• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

增强的血浆miR-26a-5p通过靶向PTEN促进膀胱癌进展。

Enhanced plasma miR-26a-5p promotes the progression of bladder cancer via targeting PTEN.

作者信息

Wang Hui, Hu Zhao, Chen Li

机构信息

Department of Nephrology, Qilu Hospital, Shandong University, Jinan, Shandong 250014, P.R. China.

Department of Nephrology, The Fourth Hospital of Jinan City, Jinan, Shandong 250031, P.R. China.

出版信息

Oncol Lett. 2018 Oct;16(4):4223-4228. doi: 10.3892/ol.2018.9163. Epub 2018 Jul 17.

DOI:10.3892/ol.2018.9163
PMID:30197668
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6126335/
Abstract

The current study aimed to evaluate the expression and specific role of miR-26a-5p in the progression of bladder cancer (BC). Reverse transcription-quantitative polymerase chain reaction analysis was performed to evaluate the level of miR-26a-5p in BC cancer and healthy controls. The present data showed that plasma miR-26a-5p was significantly increased in BC patients. Furthermore, BC tissues exhibited greater levels of miR-26a-5p compared with adjacent non-neoplastic tissues-26a-5p. Compared with BC patients at Ta-T1 stage, the level of miR-26a-5p was significantly elevated in BC patients ≥T2. BC patients at G3 stage demonstrated a higher plasma miR-26a-5p level compared with those at G1/2 stage. Receiver operating characteristic (ROC) analysis indicated that miR-26a-5p could differentiate BC patients from controls. Additionally, Kaplan-Meier analysis demonstrated that plasma miR-26a-5p negatively correlated with survival of BC patients. Dual luciferase reporter assay indicated that miR-26a-5p significantly suppressed the relative luciferase activity of pmirGLO-PTEN-3'UTR compared with the control. In conclusion, the current study indicated novel data that the levels of plasma miR-26a-5p was significantly increased in BC patients. Furthermore, the present study suggested that determination of plasma miR-26a-5p level could help to distinguish BC patients from healthy controls via targeting PTEN.

摘要

本研究旨在评估miR-26a-5p在膀胱癌(BC)进展中的表达及特定作用。采用逆转录定量聚合酶链反应分析来评估BC患者和健康对照中miR-26a-5p的水平。目前的数据显示,BC患者血浆中的miR-26a-5p显著升高。此外,与相邻的非肿瘤组织相比,BC组织中miR-26a-5p的水平更高。与Ta-T1期的BC患者相比,≥T2期的BC患者中miR-26a-5p的水平显著升高。G3期的BC患者与G1/2期的患者相比,血浆miR-26a-5p水平更高。受试者工作特征(ROC)分析表明,miR-26a-5p可区分BC患者与对照。此外,Kaplan-Meier分析表明,血浆miR-26a-5p与BC患者的生存率呈负相关。双荧光素酶报告基因检测表明,与对照相比,miR-26a-5p显著抑制了pmirGLO-PTEN-3'UTR的相对荧光素酶活性。总之,本研究表明了新的数据,即BC患者血浆中miR-26a-5p的水平显著升高。此外,本研究表明,通过靶向PTEN,测定血浆miR-26a-5p水平有助于区分BC患者与健康对照。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c94b/6126335/21c0b5f62a51/ol-16-04-4223-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c94b/6126335/2e582a180569/ol-16-04-4223-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c94b/6126335/4b22e1902e81/ol-16-04-4223-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c94b/6126335/59b850fdbdc3/ol-16-04-4223-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c94b/6126335/21c0b5f62a51/ol-16-04-4223-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c94b/6126335/2e582a180569/ol-16-04-4223-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c94b/6126335/4b22e1902e81/ol-16-04-4223-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c94b/6126335/59b850fdbdc3/ol-16-04-4223-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c94b/6126335/21c0b5f62a51/ol-16-04-4223-g03.jpg

