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Title:
Nuclear receptor NR4A1 promotes breast cancer invasion and metastasis by activating TGF-β signalling | Nature Communications
Description:
In advanced cancers, the TGF-β pathway acts as an oncogenic factor and is considered to be a therapeutic target. Here using a genome-wide cDNA screen, we identify nuclear receptor NR4A1 as a strong activator of TGF-β signalling. NR4A1 promotes TGF-β/SMAD signalling by facilitating AXIN2–RNF12/ARKADIA-induced SMAD7 degradation. NR4A1 interacts with SMAD7 and AXIN2, and potently and directly induces AXIN2 expression. Whereas loss of NR4A1 inhibits TGF-β-induced epithelial-to-mesenchymal transition and metastasis, slight NR4A1 ectopic expression stimulates metastasis in a TGF-β-dependent manner. Importantly, inflammatory cytokines potently induce NR4A1 expression, and potentiate TGF-β-mediated breast cancer cell migration, invasion and metastasis in vitro and in vivo. Notably, NR4A1 expression is elevated in breast cancer patients with high immune infiltration and its expression weakly correlates with phosphorylated SMAD2 levels, and is an indicator of poor prognosis. Our results uncover inflammation-induced NR4A1 as an important determinant for hyperactivation of pro-oncogenic TGF-β signalling in breast cancer. The TGF-β signalling pathway promotes cancer progression in late stage breast cancer, but how the pathway is activated is not always clear. In this study, Zhou et al.identify that the expression of nuclear receptor NR4A1 is induced by inflammation and is an activator of TGF-β-induced metastasis.
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nra, cells, smad, cancer, fig, expression, tgfβ, cell, article, axin, breast, google, scholar, signalling, cas, analysis, metastasis, supplementary, control, stably, nature, receptor, data, tgfβsmad, treated, immunoblot, mefs, expressing, degradation, tgfβinduced, tβri, mdamb, mouse, protein, activity, human, nuclear, invasion, mice, results, tumour, performed, found, ilβ, promotes, arkadia, transcriptional, depletion, shrna, time,
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nature portfolio scientific research permissions reprints special diet services privacy policy nr4a1-activated tgf-β/smad signalling regulating tgf-β/smad signalling tgf-β-induced epithelial-mesenchymal transition tgf-β-driven tumour progression36 facilitate tgf-β/smad signalling potentiating tgf-β/smad signalling author information authors nr4a1-depleted mda-mb-231/mcherry cells promote tgf-β-mediated emt smad3-smad4-driven transcriptional reporter smad7/arkadia/rnf12/axin2 complex endogenously nr4a1 potentiated tgf-β-induced open biosystems tgf-β-induced transcriptional response alexafluor593-labelled anti-rabbit antibody carboxy-terminal ligand-binding domain23 mcf10a-ras-transformed cell line advertising putative ngfi-b-response elements tgf-β/smad signal activation pro-oncogenic tgf-β signalling tgf-β-induced phospho-smad2 full access specific ngfi-b-response element tgf-β-induced epithelial tgf-β/smad signalling tgf-β-smad signalling social media activating tgf-β signalling axin2-induced smad3/smad4 response tgf-β-induced emt tgf-β receptor signalling fundamental research funds nr4a1-depleted mda-mb-231 cells tgf-β/smad activation tgf-β-induced effects tgf-β-induced expression tgf-β-dependent manner caga-luc transcriptional reporter tgf-β pathway acts activated tgf-β type smad7/pai-1/ctgf/cxcr4 expression jak1/stat1-mediated pathway aberrant force-induced osteoarthritis mitigating tgf-β signalling6
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description:In advanced cancers, the TGF-β pathway acts as an oncogenic factor and is considered to be a therapeutic target. Here using a genome-wide cDNA screen, we identify nuclear receptor NR4A1 as a strong activator of TGF-β signalling. NR4A1 promotes TGF-β/SMAD signalling by facilitating AXIN2âRNF12/ARKADIA-induced SMAD7 degradation. NR4A1 interacts with SMAD7 and AXIN2, and potently and directly induces AXIN2 expression. Whereas loss of NR4A1 inhibits TGF-β-induced epithelial-to-mesenchymal transition and metastasis, slight NR4A1 ectopic expression stimulates metastasis in a TGF-β-dependent manner. Importantly, inflammatory cytokines potently induce NR4A1 expression, and potentiate TGF-β-mediated breast cancer cell migration, invasion and metastasis in vitro and in vivo. Notably, NR4A1 expression is elevated in breast cancer patients with high immune infiltration and its expression weakly correlates with phosphorylated SMAD2 levels, and is an indicator of poor prognosis. Our results uncover inflammation-induced NR4A1 as an important determinant for hyperactivation of pro-oncogenic TGF-β signalling in breast cancer. The TGF-β signalling pathway promotes cancer progression in late stage breast cancer, but how the pathway is activated is not always clear. In this study, Zhou et al.identify that the expression of nuclear receptor NR4A1 is induced by inflammation and is an activator of TGF-β-induced metastasis.
