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Honeysuckle-derived microRNA2911 inhibits tumor growth by targeting TGF-β1

BACKGROUND: Honeysuckle is a time‐honored herb with anticancer activity in traditional Chinese medicine. Recently, accumulating reports are suggesting that the microRNAs in this medicinal plant not only play a physiological role in their original system, but also can be transmitted to another specie...

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Autores principales: Liu, Chunyan, Xu, Mengzhen, Yan, Luocheng, Wang, Yulian, Zhou, Zhen, Wang, Shaocong, Sun, Yajie, Zhang, Junfeng, Dong, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8244210/
https://www.ncbi.nlm.nih.gov/pubmed/34187513
http://dx.doi.org/10.1186/s13020-021-00453-y
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author Liu, Chunyan
Xu, Mengzhen
Yan, Luocheng
Wang, Yulian
Zhou, Zhen
Wang, Shaocong
Sun, Yajie
Zhang, Junfeng
Dong, Lei
author_facet Liu, Chunyan
Xu, Mengzhen
Yan, Luocheng
Wang, Yulian
Zhou, Zhen
Wang, Shaocong
Sun, Yajie
Zhang, Junfeng
Dong, Lei
author_sort Liu, Chunyan
collection PubMed
description BACKGROUND: Honeysuckle is a time‐honored herb with anticancer activity in traditional Chinese medicine. Recently, accumulating reports are suggesting that the microRNAs in this medicinal plant not only play a physiological role in their original system, but also can be transmitted to another species as potential therapeutic components. In the numerous bioactive investigations, the anti-tumor effects of these microRNAs in the magical herb are rarely studied, especially the special miR2911, a honeysuckle-encoded atypical microRNA, with high stability during the boiling process and unique biological activity to target TGF-β1 mRNA. METHODS: Luciferase assay was conducted to test the ability of miR2911 to target TGF-β1 mRNA. ELISA was performed to determine the expression level of TGF-β1 of mouse colorectal adenocarcinoma CT26 cells when treated with miR2911 and tumor tissue in Sidt1(+/+) and Sidt1(−/−) mice. qRT-PCR was performed to examine the level of expression of miR2911. Tumor-bearing wild and nude mice were employed to evaluate the anti-tumor effect of honeysuckle and miR2911 in vivo. Tumor tissue necrosis was observed by H&E staining. Besides, the infiltration of T lymphocytes across solid tumors was tested by immunostaining staining. RESULTS: Our results showed that honeysuckle slowed the development of colon cancer down. Further research showed that miR2911 could bind strongly to TGF-β1 mRNA and down-regulate the expression of TGF-β1 and had a high stability under boiling and acid condition. Moreover, SIDT1 mediated dietary miR2911 inter-species absorption. And we found that miR2911 had a similar anticancer effect as honeysuckle. Mechanistically, miR2911 reversed the tumor-promoting effect of TGF-β1 by an increase of T lymphocytes infiltration, resulting in slowing the colon cancer process in immunocompetent mice. Consistent with this inference, the anti-tumor effect of miR2911 was revealed to be abolished in T cell immune deficiency mice. CONCLUSION: Taken together, honeysuckle-derived miR2911 showed an anti-tumor effect in colon cancer through targeting TGF-β1 mRNA. The down-regulation of TGF-β1 promoted T lymphocytes infiltration, and accordingly impeded the colon tumor development. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13020-021-00453-y.
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spelling pubmed-82442102021-06-30 Honeysuckle-derived microRNA2911 inhibits tumor growth by targeting TGF-β1 Liu, Chunyan Xu, Mengzhen Yan, Luocheng Wang, Yulian Zhou, Zhen Wang, Shaocong Sun, Yajie Zhang, Junfeng Dong, Lei Chin Med Research BACKGROUND: Honeysuckle is a time‐honored herb with anticancer activity in traditional Chinese medicine. Recently, accumulating reports are suggesting that the microRNAs in this medicinal plant not only play a physiological role in their original system, but also can be transmitted to another species as potential therapeutic components. In the numerous bioactive investigations, the anti-tumor effects of these microRNAs in the magical herb are rarely studied, especially the special miR2911, a honeysuckle-encoded atypical microRNA, with high stability during the boiling process and unique biological activity to target TGF-β1 mRNA. METHODS: Luciferase assay was conducted to test the ability of miR2911 to target TGF-β1 mRNA. ELISA was performed to determine the expression level of TGF-β1 of mouse colorectal adenocarcinoma CT26 cells when treated with miR2911 and tumor tissue in Sidt1(+/+) and Sidt1(−/−) mice. qRT-PCR was performed to examine the level of expression of miR2911. Tumor-bearing wild and nude mice were employed to evaluate the anti-tumor effect of honeysuckle and miR2911 in vivo. Tumor tissue necrosis was observed by H&E staining. Besides, the infiltration of T lymphocytes across solid tumors was tested by immunostaining staining. RESULTS: Our results showed that honeysuckle slowed the development of colon cancer down. Further research showed that miR2911 could bind strongly to TGF-β1 mRNA and down-regulate the expression of TGF-β1 and had a high stability under boiling and acid condition. Moreover, SIDT1 mediated dietary miR2911 inter-species absorption. And we found that miR2911 had a similar anticancer effect as honeysuckle. Mechanistically, miR2911 reversed the tumor-promoting effect of TGF-β1 by an increase of T lymphocytes infiltration, resulting in slowing the colon cancer process in immunocompetent mice. Consistent with this inference, the anti-tumor effect of miR2911 was revealed to be abolished in T cell immune deficiency mice. CONCLUSION: Taken together, honeysuckle-derived miR2911 showed an anti-tumor effect in colon cancer through targeting TGF-β1 mRNA. The down-regulation of TGF-β1 promoted T lymphocytes infiltration, and accordingly impeded the colon tumor development. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13020-021-00453-y. BioMed Central 2021-06-29 /pmc/articles/PMC8244210/ /pubmed/34187513 http://dx.doi.org/10.1186/s13020-021-00453-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Liu, Chunyan
Xu, Mengzhen
Yan, Luocheng
Wang, Yulian
Zhou, Zhen
Wang, Shaocong
Sun, Yajie
Zhang, Junfeng
Dong, Lei
Honeysuckle-derived microRNA2911 inhibits tumor growth by targeting TGF-β1
title Honeysuckle-derived microRNA2911 inhibits tumor growth by targeting TGF-β1
title_full Honeysuckle-derived microRNA2911 inhibits tumor growth by targeting TGF-β1
title_fullStr Honeysuckle-derived microRNA2911 inhibits tumor growth by targeting TGF-β1
title_full_unstemmed Honeysuckle-derived microRNA2911 inhibits tumor growth by targeting TGF-β1
title_short Honeysuckle-derived microRNA2911 inhibits tumor growth by targeting TGF-β1
title_sort honeysuckle-derived microrna2911 inhibits tumor growth by targeting tgf-β1
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8244210/
https://www.ncbi.nlm.nih.gov/pubmed/34187513
http://dx.doi.org/10.1186/s13020-021-00453-y
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