相似文献

1
Enhanced plasma miR-26a-5p promotes the progression of bladder cancer via targeting PTEN.增强的血浆miR-26a-5p通过靶向PTEN促进膀胱癌进展。
Oncol Lett. 2018 Oct;16(4):4223-4228. doi: 10.3892/ol.2018.9163. Epub 2018 Jul 17.
2
Enhanced plasma miR-142-5p promotes the progression of intrahepatic cholangiocarcinoma via targeting PTEN.增强的血浆miR-142-5p通过靶向PTEN促进肝内胆管癌进展。
Exp Ther Med. 2019 May;17(5):4190-4196. doi: 10.3892/etm.2019.7438. Epub 2019 Mar 26.
3
MiR-26a-5p enhances cells proliferation, invasion, and apoptosis resistance of fibroblast-like synoviocytes in rheumatoid arthritis by regulating PTEN/PI3K/AKT pathway.miR-26a-5p 通过调控 PTEN/PI3K/AKT 通路增强类风湿关节炎成纤维样滑膜细胞的增殖、侵袭和抗凋亡能力。
Biosci Rep. 2019 Jul 25;39(7). doi: 10.1042/BSR20182192. Print 2019 Jul 31.
4
Tumour-suppressive miRNA-26a-5p and miR-26b-5p inhibit cell aggressiveness by regulating PLOD2 in bladder cancer.肿瘤抑制性miRNA-26a-5p和miR-26b-5p通过调节膀胱癌中的PLOD2来抑制细胞侵袭性。
Br J Cancer. 2016 Jul 26;115(3):354-63. doi: 10.1038/bjc.2016.179. Epub 2016 Jun 16.
5
Sperm miR-26a-5p and its target PTEN transcripts content in men with unexplained infertility.不明原因不孕男性精液中 miR-26a-5p 及其靶基因 PTEN 转录本含量。
Andrology. 2020 Sep;8(5):1167-1173. doi: 10.1111/andr.12801. Epub 2020 Jun 5.
6
Tumor-suppressor microRNA-139-5p restrains bladder cancer cell line ECV-304 properties via targeting Connexin 43.抑癌 microRNA-139-5p 通过靶向连接蛋白 43 抑制膀胱癌细胞系 ECV-304 的特性。
Chin Med J (Engl). 2019 Oct 5;132(19):2354-2361. doi: 10.1097/CM9.0000000000000455.
7
Long non-coding RNA SNHG6 enhances cell proliferation, migration and invasion by regulating miR-26a-5p/MAPK6 in breast cancer.长链非编码 RNA SNHG6 通过调控 miR-26a-5p/MAPK6 促进乳腺癌细胞增殖、迁移和侵袭。
Biomed Pharmacother. 2019 Feb;110:294-301. doi: 10.1016/j.biopha.2018.11.016. Epub 2018 Dec 3.
8
Down-regulation of miR-26a-5p in hepatocellular carcinoma: A qRT-PCR and bioinformatics study.肝细胞癌中miR-26a-5p的下调:一项qRT-PCR和生物信息学研究。
Pathol Res Pract. 2017 Dec;213(12):1494-1509. doi: 10.1016/j.prp.2017.10.001. Epub 2017 Oct 10.
9
miR-26a-5p protects against myocardial ischemia/reperfusion injury by regulating the PTEN/PI3K/AKT signaling pathway.miR-26a-5p 通过调控 PTEN/PI3K/AKT 信号通路保护心肌缺血/再灌注损伤。
Braz J Med Biol Res. 2020 Jan 24;53(2):e9106. doi: 10.1590/1414-431X20199106. eCollection 2020.
10
MiR-182-5p Knockdown Targeting PTEN Inhibits Cell Proliferation and Invasion of Breast Cancer Cells.靶向PTEN的miR-182-5p敲低抑制乳腺癌细胞的增殖和侵袭
Yonsei Med J. 2019 Feb;60(2):148-157. doi: 10.3349/ymj.2019.60.2.148.

