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Nicaraven Attenuates Postoperative Systemic Inflammatory Responses-Induced Tumor Metastasis
BACKGROUND: Inflammation has been demonstrated to promote cancer metastasis. Due to the well-known systemic inflammatory responses (SIR) after major surgery, it is critical to investigate and attenuate SIR-induced tumor metastasis of cancer patients suffering surgical procedures. METHODS: C57BL/6 mi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7060163/ https://www.ncbi.nlm.nih.gov/pubmed/31873930 http://dx.doi.org/10.1245/s10434-019-08076-2 |
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author | Zhang, Xu Moriwaki, Takahito Kawabata, Tsuyoshi Goto, Shinji Liu, Ke-Xiang Guo, Chang-Ying Li, Tao-Sheng |
author_facet | Zhang, Xu Moriwaki, Takahito Kawabata, Tsuyoshi Goto, Shinji Liu, Ke-Xiang Guo, Chang-Ying Li, Tao-Sheng |
author_sort | Zhang, Xu |
collection | PubMed |
description | BACKGROUND: Inflammation has been demonstrated to promote cancer metastasis. Due to the well-known systemic inflammatory responses (SIR) after major surgery, it is critical to investigate and attenuate SIR-induced tumor metastasis of cancer patients suffering surgical procedures. METHODS: C57BL/6 mice were intravenously injected with Lewis lung cancer cells at 6, 24, and 72 h after the induction of intestinal ischemia/reperfusion (I/R) injury. We found that the number of tumor nodules significantly increased in lungs of mice injected with cancer cells at 6 h but not at 24 and 72 h after I/R injury. The administration of nicaraven 30 min before and 24 h after I/R injury effectively attenuated the enhanced tumor metastasis to lungs. Protein array showed the increase of various cytokines in plasma of mice at 6 h after I/R injury, but many of them were attenuated by the administration of nicaraven. Immunostaining indicated the increase of Ly6g-, CD206-, and CD11c-positive inflammatory cells in the lungs, but it was also attenuated by nicaraven administration. CONCLUSIONS: Postoperative SIR-induced tumor metastasis have been clearly evidenced in our experimental model, and the administration of nicaraven may ameliorate the SIR-induced tumor metastasis by suppressing inflammatory responses. |
format | Online Article Text |
id | pubmed-7060163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-70601632020-03-23 Nicaraven Attenuates Postoperative Systemic Inflammatory Responses-Induced Tumor Metastasis Zhang, Xu Moriwaki, Takahito Kawabata, Tsuyoshi Goto, Shinji Liu, Ke-Xiang Guo, Chang-Ying Li, Tao-Sheng Ann Surg Oncol Translational Research and Biomarkers BACKGROUND: Inflammation has been demonstrated to promote cancer metastasis. Due to the well-known systemic inflammatory responses (SIR) after major surgery, it is critical to investigate and attenuate SIR-induced tumor metastasis of cancer patients suffering surgical procedures. METHODS: C57BL/6 mice were intravenously injected with Lewis lung cancer cells at 6, 24, and 72 h after the induction of intestinal ischemia/reperfusion (I/R) injury. We found that the number of tumor nodules significantly increased in lungs of mice injected with cancer cells at 6 h but not at 24 and 72 h after I/R injury. The administration of nicaraven 30 min before and 24 h after I/R injury effectively attenuated the enhanced tumor metastasis to lungs. Protein array showed the increase of various cytokines in plasma of mice at 6 h after I/R injury, but many of them were attenuated by the administration of nicaraven. Immunostaining indicated the increase of Ly6g-, CD206-, and CD11c-positive inflammatory cells in the lungs, but it was also attenuated by nicaraven administration. CONCLUSIONS: Postoperative SIR-induced tumor metastasis have been clearly evidenced in our experimental model, and the administration of nicaraven may ameliorate the SIR-induced tumor metastasis by suppressing inflammatory responses. Springer International Publishing 2019-12-23 2020 /pmc/articles/PMC7060163/ /pubmed/31873930 http://dx.doi.org/10.1245/s10434-019-08076-2 Text en © The Author(s) 2019 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/. |
spellingShingle | Translational Research and Biomarkers Zhang, Xu Moriwaki, Takahito Kawabata, Tsuyoshi Goto, Shinji Liu, Ke-Xiang Guo, Chang-Ying Li, Tao-Sheng Nicaraven Attenuates Postoperative Systemic Inflammatory Responses-Induced Tumor Metastasis |
title | Nicaraven Attenuates Postoperative Systemic Inflammatory Responses-Induced Tumor Metastasis |
title_full | Nicaraven Attenuates Postoperative Systemic Inflammatory Responses-Induced Tumor Metastasis |
title_fullStr | Nicaraven Attenuates Postoperative Systemic Inflammatory Responses-Induced Tumor Metastasis |
title_full_unstemmed | Nicaraven Attenuates Postoperative Systemic Inflammatory Responses-Induced Tumor Metastasis |
title_short | Nicaraven Attenuates Postoperative Systemic Inflammatory Responses-Induced Tumor Metastasis |
title_sort | nicaraven attenuates postoperative systemic inflammatory responses-induced tumor metastasis |
topic | Translational Research and Biomarkers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7060163/ https://www.ncbi.nlm.nih.gov/pubmed/31873930 http://dx.doi.org/10.1245/s10434-019-08076-2 |
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