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Hepatocyte growth factor derived from senescent cells attenuates cell competition-induced apical elimination of oncogenic cells

Cellular senescence and cell competition are important tumor suppression mechanisms that restrain cells with oncogenic mutations at the initial stage of cancer development. However, the link between cellular senescence and cell competition remains unclear. Senescent cells accumulated during the in v...

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Autores principales: Igarashi, Nanase, Miyata, Kenichi, Loo, Tze Mun, Chiba, Masatomo, Hanyu, Aki, Nishio, Mika, Kawasaki, Hiroko, Zheng, Hao, Toyokuni, Shinya, Kon, Shunsuke, Moriyama, Keiji, Fujita, Yasuyuki, Takahashi, Akiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9293948/
https://www.ncbi.nlm.nih.gov/pubmed/35851277
http://dx.doi.org/10.1038/s41467-022-31642-4
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author Igarashi, Nanase
Miyata, Kenichi
Loo, Tze Mun
Chiba, Masatomo
Hanyu, Aki
Nishio, Mika
Kawasaki, Hiroko
Zheng, Hao
Toyokuni, Shinya
Kon, Shunsuke
Moriyama, Keiji
Fujita, Yasuyuki
Takahashi, Akiko
author_facet Igarashi, Nanase
Miyata, Kenichi
Loo, Tze Mun
Chiba, Masatomo
Hanyu, Aki
Nishio, Mika
Kawasaki, Hiroko
Zheng, Hao
Toyokuni, Shinya
Kon, Shunsuke
Moriyama, Keiji
Fujita, Yasuyuki
Takahashi, Akiko
author_sort Igarashi, Nanase
collection PubMed
description Cellular senescence and cell competition are important tumor suppression mechanisms that restrain cells with oncogenic mutations at the initial stage of cancer development. However, the link between cellular senescence and cell competition remains unclear. Senescent cells accumulated during the in vivo aging process contribute toward age-related cancers via the development of senescence-associated secretory phenotype (SASP). Here, we report that hepatocyte growth factor (HGF), a SASP factor, inhibits apical extrusion and promotes basal protrusion of Ras-mutated cells in the cell competition assay. Additionally, cellular senescence induced by a high-fat diet promotes the survival of cells with oncogenic mutations, whereas crizotinib, an inhibitor of HGF signaling, provokes the removal of mutated cells from mouse livers and intestines. Our study provides evidence that cellular senescence inhibits cell competition-mediated elimination of oncogenic cells through HGF signaling, suggesting that it may lead to cancer incidence during aging.
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spelling pubmed-92939482022-07-20 Hepatocyte growth factor derived from senescent cells attenuates cell competition-induced apical elimination of oncogenic cells Igarashi, Nanase Miyata, Kenichi Loo, Tze Mun Chiba, Masatomo Hanyu, Aki Nishio, Mika Kawasaki, Hiroko Zheng, Hao Toyokuni, Shinya Kon, Shunsuke Moriyama, Keiji Fujita, Yasuyuki Takahashi, Akiko Nat Commun Article Cellular senescence and cell competition are important tumor suppression mechanisms that restrain cells with oncogenic mutations at the initial stage of cancer development. However, the link between cellular senescence and cell competition remains unclear. Senescent cells accumulated during the in vivo aging process contribute toward age-related cancers via the development of senescence-associated secretory phenotype (SASP). Here, we report that hepatocyte growth factor (HGF), a SASP factor, inhibits apical extrusion and promotes basal protrusion of Ras-mutated cells in the cell competition assay. Additionally, cellular senescence induced by a high-fat diet promotes the survival of cells with oncogenic mutations, whereas crizotinib, an inhibitor of HGF signaling, provokes the removal of mutated cells from mouse livers and intestines. Our study provides evidence that cellular senescence inhibits cell competition-mediated elimination of oncogenic cells through HGF signaling, suggesting that it may lead to cancer incidence during aging. Nature Publishing Group UK 2022-07-18 /pmc/articles/PMC9293948/ /pubmed/35851277 http://dx.doi.org/10.1038/s41467-022-31642-4 Text en © The Author(s) 2022 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
Igarashi, Nanase
Miyata, Kenichi
Loo, Tze Mun
Chiba, Masatomo
Hanyu, Aki
Nishio, Mika
Kawasaki, Hiroko
Zheng, Hao
Toyokuni, Shinya
Kon, Shunsuke
Moriyama, Keiji
Fujita, Yasuyuki
Takahashi, Akiko
Hepatocyte growth factor derived from senescent cells attenuates cell competition-induced apical elimination of oncogenic cells
title Hepatocyte growth factor derived from senescent cells attenuates cell competition-induced apical elimination of oncogenic cells
title_full Hepatocyte growth factor derived from senescent cells attenuates cell competition-induced apical elimination of oncogenic cells
title_fullStr Hepatocyte growth factor derived from senescent cells attenuates cell competition-induced apical elimination of oncogenic cells
title_full_unstemmed Hepatocyte growth factor derived from senescent cells attenuates cell competition-induced apical elimination of oncogenic cells
title_short Hepatocyte growth factor derived from senescent cells attenuates cell competition-induced apical elimination of oncogenic cells
title_sort hepatocyte growth factor derived from senescent cells attenuates cell competition-induced apical elimination of oncogenic cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9293948/
https://www.ncbi.nlm.nih.gov/pubmed/35851277
http://dx.doi.org/10.1038/s41467-022-31642-4
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