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  1. Book ; Online: Regulation of Tissue Responses: The TWEAK/Fn14 Pathway and other TNF/ TNFR Superfamily Members that Activate Noncanonical NFkB Signaling

    Zheng, Timothy S. / Burkly, Linda C. / Silke, John

    2016  

    Abstract: The immune system mediates tissue responses under both physiological and pathological conditions, impacting the inflammatory, fibrogenic and regenerative components. In addition to various leukocyte subsets, it is now recognized that epithelial, ... ...

    Abstract The immune system mediates tissue responses under both physiological and pathological conditions, impacting the inflammatory, fibrogenic and regenerative components. In addition to various leukocyte subsets, it is now recognized that epithelial, endothelial and other non-hematopoietic tissue cell types actively contribute to the interplay shaping tissue responses. Further understanding the molecular pathways and mechanisms mediating these tissue responses is of great interest. In the past decade, TNF-like weak inducer of apoptosis (TWEAK) and its receptor, FGF-inducible molecule-14 (Fn14), members of the TNF/TNFR superfamily, have emerged as a prominent molecular axis regulating tissue responses.-

    Generally leukocyte-derived, TWEAK signals through Fn14 which is highly induced in injured and diseased tissues on the surface of parenchymal, stromal and progenitor cells, thereby orchestrating a host of tissue-shaping responses, including inflammation, angiogenesis, cell proliferation or death, and the regulation of progenitor cells. Compelling preclinical results indicate that whereas transient TWEAK/Fn14 activation promotes productive tissue responses after acute injury, excessive or persistent TWEAK/Fn14 activation drives pathological tissue responses, leading to progressive damage and degeneration in target organs of injury, autoimmune and inflammatory diseases and cancer. Given that the highly inducible pattern of Fn14 expression is well conserved between mouse and man, the role of TWEAK/Fn14 in human disease is an area of intense investigation.-

    Recent findings have also begun to shed light on how the TWEAK/Fn14 pathway fits into the immune network, interplaying with other well-established pathways, including TNFa, IL-17, IL-13 and TGFb, in regulating tissue responses. The noncanonical nuclear factor kB (NF?B) pathway plays a role in immunity and disease pathologies and appears to be activated by only a subset of TNF/ TNFR superfamily members. Of the various signaling pathways downstream of TWEAK/Fn14, particular attention has been placed on the noncanonical NF?B pathway given that given that TWEAK induces acute activation of canonical NF?B but prolonged activation of noncanonical pathway. Thus dovetailing of the TWEAK/Fn14 axis with noncanonical NF?B pathway activation may be a key mechanism underlying tissue responses. Also of great interest is a deeper understanding of where, when and how tissue responses are regulated by other TNF/ TNFR superfamily members that can signal through noncanonical NF?B.-
    Keywords Immunologic diseases. Allergy ; Medicine (General)
    Size 1 electronic resource (201 p.)
    Publisher Frontiers Media SA
    Document type Book ; Online
    Note English ; Open Access
    HBZ-ID HT020091132
    ISBN 9782889197002 ; 288919700X
    Database ZB MED Catalogue: Medicine, Health, Nutrition, Environment, Agriculture

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  2. Article ; Online: RIPK1 and necroptosis role in premature ageing.

    Wang, Panxue / Silke, John

    Nature cell biology

    2024  Volume 26, Issue 4, Page(s) 508–509

    MeSH term(s) Humans ; Necroptosis ; Necrosis ; Apoptosis ; Aging/genetics ; Receptor-Interacting Protein Serine-Threonine Kinases/genetics ; Receptor-Interacting Protein Serine-Threonine Kinases/metabolism
    Chemical Substances Receptor-Interacting Protein Serine-Threonine Kinases (EC 2.7.11.1) ; RIPK1 protein, human (EC 2.7.11.1)
    Language English
    Publishing date 2024-03-27
    Publishing country England
    Document type Journal Article
    ZDB-ID 1474722-4
    ISSN 1476-4679 ; 1465-7392
    ISSN (online) 1476-4679
    ISSN 1465-7392
    DOI 10.1038/s41556-024-01390-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Blocking cell death limits lung damage and inflammation from influenza.

