RSK3 switches cell fate: from stress-induced senescence to malignant progression.


Journal

Journal of experimental & clinical cancer research : CR
ISSN: 1756-9966
Titre abrégé: J Exp Clin Cancer Res
Pays: England
ID NLM: 8308647

Informations de publication

Date de publication:
27 Nov 2023
Historique:
received: 22 06 2023
accepted: 19 11 2023
medline: 28 11 2023
pubmed: 27 11 2023
entrez: 26 11 2023
Statut: epublish

Résumé

TGFβ induces several cell phenotypes including senescence, a stable cell cycle arrest accompanied by a secretory program, and epithelial-mesenchymal transition (EMT) in normal epithelial cells. During carcinogenesis cells lose the ability to undergo senescence in response to TGFβ but they maintain an EMT, which can contribute to tumor progression. Our aim was to identify mechanisms promoting TGFβ-induced senescence escape. In vitro experiments were performed with primary human mammary epithelial cells (HMEC) immortalized by hTert. For kinase library screen and modulation of gene expression retroviral transduction was used. To characterize gene expression, RNA microarray with GSEA analysis and RT-qPCR were used. For protein level and localization, Western blot and immunofluorescence were performed. For senescence characterization crystal violet assay, Senescence Associated-β-Galactosidase activity, EdU staining were conducted. To determine RSK3 partners FLAG-baited immunoprecipitation and mass spectrometry-based proteomic analyses were performed. Proteosome activity and proteasome enrichment assays were performed. To validate the role of RSK3 in human breast cancer, analysis of METABRIC database was performed. Murine intraductal xenografts using MCF10DCIS.com cells were carried out, with histological and immunofluorescence analysis of mouse tissue sections. A screen with active kinases in HMECs upon TGFβ treatment identified that the serine threonine kinase RSK3, or RPS6KA2, a kinase mainly known to regulate cancer cell death including in breast cancer, reverted TGFβ-induced senescence. Interestingly, RSK3 expression decreased in response to TGFβ in a SMAD3-dependent manner, and its constitutive expression rescued SMAD3-induced senescence, indicating that a decrease in RSK3 itself contributes to TGFβ-induced senescence. Using transcriptomic analyses and affinity purification coupled to mass spectrometry-based proteomics, we unveiled that RSK3 regulates senescence by inhibiting the NF-κΒ pathway through the decrease in proteasome-mediated IκBα degradation. Strikingly, senescent TGFβ-treated HMECs display features of epithelial to mesenchymal transition (EMT) and during RSK3-induced senescence escaped HMECs conserve EMT features. Importantly, RSK3 expression is correlated with EMT and invasion, and inversely correlated with senescence and NF-κΒ in human claudin-low breast tumors and its expression enhances the formation of breast invasive tumors in the mouse mammary gland. We conclude that RSK3 switches cell fate from senescence to malignancy in response to TGFβ signaling.

Sections du résumé

BACKGROUND BACKGROUND
TGFβ induces several cell phenotypes including senescence, a stable cell cycle arrest accompanied by a secretory program, and epithelial-mesenchymal transition (EMT) in normal epithelial cells. During carcinogenesis cells lose the ability to undergo senescence in response to TGFβ but they maintain an EMT, which can contribute to tumor progression. Our aim was to identify mechanisms promoting TGFβ-induced senescence escape.
METHODS METHODS
In vitro experiments were performed with primary human mammary epithelial cells (HMEC) immortalized by hTert. For kinase library screen and modulation of gene expression retroviral transduction was used. To characterize gene expression, RNA microarray with GSEA analysis and RT-qPCR were used. For protein level and localization, Western blot and immunofluorescence were performed. For senescence characterization crystal violet assay, Senescence Associated-β-Galactosidase activity, EdU staining were conducted. To determine RSK3 partners FLAG-baited immunoprecipitation and mass spectrometry-based proteomic analyses were performed. Proteosome activity and proteasome enrichment assays were performed. To validate the role of RSK3 in human breast cancer, analysis of METABRIC database was performed. Murine intraductal xenografts using MCF10DCIS.com cells were carried out, with histological and immunofluorescence analysis of mouse tissue sections.
RESULTS RESULTS
A screen with active kinases in HMECs upon TGFβ treatment identified that the serine threonine kinase RSK3, or RPS6KA2, a kinase mainly known to regulate cancer cell death including in breast cancer, reverted TGFβ-induced senescence. Interestingly, RSK3 expression decreased in response to TGFβ in a SMAD3-dependent manner, and its constitutive expression rescued SMAD3-induced senescence, indicating that a decrease in RSK3 itself contributes to TGFβ-induced senescence. Using transcriptomic analyses and affinity purification coupled to mass spectrometry-based proteomics, we unveiled that RSK3 regulates senescence by inhibiting the NF-κΒ pathway through the decrease in proteasome-mediated IκBα degradation. Strikingly, senescent TGFβ-treated HMECs display features of epithelial to mesenchymal transition (EMT) and during RSK3-induced senescence escaped HMECs conserve EMT features. Importantly, RSK3 expression is correlated with EMT and invasion, and inversely correlated with senescence and NF-κΒ in human claudin-low breast tumors and its expression enhances the formation of breast invasive tumors in the mouse mammary gland.
CONCLUSIONS CONCLUSIONS
We conclude that RSK3 switches cell fate from senescence to malignancy in response to TGFβ signaling.

