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Acta Biochim Biophys Sin (Shanghai). 2016 Aug;48(8):696-703. doi: 10.1093/abbs/gmw063. Epub 2016 Aug 18.
2
MicroRNA-194 promotes the growth, migration, and invasion of ovarian carcinoma cells by targeting protein tyrosine phosphatase nonreceptor type 12.微小RNA-194通过靶向非受体型12蛋白酪氨酸磷酸酶促进卵巢癌细胞的生长、迁移和侵袭。
Onco Targets Ther. 2016 Jul 15;9:4307-15. doi: 10.2147/OTT.S90976. eCollection 2016.
3
MicroRNA-130b functions as a tumor suppressor by regulating RUNX3 in epithelial ovarian cancer.微小RNA-130b通过调控上皮性卵巢癌中的RUNX3发挥肿瘤抑制作用。
Gene. 2016 Jul 15;586(1):48-55. doi: 10.1016/j.gene.2016.04.001. Epub 2016 Apr 2.
4
MicroRNA-9 suppresses cell migration and invasion through downregulation of TM4SF1 in colorectal cancer.微小RNA-9通过下调结直肠癌中的TM4SF1抑制细胞迁移和侵袭。
Int J Oncol. 2016 May;48(5):2135-43. doi: 10.3892/ijo.2016.3430. Epub 2016 Mar 9.
5
MicroRNA-203 suppresses gastric cancer growth by targeting PIBF1/Akt signaling.微小RNA-203通过靶向PIBF1/Akt信号通路抑制胃癌生长。
J Exp Clin Cancer Res. 2016 Mar 15;35:47. doi: 10.1186/s13046-016-0323-1.
6
Subpathway Analysis based on Signaling-Pathway Impact Analysis of Signaling Pathway.基于信号通路的信号通路影响分析的子通路分析
PLoS One. 2015 Jul 24;10(7):e0132813. doi: 10.1371/journal.pone.0132813. eCollection 2015.
7
MiR-133a is downregulated in non-small cell lung cancer: a study of clinical significance.MiR-133a在非小细胞肺癌中表达下调:临床意义研究
Eur J Med Res. 2015 Apr 23;20(1):50. doi: 10.1186/s40001-015-0139-z.
8
miR-218 inhibits the invasion and migration of colon cancer cells by targeting the PI3K/Akt/mTOR signaling pathway.微小RNA-218通过靶向PI3K/Akt/mTOR信号通路抑制结肠癌细胞的侵袭和迁移。
Int J Mol Med. 2015 May;35(5):1301-8. doi: 10.3892/ijmm.2015.2126. Epub 2015 Mar 6.
9
MicroRNA let-7b suppresses human gastric cancer malignancy by targeting ING1.微小 RNA let-7b 通过靶向 ING1 抑制人胃癌恶性表型。
Cancer Gene Ther. 2015 Apr;22(3):122-9. doi: 10.1038/cgt.2014.75. Epub 2015 Jan 23.
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Let-7b inhibits cell proliferation, migration, and invasion through targeting Cthrc1 in gastric cancer.Let-7b通过靶向胃癌中的Cthrc1抑制细胞增殖、迁移和侵袭。
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基于子路径识别癌症相关 microRNAs。

Identifying cancer-related microRNAs based on subpathways.

机构信息

Institute of Computational Science and Technology, Guangzhou University, Guangzhou, People's Republic of China.

Department of Information Engineering, Wenzhou Vocational College of Science and Technology, Wenzhou, People's Republic of China.

出版信息

IET Syst Biol. 2018 Dec;12(6):273-278. doi: 10.1049/iet-syb.2018.5025.

DOI:10.1049/iet-syb.2018.5025
PMID:30472691
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8687160/
Abstract

MicroRNAs (miRNAs) are a class of small endogenous non-coding genes that play important roles in post-transcriptional regulation as well as other important biological processes. Accumulating evidence indicated that miRNAs were extensively involved in the pathology of cancer. However, determining which miRNAs are related to a specific cancer is problematic because one miRNA may target multiple genes and one gene may be targeted by multiple miRNAs. The authors proposed a new approach, named miR_SubPath, to identify cancer-associated miRNAs by three steps. The targeted genes were determined based on differentially expressed genes in significant dysfunctional subpathways. Then the candidate miRNAs were determined according to miRNA-genes associations. Finally, these candidate miRNAs were ranked based on their relations with some seed miRNAs in a functional similarity network. Results on real-world datasets showed that the proposed miR_SubPath method was more robust and could identify more cancer-related miRNAs than a prior approach, miR_Path, miR_Clust and Zhang's method.

摘要

微小 RNA(miRNAs)是一类小型内源性非编码基因,在转录后调控以及其他重要的生物学过程中发挥重要作用。越来越多的证据表明,miRNAs 广泛参与癌症的病理过程。然而,确定哪些 miRNAs 与特定的癌症有关是一个问题,因为一个 miRNA 可能靶向多个基因,一个基因可能被多个 miRNAs 靶向。作者提出了一种新的方法,名为 miR_SubPath,通过三个步骤来识别与癌症相关的 miRNAs。根据显著功能失调子路径中的差异表达基因来确定靶向基因。然后根据 miRNA-genes 关联来确定候选 miRNAs。最后,根据它们与功能相似网络中某些种子 miRNAs 的关系对这些候选 miRNAs 进行排序。在真实数据集上的结果表明,所提出的 miR_SubPath 方法比以前的方法 miR_Path、miR_Clust 和 Zhang 的方法更稳健,并且可以识别更多与癌症相关的 miRNAs。