Preparation, characterisation, and in vitro cancer‐suppression function of RNA nanoparticles carrying miR‐301b‐3p Inhibitor

Abstract Background Multidrug resistance is the biggest barrier on the way to chemotherapy for lung adenocarcinoma (LUAD). For some LUAD patients with cisplatin (DDP) resistance and poor prognoses, the authors put forward RNA nanoparticles (NPs) carrying miR‐301b‐3p Inhibitor. Methods The NPs were c...

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Main Authors: Junjie Zhao, Niu Niu, Fan Yang, Haitao Liu, Weibo Qi
Format: Article
Language:English
Published: Wiley 2023-05-01
Series:IET Nanobiotechnology
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Online Access:https://doi.org/10.1049/nbt2.12120
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author Junjie Zhao
Niu Niu
Fan Yang
Haitao Liu
Weibo Qi
author_facet Junjie Zhao
Niu Niu
Fan Yang
Haitao Liu
Weibo Qi
author_sort Junjie Zhao
collection DOAJ
description Abstract Background Multidrug resistance is the biggest barrier on the way to chemotherapy for lung adenocarcinoma (LUAD). For some LUAD patients with cisplatin (DDP) resistance and poor prognoses, the authors put forward RNA nanoparticles (NPs) carrying miR‐301b‐3p Inhibitor. Methods The NPs were composed of miR‐301b‐3p, A549 aptamer (A549apt), and Cyanine 5 in a bottom‐up manner with a 3‐way‐junction (3WJ) structure. Diameter, assembly process, and morphology of NPs were observed by Dynamic Light Scattering, Native‐Polyacrylamide Gel Electrophoresis, and Atomic Force Microscopy. Cell internalisation, toxicity, proliferation, migration, invasion, and apoptosis were assayed by confocal laser scanning microscope, CCK8, colony formation assay, Transwell, western blot, and flow cytometry. Results 3WJ‐apt‐miR was evenly distributed, with diameter of 19.61 ± 0.49 nm and triangular branching structures. The accurate delivery of this NP in vivo was ensured by A549 aptamer featuring specific targeting, with smaller side effects than traditional chemotherapy. Such nanomaterials were effectively internalized by cancer cells, with normal cell activity intact. Cancer cell proliferation, invasion, and migration were suppressed, and DDP sensitivity was enhanced, causing DNA damage and facilitating apoptosis of DDP‐resistant cells. Conclusion Based on RNA self‐assembling, the authors researched the effect of miRNA on DDP sensitivity in LUAD regarding gene regulation. 3WJ‐apt‐miR paves the way for clinical tumour therapy.
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spelling doaj-art-efe2f951c4014b5a8c82937f143cec002025-02-03T06:45:07ZengWileyIET Nanobiotechnology1751-87411751-875X2023-05-0117322423310.1049/nbt2.12120Preparation, characterisation, and in vitro cancer‐suppression function of RNA nanoparticles carrying miR‐301b‐3p InhibitorJunjie Zhao0Niu Niu1Fan Yang2Haitao Liu3Weibo Qi4Department of Cardiothoracic Surgery Affiliated Hospital of Jiaxing University (the First Hospital of Jiaxing) Jiaxing Zhejiang ChinaDepartment of Cardiothoracic Surgery Affiliated Hospital of Jiaxing University (the First Hospital of Jiaxing) Jiaxing Zhejiang ChinaDepartment of Cardiothoracic Surgery Affiliated Hospital of Jiaxing University (the First Hospital of Jiaxing) Jiaxing Zhejiang ChinaDepartment of Cardiothoracic Surgery Affiliated Hospital of Jiaxing University (the First Hospital of Jiaxing) Jiaxing Zhejiang ChinaDepartment of Cardiothoracic Surgery Affiliated Hospital of Jiaxing University (the First Hospital of Jiaxing) Jiaxing Zhejiang ChinaAbstract Background Multidrug resistance is the biggest barrier on the way to chemotherapy for lung adenocarcinoma (LUAD). For some LUAD patients with cisplatin (DDP) resistance and poor prognoses, the authors put forward RNA nanoparticles (NPs) carrying miR‐301b‐3p Inhibitor. Methods The NPs were composed of miR‐301b‐3p, A549 aptamer (A549apt), and Cyanine 5 in a bottom‐up manner with a 3‐way‐junction (3WJ) structure. Diameter, assembly process, and morphology of NPs were observed by Dynamic Light Scattering, Native‐Polyacrylamide Gel Electrophoresis, and Atomic Force Microscopy. Cell internalisation, toxicity, proliferation, migration, invasion, and apoptosis were assayed by confocal laser scanning microscope, CCK8, colony formation assay, Transwell, western blot, and flow cytometry. Results 3WJ‐apt‐miR was evenly distributed, with diameter of 19.61 ± 0.49 nm and triangular branching structures. The accurate delivery of this NP in vivo was ensured by A549 aptamer featuring specific targeting, with smaller side effects than traditional chemotherapy. Such nanomaterials were effectively internalized by cancer cells, with normal cell activity intact. Cancer cell proliferation, invasion, and migration were suppressed, and DDP sensitivity was enhanced, causing DNA damage and facilitating apoptosis of DDP‐resistant cells. Conclusion Based on RNA self‐assembling, the authors researched the effect of miRNA on DDP sensitivity in LUAD regarding gene regulation. 3WJ‐apt‐miR paves the way for clinical tumour therapy.https://doi.org/10.1049/nbt2.12120nanomedicinetumours
spellingShingle Junjie Zhao
Niu Niu
Fan Yang
Haitao Liu
Weibo Qi
Preparation, characterisation, and in vitro cancer‐suppression function of RNA nanoparticles carrying miR‐301b‐3p Inhibitor
IET Nanobiotechnology
nanomedicine
tumours
title Preparation, characterisation, and in vitro cancer‐suppression function of RNA nanoparticles carrying miR‐301b‐3p Inhibitor
title_full Preparation, characterisation, and in vitro cancer‐suppression function of RNA nanoparticles carrying miR‐301b‐3p Inhibitor
title_fullStr Preparation, characterisation, and in vitro cancer‐suppression function of RNA nanoparticles carrying miR‐301b‐3p Inhibitor
title_full_unstemmed Preparation, characterisation, and in vitro cancer‐suppression function of RNA nanoparticles carrying miR‐301b‐3p Inhibitor
title_short Preparation, characterisation, and in vitro cancer‐suppression function of RNA nanoparticles carrying miR‐301b‐3p Inhibitor
title_sort preparation characterisation and in vitro cancer suppression function of rna nanoparticles carrying mir 301b 3p inhibitor
topic nanomedicine
tumours
url https://doi.org/10.1049/nbt2.12120
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