Identifiants

pubmed: 38008756
doi: 10.1186/s13046-023-02909-5
pii: 10.1186/s13046-023-02909-5
pmc: PMC10680185
doi:

Substances chimiques

Proteasome Endopeptidase Complex EC 3.4.25.1
Transforming Growth Factor beta 0
ribosomal protein S6 kinase, 90kDa, polypeptide 3 EC 2.7.11.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

318

Subventions

Organisme : Institut National Du Cancer
ID : PLBio 18-144
Organisme : Institut National Du Cancer
ID : PLBio 15-013

Informations de copyright

© 2023. The Author(s).

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Auteurs

Anda Huna (A)

Cancer Research Center of Lyon, Inserm U1052, CNRS UMR 5286, Université de Lyon, Centre Léon Bérard, 69373, Lyon, France.
Equipe Labellisée La Ligue Contre Le Cancer, Lyon, France.

Jean-Michel Flaman (JM)

Cancer Research Center of Lyon, Inserm U1052, CNRS UMR 5286, Université de Lyon, Centre Léon Bérard, 69373, Lyon, France.
Equipe Labellisée La Ligue Contre Le Cancer, Lyon, France.

Catalina Lodillinsky (C)

INSERM UMR_S 938, Saint-Antoine Research Center, CRSA, University Sorbonne, Paris, France.
Research Area, Instituto de Oncología Ángel H. Roffo, Universidad de Buenos Aires, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentina.

Kexin Zhu (K)

Cancer Research Center of Lyon, Inserm U1052, CNRS UMR 5286, Université de Lyon, Centre Léon Bérard, 69373, Lyon, France.
Equipe Labellisée La Ligue Contre Le Cancer, Lyon, France.

Gabriela Makulyte (G)

Cancer Research Center of Lyon, Inserm U1052, CNRS UMR 5286, Université de Lyon, Centre Léon Bérard, 69373, Lyon, France.
Equipe Labellisée La Ligue Contre Le Cancer, Lyon, France.

Victoria Pakulska (V)

Université Grenoble Alpes, Inserm, UA13 BGE, CNRS, CEA, FR2048, 38000, Grenoble, France.

Yohann Coute (Y)

Université Grenoble Alpes, Inserm, UA13 BGE, CNRS, CEA, FR2048, 38000, Grenoble, France.

Clémence Ruisseaux (C)

Cancer Research Center of Lyon, Inserm U1052, CNRS UMR 5286, Université de Lyon, Centre Léon Bérard, 69373, Lyon, France.

Pierre Saintigny (P)

Cancer Research Center of Lyon, Inserm U1052, CNRS UMR 5286, Université de Lyon, Centre Léon Bérard, 69373, Lyon, France.

Hector Hernandez-Vargas (H)

Cancer Research Center of Lyon, Inserm U1052, CNRS UMR 5286, Université de Lyon, Centre Léon Bérard, 69373, Lyon, France.

Pierre-Antoine Defossez (PA)

Epigenetics and Cell Fate Centre, CNRS UMR 7216, Université Paris Diderot, Paris, France.

Mathieu Boissan (M)

INSERM UMR_S 938, Saint-Antoine Research Center, CRSA, University Sorbonne, Paris, France.

Nadine Martin (N)

Cancer Research Center of Lyon, Inserm U1052, CNRS UMR 5286, Université de Lyon, Centre Léon Bérard, 69373, Lyon, France.
Equipe Labellisée La Ligue Contre Le Cancer, Lyon, France.

David Bernard (D)

Cancer Research Center of Lyon, Inserm U1052, CNRS UMR 5286, Université de Lyon, Centre Léon Bérard, 69373, Lyon, France. david.bernard@lyon.unicancer.fr.
Equipe Labellisée La Ligue Contre Le Cancer, Lyon, France. david.bernard@lyon.unicancer.fr.

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