• 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

miR-205 在肾细胞癌中的表达及其与临床病理特征和预后的关系。

Expression of miR-205 in renal cell carcinoma and its association with clinicopathological features and prognosis.

机构信息

Department of Nephrology, Weifang People's Hospital, Weifang, Shandong Province, China.

出版信息

Eur Rev Med Pharmacol Sci. 2018 Feb;22(3):662-670. doi: 10.26355/eurrev_201802_14291.

DOI:10.26355/eurrev_201802_14291
PMID:29461593
Abstract

OBJECTIVE

The aim of the present study was to examine the expression of miR-205 in renal cell carcinoma (RCC) tissue and carcinoma cells; also, we aimed to determine the association of miR-205 expression with the clinicopathological features and prognosis of RCC, and to explore the mechanism of miR-205.

PATIENTS AND METHODS

Carcinoma tissue and adjacent normal tissue were collected from 60 patients with RCC, and the expression of miR-205 was determined by semi-quantitative PCR, followed by correlation analysis of miR-205 with clinicopathological features and prognosis. Subsequently, the human RCC line, ACHN, was transfected with miR-205, and the effect of miR-205 overexpression on the growth of RCC was examined by MTT assay. Moreover, the effect of miR-205 on the migration of colon cancer cells was studied by transwell assay. Additionally, immunohistochemistry and Western blot were used to investigate the epithelial-mesenchymal transition in renal cancer tissue.

RESULTS

The expression of miR-205 was downregulated in RCC tissue compared with adjacent non-cancerous tissue (p < 0.01). The expression of miR-205 was closely related to the infiltration and recurrence of tumors (p < 0.01), but was not correlated with a pathological grade or clinical stage (p > 0.05). We also found that overexpression of miR-205 in RCC significantly inhibited the growth of cancer cells (p < 0.01) and significantly reduced the migration ability (p < 0.01). The epithelial-mesenchymal transition occurs in RCC, and miR-205 might inhibit cell proliferation and migration by blocking the epithelial-mesenchymal transition.

CONCLUSIONS

The expression of miR-205 is low in RCC, and may play an important role throughout the progression of RCC. Further study of miR-205 may promote the development of a novel therapeutic approach for the treatment of RCC.

摘要

目的

本研究旨在检测 miR-205 在肾细胞癌(RCC)组织和癌细胞中的表达,并探讨 miR-205 的表达与 RCC 临床病理特征和预后的相关性,同时研究 miR-205 的作用机制。

方法

收集 60 例 RCC 患者的癌组织及癌旁正常组织,采用半定量 PCR 检测 miR-205 的表达情况,对 miR-205 与临床病理特征和预后的相关性进行分析。随后,将 miR-205 转染入人 RCC 细胞系 ACHN,通过 MTT 实验检测 miR-205 过表达对 RCC 生长的影响。通过 Transwell 实验研究 miR-205 对结肠癌细胞迁移的影响。采用免疫组化和 Western blot 检测肾癌细胞上皮间质转化。

结果

与癌旁非癌组织相比,RCC 组织中 miR-205 的表达下调(p<0.01)。miR-205 的表达与肿瘤浸润和复发密切相关(p<0.01),但与病理分级或临床分期无关(p>0.05)。我们还发现,在 RCC 中过表达 miR-205 可显著抑制癌细胞的生长(p<0.01)和迁移能力(p<0.01)。RCC 中发生上皮间质转化,miR-205 可能通过阻断上皮间质转化抑制细胞增殖和迁移。