    Gupta, Nishma / Silke, John

    Nature

    2024  Volume 628, Issue 8009, Page(s) 726–727

    MeSH term(s) Animals ; Humans ; Influenza, Human/virology ; Influenza, Human/immunology ; Mice ; Lung/pathology ; Lung/immunology ; Lung/virology ; Inflammation/pathology ; Inflammation/immunology ; Cell Death ; Orthomyxoviridae Infections/virology ; Orthomyxoviridae Infections/immunology ; Orthomyxoviridae Infections/pathology
    Language English
    Publishing date 2024-04-10
    Publishing country England
    Document type News
    ZDB-ID 120714-3
    ISSN 1476-4687 ; 0028-0836
    ISSN (online) 1476-4687
    ISSN 0028-0836
    DOI 10.1038/d41586-024-00910-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Necroptosis in chronic obstructive pulmonary disease, a smoking gun?

    Pierotti, Catia L / Silke, John

    Immunology and cell biology

    2022  Volume 100, Issue 2, Page(s) 79–82

    Abstract: Recent studies, reviewed here, using a cigarette smoke exposure model for chronic obstructive pulmonary disease (COPD) in Ripk3 and Mlkl knock-out mice, and correlation with patient samples, suggest necroptosis plays a pathophysiological role in COPD by ... ...

    Abstract Recent studies, reviewed here, using a cigarette smoke exposure model for chronic obstructive pulmonary disease (COPD) in Ripk3 and Mlkl knock-out mice, and correlation with patient samples, suggest necroptosis plays a pathophysiological role in COPD by promoting inflammation, airway remodeling and emphysema.
    MeSH term(s) Airway Remodeling ; Animals ; Disease Models, Animal ; Humans ; Inflammation ; Lung ; Mice ; Necroptosis ; Pulmonary Disease, Chronic Obstructive ; Pulmonary Emphysema
    Language English
    Publishing date 2022-01-12
    Publishing country United States
    Document type Journal Article
    ZDB-ID 284057-1
    ISSN 1440-1711 ; 0818-9641
    ISSN (online) 1440-1711
    ISSN 0818-9641
    DOI 10.1111/imcb.12515
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Immunogenic cell death in cancer: targeting necroptosis to induce antitumour immunity.

    Meier, Pascal / Legrand, Arnaud J / Adam, Dieter / Silke, John

    Nature reviews. Cancer

    2024  Volume 24, Issue 5, Page(s) 299–315

    Abstract: Most metastatic cancers remain incurable due to the emergence of apoptosis-resistant clones, fuelled by intratumour heterogeneity and tumour evolution. To improve treatment, therapies should not only kill cancer cells but also activate the immune system ... ...

    Abstract Most metastatic cancers remain incurable due to the emergence of apoptosis-resistant clones, fuelled by intratumour heterogeneity and tumour evolution. To improve treatment, therapies should not only kill cancer cells but also activate the immune system against the tumour to eliminate any residual cancer cells that survive treatment. While current cancer therapies rely heavily on apoptosis - a largely immunologically silent form of cell death - there is growing interest in harnessing immunogenic forms of cell death such as necroptosis. Unlike apoptosis, necroptosis generates second messengers that act on immune cells in the tumour microenvironment, alerting them of danger. This lytic form of cell death optimizes the provision of antigens and adjuvanticity for immune cells, potentially boosting anticancer treatment approaches by combining cellular suicide and immune response approaches. In this Review, we discuss the mechanisms of necroptosis and how it activates antigen-presenting cells, drives cross-priming of CD8
    MeSH term(s) Humans ; Necroptosis/immunology ; Neoplasms/immunology ; Neoplasms/pathology ; Immunogenic Cell Death ; Tumor Microenvironment/immunology ; Animals ; CD8-Positive T-Lymphocytes/immunology ; Immunotherapy/methods
    Language English
    Publishing date 2024-03-07
    Publishing country England
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 2062767-1
    ISSN 1474-1768 ; 1474-175X
    ISSN (online) 1474-1768
    ISSN 1474-175X
    DOI 10.1038/s41568-024-00674-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: RIPK3 cleavage is dispensable for necroptosis inhibition but restricts NLRP3 inflammasome activation.

