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  1. Article ; Online: Editor Profile: Eric Chevet.

    Chevet, Eric

    The FEBS journal

    2022  Volume 289, Issue 22, Page(s) 6832–6834

    Abstract: In this special interview series, we profile members of The FEBS Journal Editorial Board to highlight their research focus, perspectives on the journal and future directions in their field. Eric Chevet is Research Director at the French National ... ...

    Abstract In this special interview series, we profile members of The FEBS Journal Editorial Board to highlight their research focus, perspectives on the journal and future directions in their field. Eric Chevet is Research Director at the French National Institute of Health (INSERM) and Director of the INSERM Unit U1242 'Oncogenesis, Stress, Signaling' in the Comprehensive Cancer Centre Eugène Marquis at the University of Rennes. He has served as Editorial Board Member of The FEBS Journal since 2019.
    Language English
    Publishing date 2022-03-25
    Publishing country England
    Document type Editorial
    ZDB-ID 2173655-8
    ISSN 1742-4658 ; 1742-464X
    ISSN (online) 1742-4658
    ISSN 1742-464X
    DOI 10.1111/febs.16428
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Editor Profile: Eric Chevet

    Chevet, Eric

    The FEBS Journal. 2022 Nov., v. 289, no. 22 p.6832-6834

    2022  

    Abstract: In this special interview series, we profile members of The FEBS Journal Editorial Board to highlight their research focus, perspectives on the journal and future directions in their field. Eric Chevet is Research Director at the French National ... ...

    Institution The FEBS Journal Editorial TeamThe FEBS Journal Editorial Office, Cambridge, UK
    Abstract In this special interview series, we profile members of The FEBS Journal Editorial Board to highlight their research focus, perspectives on the journal and future directions in their field. Eric Chevet is Research Director at the French National Institute of Health (INSERM) and Director of the INSERM Unit U1242 ‘Oncogenesis, Stress, Signaling’ in the Comprehensive Cancer Centre Eugène Marquis at the University of Rennes. He has served as Editorial Board Member of The FEBS Journal since 2019.
    Keywords National Institutes of Health ; carcinogenesis ; fields ; interviews ; journals ; neoplasms ; universities
    Language English
    Dates of publication 2022-11
    Size p. 6832-6834.
    Publishing place John Wiley & Sons, Ltd
    Document type Article ; Online
    Note EDITORIAL
    ZDB-ID 2173655-8
    ISSN 1742-4658 ; 1742-464X
    ISSN (online) 1742-4658
    ISSN 1742-464X
    DOI 10.1111/febs.16428
    Database NAL-Catalogue (AGRICOLA)

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  3. Article ; Online: American Journal of Physiology-Cell Physiology

    Chevet, Eric

    American journal of physiology. Cell physiology

    2019  Volume 317, Issue 5, Page(s) C867–C868

    MeSH term(s) Cell Physiological Phenomena ; Colonic Neoplasms ; Exosomes ; Humans ; United States
    Language English
    Publishing date 2019-09-18
    Publishing country United States
    Document type Editorial ; Research Support, Non-U.S. Gov't ; Comment
    ZDB-ID 392098-7
    ISSN 1522-1563 ; 0363-6143
    ISSN (online) 1522-1563
    ISSN 0363-6143
    DOI 10.1152/ajpcell.00379.2019
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  4. Article ; Online: Protein homeostasis imprinting across evolution.

    Koutsandreas, Thodoris / Felden, Brice / Chevet, Eric / Chatziioannou, Aristotelis

    NAR genomics and bioinformatics

    2024  Volume 6, Issue 1, Page(s) lqae014

    Abstract: Protein homeostasis (a.k.a. proteostasis) is associated with the primary functions of life, and therefore with evolution. However, it is unclear how cellular proteostasis machines have evolved to adjust protein biogenesis needs to environmental ... ...