结论

miR-205 在 RCC 中表达下调,可能在 RCC 的发生发展中发挥重要作用。对 miR-205 的进一步研究可能促进开发治疗 RCC 的新方法。

相似文献

1
Expression of miR-205 in renal cell carcinoma and its association with clinicopathological features and prognosis.miR-205 在肾细胞癌中的表达及其与临床病理特征和预后的关系。
Eur Rev Med Pharmacol Sci. 2018 Feb;22(3):662-670. doi: 10.26355/eurrev_201802_14291.
2
Epithelial-mesenchymal transition-related microRNA-200s regulate molecular targets and pathways in renal cell carcinoma.上皮-间充质转化相关 microRNA-200s 调控肾细胞癌中的分子靶标和通路。
J Hum Genet. 2013 Aug;58(8):508-16. doi: 10.1038/jhg.2013.31. Epub 2013 May 2.
3
MicroRNA-509-3p inhibits cancer cell proliferation and migration by targeting the mitogen-activated protein kinase kinase kinase 8 oncogene in renal cell carcinoma.微小RNA-509-3p通过靶向肾细胞癌中的丝裂原活化蛋白激酶激酶激酶8癌基因来抑制癌细胞的增殖和迁移。
Mol Med Rep. 2015 Jul;12(1):1535-43. doi: 10.3892/mmr.2015.3498. Epub 2015 Mar 17.
4
MiR-429 is linked to metastasis and poor prognosis in renal cell carcinoma by affecting epithelial-mesenchymal transition.MiR-429通过影响上皮-间质转化与肾细胞癌的转移及不良预后相关。
Tumour Biol. 2016 Nov;37(11):14653-14658. doi: 10.1007/s13277-016-5310-9. Epub 2016 Sep 12.
5
miR-566 functions as an oncogene and a potential biomarker for prognosis in renal cell carcinoma.miR-566 在肾细胞癌中作为癌基因和潜在的预后生物标志物发挥作用。
Biomed Pharmacother. 2018 Jun;102:718-727. doi: 10.1016/j.biopha.2018.03.072. Epub 2018 Apr 5.
6
microRNA-200c modulates the epithelial-to-mesenchymal transition in human renal cell carcinoma metastasis.miRNA-200c 调控人肾透明细胞癌转移中的上皮间质转化。
Oncol Rep. 2013 Aug;30(2):643-50. doi: 10.3892/or.2013.2530. Epub 2013 Jun 7.
7
Downregulation of microRNA-15a suppresses the proliferation and invasion of renal cell carcinoma via direct targeting of eIF4E.微小RNA-15a的下调通过直接靶向真核翻译起始因子4E抑制肾细胞癌的增殖和侵袭。
Oncol Rep. 2017 Oct;38(4):1995-2002. doi: 10.3892/or.2017.5901. Epub 2017 Aug 11.
8
Effect of MicroRNA-218 on the viability, apoptosis and invasion of renal cell carcinoma cells under hypoxia by targeted downregulation of CXCR7 expression.靶向下调 CXCR7 表达对低氧环境下肾癌细胞活力、凋亡和侵袭的影响。
Biomed Pharmacother. 2016 May;80:213-219. doi: 10.1016/j.biopha.2016.03.011. Epub 2016 Mar 28.
9
Uc.416 + A promotes epithelial-to-mesenchymal transition through miR-153 in renal cell carcinoma.Uc.416 + A通过miR-153促进肾细胞癌上皮-间质转化。
BMC Cancer. 2018 Oct 4;18(1):952. doi: 10.1186/s12885-018-4863-y.
10
miR-134 functions as a tumor suppressor in cell proliferation and epithelial-to-mesenchymal Transition by targeting KRAS in renal cell carcinoma cells.微小RNA-134通过靶向肾癌细胞中的KRAS,在细胞增殖和上皮-间质转化过程中发挥肿瘤抑制作用。
DNA Cell Biol. 2015 Jun;34(6):429-36. doi: 10.1089/dna.2014.2629. Epub 2015 Mar 26.

引用本文的文献

1
Tanshinone IIA Improves Ventricular Remodeling following Cardiac Infarction by Regulating miR-205-3p.丹参酮 IIA 通过调控 miR-205-3p 改善心肌梗死后心室重构。
Dis Markers. 2021 Nov 29;2021:8740831. doi: 10.1155/2021/8740831. eCollection 2021.
2
Evaluation of Diagnostic Potential of Epigenetically Deregulated MiRNAs in Epithelial Ovarian Cancer.表观遗传失调的微小RNA在上皮性卵巢癌中的诊断潜力评估
Front Oncol. 2021 Oct 7;11:681872. doi: 10.3389/fonc.2021.681872. eCollection 2021.
3
MicroRNAs in Body Fluids: A More Promising Biomarker for Clear Cell Renal Cell Carcinoma.
体液中的微小RNA:肾透明细胞癌更具前景的生物标志物
Cancer Manag Res. 2021 Oct 5;13:7663-7675. doi: 10.2147/CMAR.S330881. eCollection 2021.
4
The Pathogenic Role of PI3K/AKT Pathway in Cancer Onset and Drug Resistance: An Updated Review.PI3K/AKT信号通路在癌症发生和耐药中的致病作用:最新综述
Cancers (Basel). 2021 Aug 5;13(16):3949. doi: 10.3390/cancers13163949.
5
miR-205: A Potential Biomedicine for Cancer Therapy.miR-205:癌症治疗的潜在生物医学。
Cells. 2020 Aug 25;9(9):1957. doi: 10.3390/cells9091957.
6
The lncRNA SNHG5-mediated miR-205-5p downregulation contributes to the progression of clear cell renal cell carcinoma by targeting ZEB1.长链非编码 RNA SNHG5 通过靶向 ZEB1 下调 miR-205-5p 促进肾透明细胞癌的进展。
Cancer Med. 2020 Jun;9(12):4251-4264. doi: 10.1002/cam4.3052. Epub 2020 Apr 12.
7
MiR-1208 Increases the Sensitivity to Cisplatin by Targeting TBCK in Renal Cancer Cells.miR-1208 通过靶向 TBCK 增加肾癌细胞对顺铂的敏感性。
Int J Mol Sci. 2019 Jul 19;20(14):3540. doi: 10.3390/ijms20143540.
8
Molecular Mechanisms in Clear Cell Renal Cell Carcinoma: Role of miRNAs and Hypermethylated miRNA Genes in Crucial Oncogenic Pathways and Processes.透明细胞肾细胞癌的分子机制:微小RNA及微小RNA基因高甲基化在关键致癌途径和过程中的作用
Front Genet. 2019 Apr 24;10:320. doi: 10.3389/fgene.2019.00320. eCollection 2019.