    Tran, Hong Tri / Kratina, Tobias / Coutansais, Auriane / Michalek, Dominika / Hogan, Benjamin M / Lawlor, Kate E / Vince, James E / Silke, John / Lalaoui, Najoua

    Cell death and differentiation

    2024  Volume 31, Issue 5, Page(s) 662–671

    Abstract: Caspase-8 activity is required to inhibit necroptosis during embryogenesis in mice. In vitro studies have suggested that caspase-8 directly cleaves RIPK1, CYLD and the key necroptotic effector kinase RIPK3 to repress necroptosis. However, recent studies ... ...

    Abstract Caspase-8 activity is required to inhibit necroptosis during embryogenesis in mice. In vitro studies have suggested that caspase-8 directly cleaves RIPK1, CYLD and the key necroptotic effector kinase RIPK3 to repress necroptosis. However, recent studies have shown that mice expressing uncleavable RIPK1 die during embryogenesis due to excessive apoptosis, while uncleavable CYLD mice are viable. Therefore, these results raise important questions about the role of RIPK3 cleavage. To evaluate the physiological significance of RIPK3 cleavage, we generated Ripk3
    MeSH term(s) Animals ; Receptor-Interacting Protein Serine-Threonine Kinases/metabolism ; Necroptosis ; Inflammasomes/metabolism ; NLR Family, Pyrin Domain-Containing 3 Protein/metabolism ; Caspase 8/metabolism ; Mice ; Mice, Inbred C57BL ; Interleukin-1beta/metabolism ; Pyroptosis
    Language English
    Publishing date 2024-03-21
    Publishing country England
    Document type Journal Article
    ZDB-ID 1225672-9
    ISSN 1476-5403 ; 1350-9047
    ISSN (online) 1476-5403
    ISSN 1350-9047
    DOI 10.1038/s41418-024-01281-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Digesting the Role of JAK-STAT and Cytokine Signaling in Oral and Gastric Cancers.

    Ni, Yanhong / Low, Jun T / Silke, John / O'Reilly, Lorraine A

    Frontiers in immunology

    2022  Volume 13, Page(s) 835997

    Abstract: When small proteins such as cytokines bind to their associated receptors on the plasma membrane, they can activate multiple internal signaling cascades allowing information from one cell to affect another. Frequently the signaling cascade leads to a ... ...

    Abstract When small proteins such as cytokines bind to their associated receptors on the plasma membrane, they can activate multiple internal signaling cascades allowing information from one cell to affect another. Frequently the signaling cascade leads to a change in gene expression that can affect cell functions such as proliferation, differentiation and homeostasis. The Janus kinase-signal transducer and activator of transcription (JAK-STAT) and the tumor necrosis factor receptor (TNFR) are the pivotal mechanisms employed for such communication. When deregulated, the JAK-STAT and the TNF receptor signaling pathways can induce chronic inflammatory phenotypes by promoting more cytokine production. Furthermore, these signaling pathways can promote replication, survival and metastasis of cancer cells. This review will summarize the essentials of the JAK/STAT and TNF signaling pathways and their regulation and the molecular mechanisms that lead to the dysregulation of the JAK-STAT pathway. The consequences of dysregulation, as ascertained from founding work in haematopoietic malignancies to more recent research in solid oral-gastrointestinal cancers, will also be discussed. Finally, this review will highlight the development and future of therapeutic applications which modulate the JAK-STAT or the TNF signaling pathways in cancers.
    MeSH term(s) Cytokines/metabolism ; Humans ; Janus Kinases/metabolism ; STAT Transcription Factors/metabolism ; Signal Transduction ; Stomach Neoplasms
    Chemical Substances Cytokines ; STAT Transcription Factors ; Janus Kinases (EC 2.7.10.2)
    Language English
    Publishing date 2022-06-29
    Publishing country Switzerland
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2022.835997
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: NF-κB and Pancreatic Cancer; Chapter and Verse.

    Silke, John / O'Reilly, Lorraine Ann

    Cancers

    2021  Volume 13, Issue 18

    Abstract: Pancreatic Ductal Adenocarcinoma (PDAC) is one of the world's most lethal cancers. An increase in occurrence, coupled with, presently limited treatment options, necessitates the pursuit of new therapeutic approaches. Many human cancers, including PDAC ... ...