引用本文的文献

1
Computational Elucidation of Hub Genes and Pathways Correlated with the Development of 5-Fluorouracil Resistance in HCT 116 Colorectal Carcinoma Cell Line.HCT 116结肠癌细胞系中与5-氟尿嘧啶耐药性发展相关的枢纽基因和信号通路的计算解析
Biochem Genet. 2025 Jan 30. doi: 10.1007/s10528-025-11041-2.
2
Natural compounds as modulators of miRNAs: a new frontier in bladder cancer treatment.天然化合物作为微小RNA的调节剂:膀胱癌治疗的新前沿。
Med Oncol. 2025 Jan 30;42(3):56. doi: 10.1007/s12032-025-02613-8.
3
Olaparib Combined with DDR Inhibitors Effectively Prevents EMT and Affects miRNA Regulation in -Mutated Epithelial Ovarian Cancer Cell Lines.

本文引用的文献

1
Evaluation of MUC1 and P53 expressions in noninvasive papillary urothelial neoplasms of bladder, their relationship with tumor grade and role in the differential diagnosis.膀胱非侵袭性乳头状尿路上皮肿瘤中MUC1和P53表达的评估、它们与肿瘤分级的关系以及在鉴别诊断中的作用。
Indian J Pathol Microbiol. 2017 Oct-Dec;60(4):510-514. doi: 10.4103/IJPM.IJPM_204_16.
2
Identification of a three miRNA signature as a novel potential prognostic biomarker in patients with bladder cancer.鉴定三种微小RNA特征作为膀胱癌患者一种新型潜在预后生物标志物
Oncotarget. 2017 Nov 6;8(62):105553-105560. doi: 10.18632/oncotarget.22318. eCollection 2017 Dec 1.
3
奥拉帕利联合DDR抑制剂可有效预防上皮性卵巢癌细胞系中的EMT并影响miRNA调控。
Int J Mol Sci. 2025 Jan 15;26(2):693. doi: 10.3390/ijms26020693.
4
miR-26a is a Key Therapeutic Target with Enormous Potential in the Diagnosis and Prognosis of Human Disease.miR-26a 是人类疾病诊断和预后的关键治疗靶点,具有巨大的潜力。
Curr Med Chem. 2024;31(18):2550-2570. doi: 10.2174/0109298673271808231116075056.
5
Knockdown of Long Noncoding RNA LINC00240 Inhibits Esophageal Cancer Progression by Regulating miR-26a-5p.长链非编码 RNA LINC00240 的敲低通过调节 miR-26a-5p 抑制食管癌进展。
Contrast Media Mol Imaging. 2022 Oct 5;2022:1071627. doi: 10.1155/2022/1071627. eCollection 2022.
6
Investigation of miRNA expression profiles using cohort samples reveals potential early detectability of colorectal cancers by serum miR-26a-5p before clinical diagnosis.使用队列样本对miRNA表达谱进行研究,结果显示血清miR-26a-5p在临床诊断前对结直肠癌具有潜在的早期可检测性。
Oncol Lett. 2022 Mar;23(3):87. doi: 10.3892/ol.2022.13207. Epub 2022 Jan 21.
7
MicroRNAs and Heat Shock Proteins in Breast Cancer Biology.微小 RNA 与热休克蛋白在乳腺癌生物学中的作用
Methods Mol Biol. 2022;2257:293-310. doi: 10.1007/978-1-0716-1170-8_15.
8
Small-sized extracellular vesicles (EVs) derived from acute myeloid leukemia bone marrow mesenchymal stem cells transfer miR-26a-5p to promote acute myeloid leukemia cell proliferation, migration, and invasion.来自急性髓系白血病骨髓间充质干细胞的小细胞外囊泡(EVs)将 miR-26a-5p 转移至急性髓系白血病细胞,促进其增殖、迁移和侵袭。
