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MAPK4 silencing in gastric cancer drives liver metastasis by positive feedback between cancer cells and macrophages

Liver metastasis is a major cause of death in gastric cancer patients, but the underlying mechanisms are poorly understood. Through a combination of in vivo screening and transcriptome profiling followed by quantitative RT-PCR and tissue array analyses, we found that mitogen-activated protein kinase...

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Autores principales: Li, Shuang, Guo, Dongyang, Sun, Qiang, Zhang, Lu, Cui, Yun, Liu, Min, Ma, Xixi, Liu, Yiman, Cui, Wenyu, Sun, Leimin, Teng, Lisong, Wang, Liangjing, Lin, Aifu, Liu, Wei, Zhuo, Wei, Zhou, Tianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981715/
https://www.ncbi.nlm.nih.gov/pubmed/36797541
http://dx.doi.org/10.1038/s12276-023-00946-w
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author Li, Shuang
Guo, Dongyang
Sun, Qiang
Zhang, Lu
Cui, Yun
Liu, Min
Ma, Xixi
Liu, Yiman
Cui, Wenyu
Sun, Leimin
Teng, Lisong
Wang, Liangjing
Lin, Aifu
Liu, Wei
Zhuo, Wei
Zhou, Tianhua
author_facet Li, Shuang
Guo, Dongyang
Sun, Qiang
Zhang, Lu
Cui, Yun
Liu, Min
Ma, Xixi
Liu, Yiman
Cui, Wenyu
Sun, Leimin
Teng, Lisong
Wang, Liangjing
Lin, Aifu
Liu, Wei
Zhuo, Wei
Zhou, Tianhua
author_sort Li, Shuang
collection PubMed
description Liver metastasis is a major cause of death in gastric cancer patients, but the underlying mechanisms are poorly understood. Through a combination of in vivo screening and transcriptome profiling followed by quantitative RT-PCR and tissue array analyses, we found that mitogen-activated protein kinase 4 (MAPK4) downregulation in gastric cancer tissues from patients is significantly associated with liver metastasis and poor prognosis. The knockdown of MAPK4 in gastric cancer cells promotes liver metastasis in orthotopic mouse models. MAPK4 depletion in gastric cancer cells induces the secretion of macrophage migration inhibitory factor (MIF) to polarize tumor-associated macrophages (TAMs) in orthotopic xenograft tumors. Moreover, TAMs activate epithelial–mesenchymal transition of gastric cancer cells to suppress MAPK4 expression, which further increases MIF secretion to polarize TAMs. Taken together, our results suggest a previously undescribed positive feedback loop between cancer cells and macrophages mediated by MAPK4 silencing that facilitates gastric cancer liver metastasis.
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spelling pubmed-99817152023-03-04 MAPK4 silencing in gastric cancer drives liver metastasis by positive feedback between cancer cells and macrophages Li, Shuang Guo, Dongyang Sun, Qiang Zhang, Lu Cui, Yun Liu, Min Ma, Xixi Liu, Yiman Cui, Wenyu Sun, Leimin Teng, Lisong Wang, Liangjing Lin, Aifu Liu, Wei Zhuo, Wei Zhou, Tianhua Exp Mol Med Article Liver metastasis is a major cause of death in gastric cancer patients, but the underlying mechanisms are poorly understood. Through a combination of in vivo screening and transcriptome profiling followed by quantitative RT-PCR and tissue array analyses, we found that mitogen-activated protein kinase 4 (MAPK4) downregulation in gastric cancer tissues from patients is significantly associated with liver metastasis and poor prognosis. The knockdown of MAPK4 in gastric cancer cells promotes liver metastasis in orthotopic mouse models. MAPK4 depletion in gastric cancer cells induces the secretion of macrophage migration inhibitory factor (MIF) to polarize tumor-associated macrophages (TAMs) in orthotopic xenograft tumors. Moreover, TAMs activate epithelial–mesenchymal transition of gastric cancer cells to suppress MAPK4 expression, which further increases MIF secretion to polarize TAMs. Taken together, our results suggest a previously undescribed positive feedback loop between cancer cells and macrophages mediated by MAPK4 silencing that facilitates gastric cancer liver metastasis. Nature Publishing Group UK 2023-02-17 /pmc/articles/PMC9981715/ /pubmed/36797541 http://dx.doi.org/10.1038/s12276-023-00946-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Li, Shuang
Guo, Dongyang
Sun, Qiang
Zhang, Lu
Cui, Yun
Liu, Min
Ma, Xixi
Liu, Yiman
Cui, Wenyu
Sun, Leimin
Teng, Lisong
Wang, Liangjing
Lin, Aifu
Liu, Wei
Zhuo, Wei
Zhou, Tianhua
MAPK4 silencing in gastric cancer drives liver metastasis by positive feedback between cancer cells and macrophages
title MAPK4 silencing in gastric cancer drives liver metastasis by positive feedback between cancer cells and macrophages
title_full MAPK4 silencing in gastric cancer drives liver metastasis by positive feedback between cancer cells and macrophages
title_fullStr MAPK4 silencing in gastric cancer drives liver metastasis by positive feedback between cancer cells and macrophages
title_full_unstemmed MAPK4 silencing in gastric cancer drives liver metastasis by positive feedback between cancer cells and macrophages
title_short MAPK4 silencing in gastric cancer drives liver metastasis by positive feedback between cancer cells and macrophages
title_sort mapk4 silencing in gastric cancer drives liver metastasis by positive feedback between cancer cells and macrophages
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981715/
https://www.ncbi.nlm.nih.gov/pubmed/36797541
http://dx.doi.org/10.1038/s12276-023-00946-w
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