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headline:Nuclear receptor NR4A1 promotes breast cancer invasion and metastasis by activating TGF-β signalling
description:In advanced cancers, the TGF-β pathway acts as an oncogenic factor and is considered to be a therapeutic target. Here using a genome-wide cDNA screen, we identify nuclear receptor NR4A1 as a strong activator of TGF-β signalling. NR4A1 promotes TGF-β/SMAD signalling by facilitating AXIN2âRNF12/ARKADIA-induced SMAD7 degradation. NR4A1 interacts with SMAD7 and AXIN2, and potently and directly induces AXIN2 expression. Whereas loss of NR4A1 inhibits TGF-β-induced epithelial-to-mesenchymal transition and metastasis, slight NR4A1 ectopic expression stimulates metastasis in a TGF-β-dependent manner. Importantly, inflammatory cytokines potently induce NR4A1 expression, and potentiate TGF-β-mediated breast cancer cell migration, invasion and metastasis in vitro and in vivo. Notably, NR4A1 expression is elevated in breast cancer patients with high immune infiltration and its expression weakly correlates with phosphorylated SMAD2 levels, and is an indicator of poor prognosis. Our results uncover inflammation-induced NR4A1 as an important determinant for hyperactivation of pro-oncogenic TGF-β signalling in breast cancer. The TGF-β signalling pathway promotes cancer progression in late stage breast cancer, but how the pathway is activated is not always clear. In this study, Zhou et al.identify that the expression of nuclear receptor NR4A1 is induced by inflammation and is an activator of TGF-β-induced metastasis.
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name:Department of Molecular Cell Biology, Cancer Genomics Centre Netherlands and Centre for Biomedical Genetics, Leiden University Medical Center, The Netherlands
type:PostalAddress
type:Organization
name:Yihao Li
affiliation:
name:Cancer Genomics Centre Netherlands and Centre for Biomedical Genetics, Leiden University Medical Center
address:
name:Department of Molecular Cell Biology, Cancer Genomics Centre Netherlands and Centre for Biomedical Genetics, Leiden University Medical Center, The Netherlands
type:PostalAddress
type:Organization
name:Lukas J. A. C. Hawinkels
affiliation:
name:Cancer Genomics Centre Netherlands and Centre for Biomedical Genetics, Leiden University Medical Center
address:
name:Department of Molecular Cell Biology, Cancer Genomics Centre Netherlands and Centre for Biomedical Genetics, Leiden University Medical Center, The Netherlands
type:PostalAddress
type:Organization
name:Kelly-Ann Sheppard
affiliation:
name:Novartis Institutes for Biomedical Research
address:
name:Novartis Institutes for Biomedical Research, Cambridge, USA
type:PostalAddress
type:Organization
name:Marie-José Goumans
affiliation:
name:Cancer Genomics Centre Netherlands and Centre for Biomedical Genetics, Leiden University Medical Center
address:
name:Department of Molecular Cell Biology, Cancer Genomics Centre Netherlands and Centre for Biomedical Genetics, Leiden University Medical Center, The Netherlands
type:PostalAddress
type:Organization
name:Rodney B. Luwor
affiliation:
name:The University of Melbourne, The Royal Melbourne Hospital 5th Floor Clinical Science Building
address:
name:Department of Surgery, The University of Melbourne, The Royal Melbourne Hospital 5th Floor Clinical Science Building, Parkville, Victoria, Australia
type:PostalAddress
type:Organization
name:Carlie J. de Vries
affiliation:
name:Academic Medical Center, K1-113, University of Amsterdam
address:
name:Academic Medical Center, K1-113, University of Amsterdam, Amsterdam, The Netherlands
type:PostalAddress
type:Organization
name:Wilma E. Mesker
affiliation:
name:Leiden University Medical Center
address:
name:Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands
type:PostalAddress
