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微小RNA-126通过靶向血管内皮生长因子A信使核糖核酸调控乳腺癌血管生成。

MiR-126 Modulates Angiogenesis in Breast Cancer by Targeting VEGF-A -mRNA.

作者信息

Alhasan Layla

机构信息

Department of Biology, College Education for Pure Sciences, Thi-Qar University, Nasiriya, Iraq. Email: :

出版信息

Asian Pac J Cancer Prev. 2019 Jan 25;20(1):193-197. doi: 10.31557/APJCP.2019.20.1.193.

Abstract

Background: Breast cancer is most serious reasons of women death around worldwide result in increasing its morbidity and mortality. MicroRNAs are considered as significant regulators of cancer biological processes. The main aim of this study is restoration of miR-126 could lead to modulate breast cell line and impairs their proliferation by targeting vascular endothelial growth factor gene (VEGF-A). Methods: Breast cancer cell line (MCF7) was transfected by miR-126 lipofectamine and negative miR control for 24 hr. Cytotoxic effects of miR-126 lipofectamine were determined by cell viability assay. Cell proliferation and cell cycle were quantitatively measured using PicoGreen assay and DAPI stain-flow cytometer analysis. For further investigation, Taq-Man real time PCR assay was performed to detect relative VEGF-A and miRNA-126 level. Results: MiR-126 was overexpressed in treated breast cancer cell (MCF7) compared with control cells. miR-126 expression has been associated –with a decrease in cell proliferation and arrested MCF7 cells at G1 phase. The study found that vascular endothelial growth factor is regulated by miR- 126. Hence, VEGF-A is considered as functional vital and direct target to miR-126 in breast cancer cell line (MCF7). Conclusions: This study provided that manipulated miR-126 level may suggest a novel therapeutic approach in breast cancer treatment. However, an animal models study is needed to address and prove predictive ability of miR-126 on breast cancer controlling.

摘要

背景

乳腺癌是全球女性死亡的最主要原因,其发病率和死亡率不断上升。微小RNA被认为是癌症生物学过程的重要调节因子。本研究的主要目的是通过靶向血管内皮生长因子基因(VEGF-A)来恢复miR-126,从而调节乳腺癌细胞系并抑制其增殖。方法:用miR-126脂质体转染乳腺癌细胞系(MCF7)和阴性miR对照24小时。通过细胞活力测定法确定miR-126脂质体的细胞毒性作用。使用PicoGreen测定法和DAPI染色-流式细胞仪分析定量测量细胞增殖和细胞周期。为了进一步研究,进行Taq-Man实时PCR测定以检测相对VEGF-A和miRNA-126水平。结果:与对照细胞相比,miR-126在处理后的乳腺癌细胞(MCF7)中过表达。miR-126的表达与细胞增殖的减少相关,并使MCF7细胞停滞在G1期。研究发现血管内皮生长因子受miR-126调节。因此,VEGF-A被认为是乳腺癌细胞系(MCF7)中miR-126的功能性重要直接靶点。结论:本研究表明,调控miR-126水平可能为乳腺癌治疗提供一种新的治疗方法。然而,需要进行动物模型研究来探讨和证明miR-126对乳腺癌控制的预测能力。

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