    Abstract Protein homeostasis (a.k.a. proteostasis) is associated with the primary functions of life, and therefore with evolution. However, it is unclear how cellular proteostasis machines have evolved to adjust protein biogenesis needs to environmental constraints. Herein, we describe a novel computational approach, based on semantic network analysis, to evaluate proteostasis plasticity during evolution. We show that the molecular components of the proteostasis network (PN) are reliable metrics to deconvolute the life forms into Archaea, Bacteria and Eukarya and to assess the evolution rates among species. Semantic graphs were used as new criteria to evaluate PN complexity in 93 Eukarya, 250 Bacteria and 62 Archaea, thus representing a novel strategy for taxonomic classification, which provided information about species divergence. Kingdom-specific PN components were identified, suggesting that PN complexity may correlate with evolution. We found that the gains that occurred throughout PN evolution revealed a dichotomy within both the PN conserved modules and within kingdom-specific modules. Additionally, many of these components contribute to the evolutionary imprinting of other conserved mechanisms. Finally, the current study suggests a new way to exploit the genomic annotation of biomedical ontologies, deriving new knowledge from the semantic comparison of different biological systems.
    Language English
    Publishing date 2024-02-15
    Publishing country England
    Document type Journal Article
    ISSN 2631-9268
    ISSN (online) 2631-9268
    DOI 10.1093/nargab/lqae014
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: ER stress signaling at the interphase between MASH and hepatocellular carcinoma.

    Hazari, Younis / Chevet, Eric / Bailly-Maitre, Béatrice / Hetz, Claudio

    Hepatology (Baltimore, Md.)

    2024  

    Abstract: Hepato-cellular carcinoma (HCC) is the most frequent primary liver cancer with an extremely poor prognosis and often develops on preset of chronic liver diseases. Major risk factors for HCC include metabolic dysfunction-associated steatohepatitis (MASH), ...

    Abstract Hepato-cellular carcinoma (HCC) is the most frequent primary liver cancer with an extremely poor prognosis and often develops on preset of chronic liver diseases. Major risk factors for HCC include metabolic dysfunction-associated steatohepatitis (MASH), a complex multifactorial condition associated with abnormal endoplasmic reticulum (ER) proteostasis. To cope with ER stress, the unfolded protein response (UPR) engages adaptive reactions to restore the secretory capacity of the cell. Recent advances revealed that ER stress signaling plays a critical role in HCC progression. Here we propose that chronic ER stress is a common transversal factor contributing to the transition from liver disease (risk factor) to HCC. Interventional strategies to target the UPR in HCC as cancer therapy are also discussed.
    Language English
    Publishing date 2024-04-16
    Publishing country United States
    Document type Journal Article
    ZDB-ID 604603-4
    ISSN 1527-3350 ; 0270-9139
    ISSN (online) 1527-3350
    ISSN 0270-9139
    DOI 10.1097/HEP.0000000000000893
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  6. Article ; Online: Exploring the IRE1 interactome: From canonical signaling functions to unexpected roles.

    Le Goupil, Simon / Laprade, Hadrien / Aubry, Marc / Chevet, Eric

    The Journal of biological chemistry

    2024  Volume 300, Issue 4, Page(s) 107169

    Abstract: The unfolded protein response is a mechanism aiming at restoring endoplasmic reticulum (ER) homeostasis and is likely involved in other adaptive pathways. The unfolded protein response is transduced by three proteins acting as sensors and triggering ... ...

    Abstract The unfolded protein response is a mechanism aiming at restoring endoplasmic reticulum (ER) homeostasis and is likely involved in other adaptive pathways. The unfolded protein response is transduced by three proteins acting as sensors and triggering downstream signaling pathways. Among them, inositol-requiring enzyme 1 alpha (IRE1α) (referred to as IRE1 hereafter), an endoplasmic reticulum-resident type I transmembrane protein, exerts its function through both kinase and endoribonuclease activities, resulting in both X-box binding protein 1 mRNA splicing and RNA degradation (regulated ire1 dependent decay). An increasing number of studies have reported protein-protein interactions as regulators of these signaling mechanisms, and additionally, driving other noncanonical functions. In this review, we deliver evolutive and structural insights on IRE1 and further describe how this protein interaction network (interactome) regulates IRE1 signaling abilities or mediates other cellular processes through catalytic-independent mechanisms. Moreover, we focus on newly discovered targets of IRE1 kinase activity and discuss potentially novel IRE1 functions based on the nature of the interactome, thereby identifying new fields to explore regarding this protein's biological roles.
    MeSH term(s) Protein Serine-Threonine Kinases/metabolism ; Protein Serine-Threonine Kinases/genetics ; Humans ; Endoribonucleases/metabolism ; Endoribonucleases/genetics ; Signal Transduction ; Animals ; Unfolded Protein Response ; Endoplasmic Reticulum/metabolism ; Protein Interaction Maps
    Chemical Substances Protein Serine-Threonine Kinases (EC 2.7.11.1) ; Endoribonucleases (EC 3.1.-) ; ERN1 protein, human (EC 2.7.11.1)
    Language English
    Publishing date 2024-03-15
    Publishing country United States
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 2997-x
    ISSN 1083-351X ; 0021-9258
    ISSN (online) 1083-351X
    ISSN 0021-9258
    DOI 10.1016/j.jbc.2024.107169
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Introducing Emerging Methods and Technologies.

