Exosomes derived from microRNA-129-5p-modified tumor cells selectively enhanced suppressive effect in malignant behaviors of homologous colon cancer cells

Exosome-encapsulated microRNAs (miRNAs) are novel diagnostic and predictive markers in colon cancer. Hence, the study of serum exosomal miRNAs in patients with colon cancer may help its diagnosis and treatment. PKH26-labeled exosomal uptake analysis identified whether exosomes transfer miRNA-129-5p...

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Autores principales: Yong Ji, Jianxiang Ji, Hongming Yin, Xu Chen, Pengcheng Zhao, Huahu Lu, Taowu Wang
Formato: article
Lenguaje:EN
Publicado: Taylor & Francis Group 2021
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Acceso en línea:https://doaj.org/article/a11d824343964ef1ab2de14ff87ed8e4
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spelling oai:doaj.org-article:a11d824343964ef1ab2de14ff87ed8e42021-11-17T14:21:59ZExosomes derived from microRNA-129-5p-modified tumor cells selectively enhanced suppressive effect in malignant behaviors of homologous colon cancer cells2165-59792165-598710.1080/21655979.2021.2004981https://doaj.org/article/a11d824343964ef1ab2de14ff87ed8e42021-11-01T00:00:00Zhttp://dx.doi.org/10.1080/21655979.2021.2004981https://doaj.org/toc/2165-5979https://doaj.org/toc/2165-5987Exosome-encapsulated microRNAs (miRNAs) are novel diagnostic and predictive markers in colon cancer. Hence, the study of serum exosomal miRNAs in patients with colon cancer may help its diagnosis and treatment. PKH26-labeled exosomal uptake analysis identified whether exosomes transfer miRNA-129-5p to target cells. Transmission electron microscopy and dynamic light scattering analysis were applied to determine exosome morphology and size distribution. The Cell Counting Kit-8, wound healing assay and Transwell assays were used to detect cell proliferation, migration, and invasion after treatment with engineered exosomes. Moreover, the western blotting was used to quantify the expression of proteins involved in cell apoptosis. In our study, hepatocellular liver carcinoma, cervical cancer and colon cancer cells were selected as the target cells of miRNA-129-5p exosomes. Exosomes containing miRNA-129-5p were found to be significantly more easily absorbed by colon cancer cells, presenting a stronger inhibitory effect on colon cancer cell proliferation. MiRNA-129-5p exosomes induced apoptosis in colon cancer cells while inhibiting their proliferation, migration, and invasion. In conclusion, exosomes derived from miRNA-129-5p-modified tumor cells selectively inhibited colon cancer progression, shedding new insights to therapeutic efficacy of this cancer.Yong JiJianxiang JiHongming YinXu ChenPengcheng ZhaoHuahu LuTaowu WangTaylor & Francis Grouparticlehomologous colon cancerexosomesmirna-129-5pgene expressionmolecular mechanismBiotechnologyTP248.13-248.65ENBioengineered, Vol 0, Iss 0 (2021)
institution DOAJ
collection DOAJ
language EN
topic homologous colon cancer
exosomes
mirna-129-5p
gene expression
molecular mechanism
Biotechnology
TP248.13-248.65
spellingShingle homologous colon cancer
exosomes
mirna-129-5p
gene expression
molecular mechanism
Biotechnology
TP248.13-248.65
Yong Ji
Jianxiang Ji
Hongming Yin
Xu Chen
Pengcheng Zhao
Huahu Lu
Taowu Wang
Exosomes derived from microRNA-129-5p-modified tumor cells selectively enhanced suppressive effect in malignant behaviors of homologous colon cancer cells
description Exosome-encapsulated microRNAs (miRNAs) are novel diagnostic and predictive markers in colon cancer. Hence, the study of serum exosomal miRNAs in patients with colon cancer may help its diagnosis and treatment. PKH26-labeled exosomal uptake analysis identified whether exosomes transfer miRNA-129-5p to target cells. Transmission electron microscopy and dynamic light scattering analysis were applied to determine exosome morphology and size distribution. The Cell Counting Kit-8, wound healing assay and Transwell assays were used to detect cell proliferation, migration, and invasion after treatment with engineered exosomes. Moreover, the western blotting was used to quantify the expression of proteins involved in cell apoptosis. In our study, hepatocellular liver carcinoma, cervical cancer and colon cancer cells were selected as the target cells of miRNA-129-5p exosomes. Exosomes containing miRNA-129-5p were found to be significantly more easily absorbed by colon cancer cells, presenting a stronger inhibitory effect on colon cancer cell proliferation. MiRNA-129-5p exosomes induced apoptosis in colon cancer cells while inhibiting their proliferation, migration, and invasion. In conclusion, exosomes derived from miRNA-129-5p-modified tumor cells selectively inhibited colon cancer progression, shedding new insights to therapeutic efficacy of this cancer.
format article
author Yong Ji
Jianxiang Ji
Hongming Yin
Xu Chen
Pengcheng Zhao
Huahu Lu
Taowu Wang
author_facet Yong Ji
Jianxiang Ji
Hongming Yin
Xu Chen
Pengcheng Zhao
Huahu Lu
Taowu Wang
author_sort Yong Ji
title Exosomes derived from microRNA-129-5p-modified tumor cells selectively enhanced suppressive effect in malignant behaviors of homologous colon cancer cells
title_short Exosomes derived from microRNA-129-5p-modified tumor cells selectively enhanced suppressive effect in malignant behaviors of homologous colon cancer cells
title_full Exosomes derived from microRNA-129-5p-modified tumor cells selectively enhanced suppressive effect in malignant behaviors of homologous colon cancer cells
title_fullStr Exosomes derived from microRNA-129-5p-modified tumor cells selectively enhanced suppressive effect in malignant behaviors of homologous colon cancer cells
title_full_unstemmed Exosomes derived from microRNA-129-5p-modified tumor cells selectively enhanced suppressive effect in malignant behaviors of homologous colon cancer cells
title_sort exosomes derived from microrna-129-5p-modified tumor cells selectively enhanced suppressive effect in malignant behaviors of homologous colon cancer cells
publisher Taylor & Francis Group
publishDate 2021
url https://doaj.org/article/a11d824343964ef1ab2de14ff87ed8e4
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AT jianxiangji exosomesderivedfrommicrorna1295pmodifiedtumorcellsselectivelyenhancedsuppressiveeffectinmalignantbehaviorsofhomologouscoloncancercells
AT hongmingyin exosomesderivedfrommicrorna1295pmodifiedtumorcellsselectivelyenhancedsuppressiveeffectinmalignantbehaviorsofhomologouscoloncancercells
AT xuchen exosomesderivedfrommicrorna1295pmodifiedtumorcellsselectivelyenhancedsuppressiveeffectinmalignantbehaviorsofhomologouscoloncancercells
AT pengchengzhao exosomesderivedfrommicrorna1295pmodifiedtumorcellsselectivelyenhancedsuppressiveeffectinmalignantbehaviorsofhomologouscoloncancercells
AT huahulu exosomesderivedfrommicrorna1295pmodifiedtumorcellsselectivelyenhancedsuppressiveeffectinmalignantbehaviorsofhomologouscoloncancercells
AT taowuwang exosomesderivedfrommicrorna1295pmodifiedtumorcellsselectivelyenhancedsuppressiveeffectinmalignantbehaviorsofhomologouscoloncancercells
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