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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Taylor & Francis Group
2021
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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) |
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homologous colon cancer exosomes mirna-129-5p gene expression molecular mechanism Biotechnology TP248.13-248.65 |
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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 |
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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 |
work_keys_str_mv |
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1718425433052020736 |