期刊文献+
共找到3篇文章
< 1 >
每页显示 20 50 100
肺癌细胞外泌体来源的miR-718通过靶向PTEN诱导血管新生
1
作者 付婷 李芳 +2 位作者 潘大燕 夏园园 张秋园 《中国临床药理学与治疗学》 CAS CSCD 2023年第6期624-632,共9页
目的:探究肺癌细胞外泌体(exosome,exo)对血管新生的影响及机制。方法:提取人肺上皮细胞HFL-1和人肺癌细胞A549、H522、H460细胞分泌的外泌体,记为HFL-1 exo、A549 exo、H522 exo、H460 exo,将上述外泌体以及等体积的PBS缓冲液与人脐静... 目的:探究肺癌细胞外泌体(exosome,exo)对血管新生的影响及机制。方法:提取人肺上皮细胞HFL-1和人肺癌细胞A549、H522、H460细胞分泌的外泌体,记为HFL-1 exo、A549 exo、H522 exo、H460 exo,将上述外泌体以及等体积的PBS缓冲液与人脐静脉内皮细胞(HUVEC)共孵育,记为HFL-1 exo组、A549 exo组、H522 exo组、H460 exo组和PBS组,PBS组作为对照组。HUVEC转染PTEN siRNA和Negative control,记为si-PTEN组和si-NC组。提取转染miR-NC、miR-718 mimic、miR-718 inhibitor的A549细胞所分泌的外泌体,记为A549/miR-NC exo、A549/miR-718 mimic exo、A549/miR-718 inhibitor exo,将上述外泌体与HUVEC细胞共孵育,记为A549/miR-NC exo组、A549/miR-718 mimic exo组、A549/miR-718 inhibitor exo组,HUVEC细胞与A549/miR-718 mimic exo孵育后转染PTEN过表达质粒,记为A549/miR-718 mimic exo+PTEN组。实时荧光定量聚合酶链反应(qRTPCR)检测各组细胞及外泌体miR-718的表达;Transwell小室法和小管形成实验检测各组细胞的迁移能力和小管形成情况;Western blot检测PTEN蛋白的表达。结果:本文所提取的HFL-1 exo、A549 exo、H522 exo、H460 exo均符合外泌体的结构特征;与PBS组比较,A549 exo、H522 exo、H460 exo组HUVEC细胞迁移数和小管形成数显著升高(P均<0.05)。与HFL-1细胞比较,A549、H522、H460细胞中miR-718表达显著升高(P均<0.05)。与HFL-1 exo比较,A549 exo、H522 exo、H460 exo中miR-718表达显著升高(P均<0.05),并且miR-718可靶向调控PTEN的表达。相比于si-NC组,si-PTEN组HUVEC细胞小管形成和细胞迁移数显著升高(P均<0.05)。相比于A549/miRNC exo组,A549/miR-718 mimic exo组细胞迁移和小管形成数显著增加(P均<0.05),A549/miR-718 inhibitor exo组细胞迁移和小管形成数显著减少(P均<0.05);相比于A549/miR-NC exo组,A549/miR-718 mimic exo+PTEN组细胞迁移和小管形成数显著升高(P均<0.05)。结论:肺癌细胞外泌体miR-718能够通过靶向抑制PTEN的表达而促进血管生成。 展开更多
关键词 肺癌 外泌体 mir-718 PTEN 血管新生
下载PDF
lncRNA TOPORS-AS1靶向miR-718对胃癌细胞增殖、迁移和凋亡调控作用研究
2
作者 邱实 曹佳懿 余雅靖 《河北医药》 CAS 2022年第19期2920-2924,共5页
目的探讨lncRNA TOPORS-AS1靶向miR-718对胃癌细胞增殖、迁移和凋亡的调控作用。方法RT-qPCR分析TOPORS-AS1和miR-718在胃癌组织、细胞系中的表达。将pcDNA、pcDNA-TOPORS-AS1、anti-miR-NC、anti-miR-718、pcDNA-TOPORS-AS1+miR-NC、pc... 目的探讨lncRNA TOPORS-AS1靶向miR-718对胃癌细胞增殖、迁移和凋亡的调控作用。方法RT-qPCR分析TOPORS-AS1和miR-718在胃癌组织、细胞系中的表达。将pcDNA、pcDNA-TOPORS-AS1、anti-miR-NC、anti-miR-718、pcDNA-TOPORS-AS1+miR-NC、pcDNA-TOPORS-AS1+miR-718分别转染HGC-27细胞,通过CCK-8和克隆形成实验评估细胞增殖;流式细胞术检测细胞凋亡;Transwell法分析细胞迁移。TOPORS-AS1对miR-718的靶向调控作用通过RT-qPCR和双荧光素酶报告实验验证。结果TOPORS-AS1在胃癌组织、细胞系中表达显著升高(P<0.05),miR-718的表达显著降低(P<0.05)。过表达TOPORS-AS1后HGC-27细胞克隆形成数、迁移数、miR-718表达显著降低(P<0.05),抑制率、凋亡率显著升高(P<0.05)。抑制miR-718表达后HGC-27细胞克隆形成数、迁移数显著降低(P<0.05),抑制率、凋亡率显著升高(P<0.05)。miR-718是TOPORS-AS1的直接靶点。过表达miR-718显著减弱TOPORS-AS1过表达对HGC-27细胞增殖、迁移和凋亡的影响(P<0.05)。结论TOPORS-AS1负调控miR-718抑制胃癌细胞增殖、迁移并促进凋亡。 展开更多
关键词 胃癌 TOPORS-AS1 mir-718 增殖 迁移 凋亡
