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Dual Strands of Pre-miR-149 Inhibit Cancer Cell Migration and Invasion through Targeting FOXM1 in Renal Cell Carcinoma.miR-149 的双链通过靶向肾细胞癌中的 FOXM1 抑制癌细胞迁移和侵袭。
Int J Mol Sci. 2017 Sep 13;18(9):1969. doi: 10.3390/ijms18091969.
2
miRNAs and ovarian cancer: An overview.miRNAs 与卵巢癌:概述。
J Cell Physiol. 2018 May;233(5):3846-3854. doi: 10.1002/jcp.26095. Epub 2017 Aug 25.
3
MicroRNA-mediated drug resistance in ovarian cancer.微小 RNA 介导的卵巢癌耐药性。
J Cell Physiol. 2019 Apr;234(4):3180-3191. doi: 10.1002/jcp.26060. Epub 2017 Jul 14.
4
The emerging roles and therapeutic potential of exosomes in epithelial ovarian cancer.外泌体在上皮性卵巢癌中的新兴作用及治疗潜力
Mol Cancer. 2017 May 15;16(1):92. doi: 10.1186/s12943-017-0659-y.
5
MicroRNAs driving invasion and metastasis in ovarian cancer: Opportunities for translational medicine (Review).驱动卵巢癌侵袭和转移的微小RNA:转化医学的机遇(综述)
Int J Oncol. 2017 May;50(5):1461-1476. doi: 10.3892/ijo.2017.3948. Epub 2017 Apr 4.
6
Dealing with microscopic peritoneal metastases of epithelial ovarian cancer. A surgical challenge.处理上皮性卵巢癌的微小腹膜转移灶:一项外科挑战。
Surg Oncol. 2017 Mar;26(1):46-52. doi: 10.1016/j.suronc.2017.01.001. Epub 2017 Jan 6.
7
Malignant extracellular vesicles carrying MMP1 mRNA facilitate peritoneal dissemination in ovarian cancer.携带 MMP1 mRNA 的恶性细胞外囊泡促进卵巢癌腹膜扩散。
Nat Commun. 2017 Mar 6;8:14470. doi: 10.1038/ncomms14470.
8
Potent effects of dioscin against pancreatic cancer via miR-149-3P-mediated inhibition of the Akt1 signalling pathway.薯蓣皂苷通过miR-149-3P介导的Akt1信号通路抑制对胰腺癌具有显著作用。
Br J Pharmacol. 2017 Apr;174(7):553-568. doi: 10.1111/bph.13718. Epub 2017 Feb 14.
9
A network-biology perspective of microRNA function and dysfunction in cancer.癌症中 microRNA 功能与失调的网络生物学视角
Nat Rev Genet. 2016 Dec;17(12):719-732. doi: 10.1038/nrg.2016.134. Epub 2016 Oct 31.
10
Exosomes Promote Ovarian Cancer Cell Invasion through Transfer of CD44 to Peritoneal Mesothelial Cells.外泌体通过将 CD44 转移至腹膜间皮细胞促进卵巢癌细胞侵袭。
Mol Cancer Res. 2017 Jan;15(1):78-92. doi: 10.1158/1541-7786.MCR-16-0191. Epub 2016 Oct 6.

通过高通量测序对卵巢癌患者腹膜外泌体微小RNA进行特征分析。

Characterizing the landscape of peritoneal exosomal microRNAs in patients with ovarian cancer by high-throughput sequencing.

作者信息

Li Yuankun, Liu Cuihua, Liao Yumei, Wang Wuliang, Hu Bin, Lu Xiaoqin, Cui Jinquan

机构信息

Department of Gynecology, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450000, P.R. China.

Department of Gynecology, Zhengzhou First People's Hospital, Zhengzhou, Henan 450000, P.R. China.

出版信息

Oncol Lett. 2019 Jan;17(1):539-547. doi: 10.3892/ol.2018.9558. Epub 2018 Oct 9.

DOI:10.3892/ol.2018.9558
PMID:30655799
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6313212/
Abstract

In the present study, differentially expressed microRNAs (miRNAs) in peritoneal exosomes that were isolated from 10 patients with epithelial ovarian cancer (EOC) with metastasis in the abdominal cavity and 10 participants without cancer (NC) were identified. These differentially expressed miRNAs that were revealed by next-generation sequencing were categorized by Gene Ontology enrichment and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis of their target genes. Notably, two miRNAs that were associated with EOC-miR-149-3p and miR-222-5p-were identified. There were significant differences in expression of miR-149-3p and miR-222-5p between EOC and NC samples, and the effect of the expression level of the two miRNAs on the patient survival was identified using publicly available data from The Cancer Genome Atlas. There is an association between these two miRNAs and EOC, that was further verified by reverse transcription-quantitative polymerase chain reaction in peritoneal exosomes from 10 patients with EOC and NC participants. These results indicated that miR-149-3p and miR-222-5p might be novel biomarkers for evaluating the prognosis of patients with EOC and that these two miRNAs might have potential therapeutic values.

摘要

在本研究中,我们鉴定了从10例伴有腹腔转移的上皮性卵巢癌(EOC)患者及10例无癌参与者(NC)中分离出的腹膜外泌体中差异表达的微小RNA(miRNA)。通过下一代测序揭示的这些差异表达的miRNA,根据其靶基因的基因本体富集分析和京都基因与基因组百科全书通路富集分析进行分类。值得注意的是,鉴定出了两种与EOC相关的miRNA——miR-149-3p和miR-222-5p。EOC样本与NC样本中miR-149-3p和miR-222-5p的表达存在显著差异,并利用来自癌症基因组图谱的公开数据确定了这两种miRNA的表达水平对患者生存的影响。通过对10例EOC患者和NC参与者的腹膜外泌体进行逆转录定量聚合酶链反应,进一步验证了这两种miRNA与EOC之间的关联。这些结果表明,miR-149-3p和miR-222-5p可能是评估EOC患者预后的新型生物标志物,并且这两种miRNA可能具有潜在的治疗价值。