    Chevet, Eric / Breuer, Manuel

    The FEBS journal

    2021  Volume 288, Issue 16, Page(s) 4728–4729

    Abstract: With the current issue of The FEBS Journal, we are introducing a new category of invited review article contributions on Emerging Methods and Technologies. These articles provide an overview and discussion of recent, emerging methods that significantly ... ...

    Abstract With the current issue of The FEBS Journal, we are introducing a new category of invited review article contributions on Emerging Methods and Technologies. These articles provide an overview and discussion of recent, emerging methods that significantly advance and improve research efforts in the different fields of molecular and cellular research of our The FEBS Journal authors and readers. Deputy Editorial Manager Manuel Breuer and our Emerging Methods and Technologies Commissioning Editor Eric Chevet introduce the series.
    MeSH term(s) Autoimmune Diseases/immunology ; Humans ; Membrane Proteins/analysis ; Membrane Proteins/metabolism ; Neoplasms/immunology ; Neoplasms/therapy ; Polyethylene Terephthalates/metabolism ; Polysaccharides/chemistry ; Polysaccharides/immunology
    Chemical Substances Membrane Proteins ; Polyethylene Terephthalates ; Polysaccharides
    Language English
    Publishing date 2021-08-16
    Publishing country England
    Document type Editorial ; Introductory Journal Article
    ZDB-ID 2173655-8
    ISSN 1742-4658 ; 1742-464X
    ISSN (online) 1742-4658
    ISSN 1742-464X
    DOI 10.1111/febs.16144
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  8. Article: Introducing Emerging Methods and Technologies

    Chevet, Eric / Breuer, Manuel

    FEBS journal. 2021 Aug., v. 288, no. 16

    2021  

    Abstract: With the current issue of The FEBS Journal, we are introducing a new category of invited review article contributions on Emerging Methods and Technologies. These articles provide an overview and discussion of recent, emerging methods that significantly ... ...

    Abstract With the current issue of The FEBS Journal, we are introducing a new category of invited review article contributions on Emerging Methods and Technologies. These articles provide an overview and discussion of recent, emerging methods that significantly advance and improve research efforts in the different fields of molecular and cellular research of our The FEBS Journal authors and readers. Deputy Editorial Manager Manuel Breuer and our Emerging Methods and Technologies Commissioning Editor Eric Chevet introduce the series.
    Keywords journals ; managers ; technology
    Language English
    Dates of publication 2021-08
    Size p. 4728-4729.
    Publishing place John Wiley & Sons, Ltd
    Document type Article
    Note EDITORIAL
    ZDB-ID 2173655-8
    ISSN 1742-4658 ; 1742-464X
    ISSN (online) 1742-4658
    ISSN 1742-464X
    DOI 10.1111/febs.16144
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  9. Article ; Online: Dynamic tandem proximity-based proteomics-Protein trafficking at the proteome-scale.

    Chevet, Eric / De Matteis, Maria Antonietta / Eskelinen, Eeva-Liisa / Farhan, Hesso

    Traffic (Copenhagen, Denmark)

    2023  Volume 24, Issue 11, Page(s) 546–548

    Abstract: TransitID is a new methodology based on proximity labeling allowing for the study of protein trafficking a the proteome scale. ...

    Abstract TransitID is a new methodology based on proximity labeling allowing for the study of protein trafficking a the proteome scale.
    MeSH term(s) Proteome/metabolism ; Proteomics/methods ; Protein Transport
    Chemical Substances Proteome
    Language English
    Publishing date 2023-08-15
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1483852-7
    ISSN 1600-0854 ; 1398-9219
    ISSN (online) 1600-0854
    ISSN 1398-9219
    DOI 10.1111/tra.12914
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  10. Article ; Online: A TRAFFIC themed series - Host membrane trafficking subversion by pathogens.

    Chevet, Eric / De Matteis, Maria Antonietta / Eskelinen, Eeva-Liisa / Farhan, Hesso

    Traffic (Copenhagen, Denmark)

    2023  Volume 24, Issue 3, Page(s) 112–113

    Language English
    Publishing date 2023-02-03
    Publishing country England
    Document type Editorial
    ZDB-ID 1483852-7
    ISSN 1600-0854 ; 1398-9219
    ISSN (online) 1600-0854
    ISSN 1398-9219
    DOI 10.1111/tra.12882
    Database MEDical Literature Analysis and Retrieval System OnLINE

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