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SMYD2 targets RIPK1 and restricts TNF-induced apoptosis and necroptosis to support colon tumor growth

SMYD2 is a histone methyltransferase, which methylates both histone H3K4 as well as a number of non-histone proteins. Dysregulation of SMYD2 has been associated with several diseases including cancer. In the present study, we investigated whether and how SMYD2 might contribute to colorectal cancer....

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Autores principales: Yu, Yu-qiang, Thonn, Veronika, Patankar, Jay V., Thoma, Oana-Maria, Waldner, Maximilian, Zielinska, Marta, Bao, Li-li, Gonzalez-Acera, Miguel, Wallmüller, Stefan, Engel, Felix B., Stürzl, Michael, Neurath, Markus F., Liebing, Eva, Becker, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755774/
https://www.ncbi.nlm.nih.gov/pubmed/35022391
http://dx.doi.org/10.1038/s41419-021-04483-0
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author Yu, Yu-qiang
Thonn, Veronika
Patankar, Jay V.
Thoma, Oana-Maria
Waldner, Maximilian
Zielinska, Marta
Bao, Li-li
Gonzalez-Acera, Miguel
Wallmüller, Stefan
Engel, Felix B.
Stürzl, Michael
Neurath, Markus F.
Liebing, Eva
Becker, Christoph
author_facet Yu, Yu-qiang
Thonn, Veronika
Patankar, Jay V.
Thoma, Oana-Maria
Waldner, Maximilian
Zielinska, Marta
Bao, Li-li
Gonzalez-Acera, Miguel
Wallmüller, Stefan
Engel, Felix B.
Stürzl, Michael
Neurath, Markus F.
Liebing, Eva
Becker, Christoph
author_sort Yu, Yu-qiang
collection PubMed
description SMYD2 is a histone methyltransferase, which methylates both histone H3K4 as well as a number of non-histone proteins. Dysregulation of SMYD2 has been associated with several diseases including cancer. In the present study, we investigated whether and how SMYD2 might contribute to colorectal cancer. Increased expression levels of SMYD2 were detected in human and murine colon tumor tissues compared to tumor-free tissues. SMYD2 deficiency in colonic tumor cells strongly decreased tumor growth in two independent experimental cancer models. On a molecular level, SMYD2 deficiency sensitized colonic tumor cells to TNF-induced apoptosis and necroptosis without affecting cell proliferation. Moreover, we found that SMYD2 targeted RIPK1 and inhibited the phosphorylation of RIPK1. Finally, in a translational approach, pharmacological inhibition of SMYD2 attenuated colonic tumor growth. Collectively, our data show that SMYD2 is crucial for colon tumor growth and inhibits TNF-induced apoptosis and necroptosis.
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spelling pubmed-87557742022-01-20 SMYD2 targets RIPK1 and restricts TNF-induced apoptosis and necroptosis to support colon tumor growth Yu, Yu-qiang Thonn, Veronika Patankar, Jay V. Thoma, Oana-Maria Waldner, Maximilian Zielinska, Marta Bao, Li-li Gonzalez-Acera, Miguel Wallmüller, Stefan Engel, Felix B. Stürzl, Michael Neurath, Markus F. Liebing, Eva Becker, Christoph Cell Death Dis Article SMYD2 is a histone methyltransferase, which methylates both histone H3K4 as well as a number of non-histone proteins. Dysregulation of SMYD2 has been associated with several diseases including cancer. In the present study, we investigated whether and how SMYD2 might contribute to colorectal cancer. Increased expression levels of SMYD2 were detected in human and murine colon tumor tissues compared to tumor-free tissues. SMYD2 deficiency in colonic tumor cells strongly decreased tumor growth in two independent experimental cancer models. On a molecular level, SMYD2 deficiency sensitized colonic tumor cells to TNF-induced apoptosis and necroptosis without affecting cell proliferation. Moreover, we found that SMYD2 targeted RIPK1 and inhibited the phosphorylation of RIPK1. Finally, in a translational approach, pharmacological inhibition of SMYD2 attenuated colonic tumor growth. Collectively, our data show that SMYD2 is crucial for colon tumor growth and inhibits TNF-induced apoptosis and necroptosis. Nature Publishing Group UK 2022-01-12 /pmc/articles/PMC8755774/ /pubmed/35022391 http://dx.doi.org/10.1038/s41419-021-04483-0 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
Yu, Yu-qiang
Thonn, Veronika
Patankar, Jay V.
Thoma, Oana-Maria
Waldner, Maximilian
Zielinska, Marta
Bao, Li-li
Gonzalez-Acera, Miguel
Wallmüller, Stefan
Engel, Felix B.
Stürzl, Michael
Neurath, Markus F.
Liebing, Eva
Becker, Christoph
SMYD2 targets RIPK1 and restricts TNF-induced apoptosis and necroptosis to support colon tumor growth
title SMYD2 targets RIPK1 and restricts TNF-induced apoptosis and necroptosis to support colon tumor growth
title_full SMYD2 targets RIPK1 and restricts TNF-induced apoptosis and necroptosis to support colon tumor growth
title_fullStr SMYD2 targets RIPK1 and restricts TNF-induced apoptosis and necroptosis to support colon tumor growth
title_full_unstemmed SMYD2 targets RIPK1 and restricts TNF-induced apoptosis and necroptosis to support colon tumor growth
title_short SMYD2 targets RIPK1 and restricts TNF-induced apoptosis and necroptosis to support colon tumor growth
title_sort smyd2 targets ripk1 and restricts tnf-induced apoptosis and necroptosis to support colon tumor growth
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755774/
https://www.ncbi.nlm.nih.gov/pubmed/35022391
http://dx.doi.org/10.1038/s41419-021-04483-0
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