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LSD1/PRMT6-targeting gene therapy to attenuate androgen receptor toxic gain-of-function ameliorates spinobulbar muscular atrophy phenotypes in flies and mice

Abstract:
The workshop held in the Netherlands from October 20–22, 2023, united 27 scientists from academia, healthcare, and industry representing 11 countries, alongside four patient and charity representatives. Focused on Kennedy's Disease (KD), also known as spinal and bulbar muscular atrophy (SBMA), the workshop aimed to consolidate knowledge, align on clinical trial designs, and promote participative medicine for effective treatments. Discussions emphasized KD's molecular mechanisms, highlighting its status as a neuromuscular disorder with motor neuron degeneration. Strategies for therapeutic intervention, including AR activity modulation and targeting post-translational modifications, were proposed. The need for diagnostic, prognostic, and target engagement biomarkers was stressed. Challenges in patient stratification and clinical trial recruitment were acknowledged, with the International KD/SBMA Registry praised for its role. The workshop concluded with a patient-focused session, underscoring challenges in KD diagnosis and the vital support provided by patient associations
Publication status:
Published
Peer review status:
Peer reviewed

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Role:
Author
ORCID:
0000-0003-0248-7580
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Role:
Author
ORCID:
0000-0003-3873-1258
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Role:
Author
ORCID:
0000-0002-2814-2743
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Role:
Author
ORCID:
0000-0001-8978-7206
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Role:
Author
ORCID:
0000-0002-9760-7655


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Funder identifier:
10.13039/501100002426
Grant:
GGP19128


Publisher:
Nature Research
Journal:
Nature Communications More from this journal
Volume:
14
Issue:
1
Pages:
603-603
Article number:
603
Publication date:
2023-02-06
DOI:
EISSN:
2041-1723
ISSN:
2041-1723


Language:
English
Keywords:
Pubs id:
1327704
Local pid:
pubs:1327704
Source identifiers:
W4319298561
Deposit date:
2026-05-01
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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