The Cure VCP Scientific Conference 2021: Molecular and clinical insights into neurodegeneration and myopathy linked to multisystem proteinopathy-1 (MSP-1).

Amyotrophic lateral sclerosis Autophagy Clinical trial Frontotemporal dementia Inclusion body myopathy Inhibitor Motor neuron disease Paget's disease of the bone Proteinopathy Ubiquitin VCP p97

Journal

Neurobiology of disease
ISSN: 1095-953X
Titre abrégé: Neurobiol Dis
Pays: United States
ID NLM: 9500169

Informations de publication

Date de publication:
07 2022
Historique:
received: 26 01 2022
revised: 08 03 2022
accepted: 05 04 2022
pubmed: 12 4 2022
medline: 20 5 2022
entrez: 11 4 2022
Statut: ppublish

Résumé

The 2021 VCP Scientific Conference took place virtually from September 9-10, 2021. This conference, planned and organized by the nonprofit patient advocacy group Cure VCP Disease, Inc. (https://www.curevcp.org), was the first VCP focused meeting since the 215th ENMC International Workshop VCP-related multi-system proteinopathy in 2016 (Evangelista et al., 2016). Mutations in VCP cause a complex and heterogenous disease termed inclusion body myopathy (IBM) with Paget's disease of the bone (PDB) and frontotemporal dementia (FTD) (IBMPFD), or multisystem proteinopathy 1 (MSP-1) Kimonis (n.d.), Kovach et al. (2001), Kimonis et al. (2000). In addition, VCP mutations also cause other age-related neurodegenerative disorders including amyptrophic lateral sclerosis (ALS), Parkinsonism, Charcot-Marie type II-B, vacuolar tauopathy among others (Korb et al., 2022). The objectives of this conference were as follows: (1) to provide a forum that facilitates sharing of published and unpublished information on physiological roles of p97/VCP, and on how mutations of VCP lead to diseases; (2) to bolster understanding of mechanisms involved in p97/VCP-relevant diseases and to enable identification of therapeutics to treat these conditions; (3) to identify gaps and barriers of further discoveries and translational research in the p97/VCP field; (4) to set a concrete basic and translational research agenda for future studies including crucial discussions on biomarker discoveries and patient longitudinal studies to facilitate near-term clinical trials; (5) to accelerate cross-disciplinary research collaborations among p97/VCP researchers; (6) to enable attendees to learn about new tools and reagents with the potential to facilitate p97/VCP research; (7) to assist trainees in propelling their research and to foster mentorship from leaders in the field; and (8) to promote diversity and inclusion of under-represented minorities in p97/VCP research as diversity is critically important for strong scientific research. Given the range of topics, the VCP Scientific Conference brought together over one hundred and forty individuals representing a diverse group of research scientists, trainees, medical practitioners, industry representatives, and patient advocates. Twenty-five institutions with individuals from thirteen countries attended this virtual meeting. In this report, we summarize the major topics presented at this conference by a range of experts.

Identifiants

pubmed: 35405261
pii: S0969-9961(22)00114-0
doi: 10.1016/j.nbd.2022.105722
pmc: PMC9169230
mid: NIHMS1812088
pii:
doi:

Substances chimiques

Cell Cycle Proteins 0
Merozoite Surface Protein 1 0
VCP protein, human EC 3.6.4.6
Valosin Containing Protein EC 3.6.4.6

Types de publication

Journal Article Review Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

105722

Subventions

Organisme : NIGMS NIH HHS
ID : K12 GM133314
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM127557
Pays : United States
Organisme : NINDS NIH HHS
ID : R21 NS123631
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM133772
Pays : United States

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.

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Auteurs

Michelle A Johnson (MA)

Department of Developmental Molecular and Chemical Biology, Tufts University School of Medicine, Boston, MA, United States of America.

Jacob A Klickstein (JA)

Department of Developmental Molecular and Chemical Biology, Tufts University School of Medicine, Boston, MA, United States of America.

Richa Khanna (R)

Department of Developmental Molecular and Chemical Biology, Tufts University School of Medicine, Boston, MA, United States of America.

Yunzi Gou (Y)

Department of Pathology and Laboratory Medicine, University of California, Irvine, CA, United States of America.

Malavika Raman (M)

Department of Developmental Molecular and Chemical Biology, Tufts University School of Medicine, Boston, MA, United States of America. Electronic address: malavika.raman@tufts.edu.

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Classifications MeSH