    Abstract Pancreatic Ductal Adenocarcinoma (PDAC) is one of the world's most lethal cancers. An increase in occurrence, coupled with, presently limited treatment options, necessitates the pursuit of new therapeutic approaches. Many human cancers, including PDAC are initiated by unresolved inflammation. The transcription factor NF-κB coordinates many signals that drive cellular activation and proliferation during immunity but also those involved in inflammation and autophagy which may instigate tumorigenesis. It is not surprising therefore, that activation of canonical and non-canonical NF-κB pathways is increasingly recognized as an important driver of pancreatic injury, progression to tumorigenesis and drug resistance. Paradoxically, NF-κB dysregulation has also been shown to inhibit pancreatic inflammation and pancreatic cancer, depending on the context. A pro-oncogenic or pro-suppressive role for individual components of the NF-κB pathway appears to be cell type, microenvironment and even stage dependent. This review provides an outline of NF-κB signaling, focusing on the role of the various NF-κB family members in the evolving inflammatory PDAC microenvironment. Finally, we discuss pharmacological control of NF-κB to curb inflammation, focussing on novel anti-cancer agents which reinstate the process of cancer cell death, the Smac mimetics and their pre-clinical and early clinical trials.
    Language English
    Publishing date 2021-09-07
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2527080-1
    ISSN 2072-6694
    ISSN 2072-6694
    DOI 10.3390/cancers13184510
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: The Walrus and the Carpenter: Complex Regulation of Tumor Immunity in Colorectal Cancer.

    Dewson, Grant / Silke, John

    Cell

    2018  Volume 174, Issue 1, Page(s) 14–16

    Abstract: Immune infiltration has been correlated with survival of patients with colorectal cancer. In this issue, Ziegler et al. reveal complex and unexpected connections between loss of STAT3, mitophagy, and the induction of an adaptive immune response that ... ...

    Abstract Immune infiltration has been correlated with survival of patients with colorectal cancer. In this issue, Ziegler et al. reveal complex and unexpected connections between loss of STAT3, mitophagy, and the induction of an adaptive immune response that limits the growth of colorectal carcinoma.
    MeSH term(s) Adaptive Immunity ; Animals ; Carcinogenesis ; Colorectal Neoplasms ; Epithelial Cells ; Humans ; Mitochondrial Degradation ; STAT3 Transcription Factor ; Walruses
    Chemical Substances STAT3 Transcription Factor
    Language English
    Publishing date 2018-07-03
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Comment
    ZDB-ID 187009-9
    ISSN 1097-4172 ; 0092-8674
    ISSN (online) 1097-4172
    ISSN 0092-8674
    DOI 10.1016/j.cell.2018.06.009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: An overview of mammalian p38 mitogen-activated protein kinases, central regulators of cell stress and receptor signaling.

    Han, Jiahuai / Wu, Jianfeng / Silke, John

    F1000Research

    2020  Volume 9

    Abstract: The p38 family is a highly evolutionarily conserved group of mitogen-activated protein kinases (MAPKs) that is involved in and helps co-ordinate cellular responses to nearly all stressful stimuli. This review provides a succinct summary of multiple ... ...

    Abstract The p38 family is a highly evolutionarily conserved group of mitogen-activated protein kinases (MAPKs) that is involved in and helps co-ordinate cellular responses to nearly all stressful stimuli. This review provides a succinct summary of multiple aspects of the biology, role, and substrates of the mammalian family of p38 kinases. Since p38 activity is implicated in inflammatory and other diseases, we also discuss the clinical implications and pharmaceutical approaches to inhibit p38.
    MeSH term(s) Animals ; Enzyme Activation ; Signal Transduction ; Stress, Physiological ; p38 Mitogen-Activated Protein Kinases
    Chemical Substances p38 Mitogen-Activated Protein Kinases (EC 2.7.11.24)
    Language English
    Publishing date 2020-06-29
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2699932-8
    ISSN 2046-1402 ; 2046-1402
    ISSN (online) 2046-1402
    ISSN 2046-1402
    DOI 10.12688/f1000research.22092.1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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