Hum Cell. 2021 May;34(3):965-976. doi: 10.1007/s13577-021-00501-7. Epub 2021 Feb 23.
9
Lnc-GAN1 expression is associated with good survival and suppresses tumor progression by sponging mir-26a-5p to activate PTEN signaling in non-small cell lung cancer.Lnc-GAN1 表达与良好的生存相关,并通过海绵吸附 mir-26a-5p 来激活 PTEN 信号通路从而抑制非小细胞肺癌的肿瘤进展。
J Exp Clin Cancer Res. 2021 Jan 6;40(1):9. doi: 10.1186/s13046-020-01819-0.
10
Up-Regulation of miR-26a-5p Inhibits E2F7 to Regulate the Progression of Renal Carcinoma Cells.miR-26a-5p的上调通过抑制E2F7调控肾癌细胞的进展。
Cancer Manag Res. 2020 Nov 17;12:11723-11733. doi: 10.2147/CMAR.S271710. eCollection 2020.
Long non-coding RNA urothelial carcinoma-associated 1 as a tumor biomarker for the diagnosis of urinary bladder cancer.
长链非编码RNA尿路上皮癌相关1作为诊断膀胱癌的肿瘤生物标志物。
Tumour Biol. 2017 Jun;39(6):1010428317709990. doi: 10.1177/1010428317709990.
4
Combining Protein and miRNA Quantification for Bladder Cancer Analysis.联合蛋白质和 miRNA 定量分析用于膀胱癌研究。
ACS Appl Mater Interfaces. 2017 Jul 19;9(28):23420-23427. doi: 10.1021/acsami.7b05639. Epub 2017 Jul 6.
5
Mirna Expression in Bladder Cancer and Their Potential Role in Clinical Practice.微小RNA在膀胱癌中的表达及其在临床实践中的潜在作用。
Curr Drug Metab. 2017 Oct 16;18(8):712-722. doi: 10.2174/1389200218666170518164507.
6
miRNA-556-3p promotes human bladder cancer proliferation, migration and invasion by negatively regulating DAB2IP expression.miRNA-556-3p 通过负向调控 DAB2IP 表达促进人膀胱癌的增殖、迁移和侵袭。
Int J Oncol. 2017 Jun;50(6):2101-2112. doi: 10.3892/ijo.2017.3969. Epub 2017 Apr 20.
7
miR-26b enhances radiosensitivity of hepatocellular carcinoma cells by targeting EphA2.微小RNA-26b通过靶向EphA2增强肝癌细胞的放射敏感性。
Iran J Basic Med Sci. 2016 Aug;19(8):851-857.
8
Establishment and antitumor effects of dasatinib and PKI-587 in BD-138T, a patient-derived muscle invasive bladder cancer preclinical platform with concomitant EGFR amplification and PTEN deletion.达沙替尼和PKI-587在BD-138T中的建立及抗肿瘤作用,BD-138T是一个源自患者的伴有表皮生长因子受体(EGFR)扩增和第10号染色体缺失的磷酸酶及张力蛋白同源物(PTEN)缺失的肌层浸润性膀胱癌临床前平台。
Oncotarget. 2016 Aug 9;7(32):51626-51639. doi: 10.18632/oncotarget.10539.
9
miR-130b, an onco-miRNA in bladder cancer, is directly regulated by NF-κB and sustains NF-κB activation by decreasing Cylindromatosis expression.miR-130b是膀胱癌中的一种致癌微小RNA,它直接受核因子κB调控,并通过降低圆柱瘤蛋白的表达来维持核因子κB的激活。
Oncotarget. 2016 Jul 26;7(30):48547-48561. doi: 10.18632/oncotarget.10423.
10
The miR-130 family promotes cell migration and invasion in bladder cancer through FAK and Akt phosphorylation by regulating PTEN.miR-130家族通过调节PTEN使FAK和Akt磷酸化,从而促进膀胱癌细胞的迁移和侵袭。
Sci Rep. 2016 Feb 3;6:20574. doi: 10.1038/srep20574.