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Tanshinone IIA May Inhibit Gastric Cancer via Affecting the Intestinal Microbiome
BACKGROUND: Gastric cancer (GC) belongs to a type of the most deadly cancer in the world, and the incidence rate of GC will increase in the coming decades. Tanshinone IIA (Tan IIA) is an active component that separated from Danshen. Tan IIA may also exert its therapeutic effects in disease with inte...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9529444/ https://www.ncbi.nlm.nih.gov/pubmed/36199775 http://dx.doi.org/10.1155/2022/6960304 |
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author | Lu, Fenggang Zhang, Yi Song, Pinghui Xu, Yu Wu, Zhongkun Wang, Qinyu Shen, Naiying |
author_facet | Lu, Fenggang Zhang, Yi Song, Pinghui Xu, Yu Wu, Zhongkun Wang, Qinyu Shen, Naiying |
author_sort | Lu, Fenggang |
collection | PubMed |
description | BACKGROUND: Gastric cancer (GC) belongs to a type of the most deadly cancer in the world, and the incidence rate of GC will increase in the coming decades. Tanshinone IIA (Tan IIA) is an active component that separated from Danshen. Tan IIA may also exert its therapeutic effects in disease with intestinal dysbacteriosis, at least partially, via regulating the intestinal microbiome. Nevertheless, it is obscure whether Tanshinone IIA affects the intestinal dysbacteriosis and plays antitumor roles. This research was designed to explore Tanshinone IIA potential on the intestinal dysbacteriosis of GC xenograft mice. METHODS: Mouse xenograft GC tumor models were built and treated by Tan IIA. The tumor growth as well as microbiome in the intestinal were compared. Western blot was used to detect the phosphorylation of the NF-κB and expressions of the downstream cytokines IL-6 and IL-1β. RESULTS: Microbiome in the intestinal was changed in xenograft tumor mice in comparison with the control mice. What is more, Tan IIA could influence the microbiome in the intestinal of the tumor mice. Tan IIA hinders the growth of xenograft tumor and change the microbiome in the intestinal, but intestinal dysbacteriosis condition partially blocked Tan IIA-stimulated antitumor effects. In addition, intestinal dysbacteriosis abrogated Tan IIA-stimulated decrease in the NF-κB signaling in xenograft tumor mice. CONCLUSIONS: Tanshinone IIA may inhibit GC tumor growth via affecting the intestinal microbiome through regulating the NF-κB signaling. |
format | Online Article Text |
id | pubmed-9529444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-95294442022-10-04 Tanshinone IIA May Inhibit Gastric Cancer via Affecting the Intestinal Microbiome Lu, Fenggang Zhang, Yi Song, Pinghui Xu, Yu Wu, Zhongkun Wang, Qinyu Shen, Naiying Comput Math Methods Med Research Article BACKGROUND: Gastric cancer (GC) belongs to a type of the most deadly cancer in the world, and the incidence rate of GC will increase in the coming decades. Tanshinone IIA (Tan IIA) is an active component that separated from Danshen. Tan IIA may also exert its therapeutic effects in disease with intestinal dysbacteriosis, at least partially, via regulating the intestinal microbiome. Nevertheless, it is obscure whether Tanshinone IIA affects the intestinal dysbacteriosis and plays antitumor roles. This research was designed to explore Tanshinone IIA potential on the intestinal dysbacteriosis of GC xenograft mice. METHODS: Mouse xenograft GC tumor models were built and treated by Tan IIA. The tumor growth as well as microbiome in the intestinal were compared. Western blot was used to detect the phosphorylation of the NF-κB and expressions of the downstream cytokines IL-6 and IL-1β. RESULTS: Microbiome in the intestinal was changed in xenograft tumor mice in comparison with the control mice. What is more, Tan IIA could influence the microbiome in the intestinal of the tumor mice. Tan IIA hinders the growth of xenograft tumor and change the microbiome in the intestinal, but intestinal dysbacteriosis condition partially blocked Tan IIA-stimulated antitumor effects. In addition, intestinal dysbacteriosis abrogated Tan IIA-stimulated decrease in the NF-κB signaling in xenograft tumor mice. CONCLUSIONS: Tanshinone IIA may inhibit GC tumor growth via affecting the intestinal microbiome through regulating the NF-κB signaling. Hindawi 2022-09-26 /pmc/articles/PMC9529444/ /pubmed/36199775 http://dx.doi.org/10.1155/2022/6960304 Text en Copyright © 2022 Fenggang Lu et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Lu, Fenggang Zhang, Yi Song, Pinghui Xu, Yu Wu, Zhongkun Wang, Qinyu Shen, Naiying Tanshinone IIA May Inhibit Gastric Cancer via Affecting the Intestinal Microbiome |
title | Tanshinone IIA May Inhibit Gastric Cancer via Affecting the Intestinal Microbiome |
title_full | Tanshinone IIA May Inhibit Gastric Cancer via Affecting the Intestinal Microbiome |
title_fullStr | Tanshinone IIA May Inhibit Gastric Cancer via Affecting the Intestinal Microbiome |
title_full_unstemmed | Tanshinone IIA May Inhibit Gastric Cancer via Affecting the Intestinal Microbiome |
title_short | Tanshinone IIA May Inhibit Gastric Cancer via Affecting the Intestinal Microbiome |
title_sort | tanshinone iia may inhibit gastric cancer via affecting the intestinal microbiome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9529444/ https://www.ncbi.nlm.nih.gov/pubmed/36199775 http://dx.doi.org/10.1155/2022/6960304 |
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