type:Organization
name:Rob A. E. M. Tollenaar
affiliation:
name:Leiden University Medical Center
address:
name:Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands
type:PostalAddress
type:Organization
name:Peter Devilee
affiliation:
name:Leiden University Medical Center
address:
name:Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands
type:PostalAddress
type:Organization
name:Chris X. Lu
affiliation:
name:Novartis Institutes for Biomedical Research
address:
name:Novartis Institutes for Biomedical Research, Cambridge, USA
type:PostalAddress
type:Organization
name:Hongjian Zhu
affiliation:
name:The University of Melbourne, The Royal Melbourne Hospital 5th Floor Clinical Science Building
address:
name:Department of Surgery, The University of Melbourne, The Royal Melbourne Hospital 5th Floor Clinical Science Building, Parkville, Victoria, Australia
type:PostalAddress
type:Organization
name:Long Zhang
affiliation:
name:Life Sciences Institute, Zhejiang University
address:
name:Life Sciences Institute, Zhejiang University, Hangzhou, China
type:PostalAddress
type:Organization
email:[email protected]
name:Peter ten Dijke
affiliation:
name:Life Sciences Institute, Zhejiang University
address:
name:Life Sciences Institute, Zhejiang University, Hangzhou, China
type:PostalAddress
type:Organization
name:Cancer Genomics Centre Netherlands and Centre for Biomedical Genetics, Leiden University Medical Center
address:
name:Department of Molecular Cell Biology, Cancer Genomics Centre Netherlands and Centre for Biomedical Genetics, Leiden University Medical Center, The Netherlands
type:PostalAddress
type:Organization
email:[email protected]
PostalAddress:
name:Life Sciences Institute, Zhejiang University, Hangzhou, China
name:Department of Molecular Cell Biology, Cancer Genomics Centre Netherlands and Centre for Biomedical Genetics, Leiden University Medical Center, The Netherlands
name:Department of Molecular Cell Biology, Cancer Genomics Centre Netherlands and Centre for Biomedical Genetics, Leiden University Medical Center, The Netherlands
name:Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands
name:Department of Molecular Cell Biology, Cancer Genomics Centre Netherlands and Centre for Biomedical Genetics, Leiden University Medical Center, The Netherlands
name:Department of Molecular Cell Biology, Cancer Genomics Centre Netherlands and Centre for Biomedical Genetics, Leiden University Medical Center, The Netherlands
name:Department of Molecular Cell Biology, Cancer Genomics Centre Netherlands and Centre for Biomedical Genetics, Leiden University Medical Center, The Netherlands
name:Novartis Institutes for Biomedical Research, Cambridge, USA
name:Department of Molecular Cell Biology, Cancer Genomics Centre Netherlands and Centre for Biomedical Genetics, Leiden University Medical Center, The Netherlands
name:Department of Surgery, The University of Melbourne, The Royal Melbourne Hospital 5th Floor Clinical Science Building, Parkville, Victoria, Australia
name:Academic Medical Center, K1-113, University of Amsterdam, Amsterdam, The Netherlands
name:Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands
name:Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands
name:Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands
name:Novartis Institutes for Biomedical Research, Cambridge, USA
name:Department of Surgery, The University of Melbourne, The Royal Melbourne Hospital 5th Floor Clinical Science Building, Parkville, Victoria, Australia
name:Life Sciences Institute, Zhejiang University, Hangzhou, China
name:Life Sciences Institute, Zhejiang University, Hangzhou, China
name:Department of Molecular Cell Biology, Cancer Genomics Centre Netherlands and Centre for Biomedical Genetics, Leiden University Medical Center, The Netherlands
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