下载PDF
Involvement of micro RNA-718,a new regulator of EGR3,in regulation of malignant phenotype of HCC cells 被引量:3
3
作者 Zhong-dong WANG Fan-yong QU +3 位作者 Yuan-yuan CHEN Zhang-shen RAN Hai-yan LIU Hai-dong ZHANG 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2017年第1期27-36,共10页
Objective: Hepatocellular carcinoma (HCC) is still one of the most common death-related malignancies worldwide. Because the way onset and progression are hidden most, HCC diagnoses are made at an advanced stage, wh... Objective: Hepatocellular carcinoma (HCC) is still one of the most common death-related malignancies worldwide. Because the way onset and progression are hidden most, HCC diagnoses are made at an advanced stage, when they are unsuitable for surgical resection. MicroRNAs are a class of small non-coding RNAs, participating in many aspects of cancers. In this study, we tried to establish the role of micreRNA-718 (miR-718) in the malignant phenotype of HCC cells and its possible role in HCC diagnosis. Methods: Here we first used a methylthiazolyldiphenyl- tetrazolium bromide (MTT) assay, Transwell migration and invasion assays, and colony formation assay to evaluate the impact of miR-718 on the malignant phenotypes of HCC cells. Then, we used bioinformatic methods to predict the target gene of miR-718 and used green fluorescence protein (GFP) reporter assay, Western blot, and quantitative real-time polymerase chain reaction (qRT-PCR) to validate the regulation relationship. Finally, we determined the role of the target gene in the HCC phenotype. Results: We found that the expression of miR-718 was significantly reduced in various HCC cell lines and HCC tissues. Re-expression of miR-718 significantly reduced the cellular viability and colony formation ability as well as inhibited the migration and invasion abilities of HCC cell lines. Early growth response protein 3 (EGR3) is a direct target of miR-718 and is negatively regulated by miR-718. EGR3 could increase the via- bility and proliferation of HCC cells, and promot the migration and invasion of HCC cells. Conclusions: miR-718 acts as a tumor suppressive microRNA in HCC via regulating the expression of EGR3, which may provide a new diagnostic 07) found that overexpreget for HCC. 展开更多
关键词 mir-718 MicroRNA Early growth response protein 3 (EGR3) Hepatocellular carcinoma (HCC) Malignant phenotype
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部