轻乳腺癌中的他莫昔芬耐药性。
Appl Biochem Biotechnol. 2025 Mar;197(3):2051-2065. doi: 10.1007/s12010-024-05123-x. Epub 2024 Dec 11.
5
Exploring prognostic implications of miRNA signatures and telomere maintenance genes in kidney cancer.探索微小RNA特征和端粒维持基因在肾癌中的预后意义。
Mol Ther Oncol. 2024 Sep 10;32(4):200874. doi: 10.1016/j.omton.2024.200874. eCollection 2024 Dec 19.
6
MicroRNA-1307-3p contributes to breast cancer progression through PRM2.miR-1307-3p 通过 PRM2 促进乳腺癌的进展。
Thorac Cancer. 2024 Nov;15(32):2298-2308. doi: 10.1111/1759-7714.15460. Epub 2024 Oct 9.
7
A deep drug prediction framework for viral infectious diseases using an optimizer-based ensemble of convolutional neural network: COVID-19 as a case study.一种基于优化器的卷积神经网络集成的病毒性传染病深度药物预测框架:以COVID-19为例
Mol Divers. 2025 Jun;29(3):2473-2487. doi: 10.1007/s11030-024-11003-7. Epub 2024 Oct 9.
8
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Commun Biol. 2024 Jul 13;7(1):859. doi: 10.1038/s42003-024-06555-1.
9
Identification of Gene Expression in Different Stages of Breast Cancer with Machine Learning.利用机器学习识别乳腺癌不同阶段的基因表达
Cancers (Basel). 2024 May 14;16(10):1864. doi: 10.3390/cancers16101864.
10
Ensemble-based classification using microRNA expression identifies a breast cancer patient subgroup with an ultralow long-term risk of metastases.基于微小RNA表达的集成分类法可识别出具有超低长期转移风险的乳腺癌患者亚组。
Cancer Med. 2024 May;13(9):e7089. doi: 10.1002/cam4.7089.
基于归纳矩阵补全的 miRNA-疾病关联预测。
Bioinformatics. 2018 Dec 15;34(24):4256-4265. doi: 10.1093/bioinformatics/bty503.
4
BNPMDA: Bipartite Network Projection for MiRNA-Disease Association prediction.BNPMDA:基于二分网络投影的 miRNA-疾病关联预测方法。
Bioinformatics. 2018 Sep 15;34(18):3178-3186. doi: 10.1093/bioinformatics/bty333.
5
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Sci Rep. 2018 Jan 17;8(1):951. doi: 10.1038/s41598-017-18648-5.
6
EGBMMDA: Extreme Gradient Boosting Machine for MiRNA-Disease Association prediction.EGBMMDA:用于 miRNA-疾病关联预测的极端梯度提升机。
Cell Death Dis. 2018 Jan 5;9(1):3. doi: 10.1038/s41419-017-0003-x.
7
LRSSLMDA: Laplacian Regularized Sparse Subspace Learning for MiRNA-Disease Association prediction.LRSSLMDA:用于miRNA-疾病关联预测的拉普拉斯正则化稀疏子空间学习
PLoS Comput Biol. 2017 Dec 18;13(12):e1005912. doi: 10.1371/journal.pcbi.1005912. eCollection 2017 Dec.
8
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Cell Physiol Biochem. 2017;44(5):1785-1795. doi: 10.1159/000485785. Epub 2017 Dec 6.
9
MiR-361-5p inhibits glycolytic metabolism, proliferation and invasion of breast cancer by targeting FGFR1 and MMP-1.miR-361-5p 通过靶向 FGFR1 和 MMP-1 抑制乳腺癌的糖酵解代谢、增殖和侵袭。
J Exp Clin Cancer Res. 2017 Nov 13;36(1):158. doi: 10.1186/s13046-017-0630-1.
10
Suppressive role of miR-592 in breast cancer by repressing TGF-β2.miR-592 通过抑制 TGF-β2 在乳腺癌中发挥抑制作用。
Oncol Rep. 2017 Dec;38(6):3447-3454. doi: 10.3892/or.2017.6029. Epub 2017 Oct 12.