Gold Nanoparticle-Delivered miR-26a Restricts Growth and Invasion of Gastric Cancer Cells

Junhua Yu, Jianping Fan, Yujun Zhao, Hang-Qing Lu, J. Qian
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Abstract

This paper aims to estimate the effect of miR-26a delivered by gold nanoparticles (AuNPs) on gastric cancer (GC) cell growth and invasion. In vitro cultured GC cell strains SGC-7901 and MGC- 803 were processed for transfection of miR-26a-mimic, miR-NC, AuNP-ctrl, and AuNP-miR-26a groups. MTT, Transwell, and flow cytometry were employed to evaluate the groups’ impact on cell vitality, invasion, and apoptosis. Western blotting (WB) was used to quantify the levels of apoptosisrelated proteins. In addition, solid tumors in mice were monitored for any changes that occurred under treatment by each group. We observed that overexpressing miR-26a restricted the vitality and invasion, and promoted apoptosis of GC cells; this effect became more significant with the injection of AuNP-delivered miR-26a, which evidently suppressed the growth of tumors in vivo. We conclude that, miR-26a serves as a tumor suppressor gene (TSG) in GC, and its effectiveness may be enhanced through delivery by AuNPs.
金纳米颗粒递送miR-26a抑制胃癌细胞的生长和侵袭
本文旨在评估金纳米颗粒(gold nanoparticles, AuNPs)递送miR-26a对胃癌(gastric cancer, GC)细胞生长和侵袭的影响。体外培养的GC细胞株SGC-7901和MGC- 803分别转染miR-26a-mimic、miR-NC、AuNP-ctrl和AuNP-miR-26a组。采用MTT、Transwell和流式细胞术评估各组对细胞活力、侵袭和凋亡的影响。Western blotting (WB)检测细胞凋亡相关蛋白水平。此外,还监测各组小鼠实体瘤在治疗过程中发生的变化。我们观察到过表达miR-26a抑制GC细胞的活力和侵袭,促进GC细胞凋亡;注射aunp传递的miR-26a后,这种作用更加明显,在体内可以明显抑制肿瘤的生长。我们得出结论,miR-26a在GC中作为肿瘤抑制基因(TSG),其有效性可能通过aunp的递送而增强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nanoscience and Nanotechnology Letters
Nanoscience and Nanotechnology Letters Physical, Chemical & Earth Sciences-MATERIALS SCIENCE, MULTIDISCIPLINARY
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审稿时长
2.6 months
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