Evidence map›Paper›PMID 38605409›Full record

ReviewMolecular brain2024

The 37TrillionCells initiative for improving global healthcare via cell-based interception and precision medicine: focus on neurodegenerative diseases.

Benoit Coulombe, Thomas M Durcan, Geneviève Bernard, Asmae Moursli, Christian Poitras, Denis Faubert, Maxime Pinard

Abstract readReview
In one paragraph

Review in Molecular brain, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Benoit CoulombeTranslational Proteomics Laboratory, Institut de Recherches Cliniques de Montréal, Montreal, QC, H2W 1R7, Canada. benoit.coulombe@ircm.qc.ca.ORCID 0000-0003-1702-0692
Thomas M DurcanThe Neuro's Early Drug Discovery Unit (EDDU), McGill University, Montreal, Canada.
Geneviève BernardDepartments of Neurology and Neurosurgery, Pediatrics and Human Genetics, McGill University, Montreal, Canada.
Asmae MoursliTranslational Proteomics Laboratory, Institut de Recherches Cliniques de Montréal, Montreal, QC, H2W 1R7, Canada.
Christian PoitrasTranslational Proteomics Laboratory, Institut de Recherches Cliniques de Montréal, Montreal, QC, H2W 1R7, Canada.
Denis FaubertMass Spectrometry and Proteomics Platform, Institut de Recherches Cliniques de Montréal, Montreal, QC, H2W1R7, Canada.
Maxime PinardTranslational Proteomics Laboratory, Institut de Recherches Cliniques de Montréal, Montreal, QC, H2W 1R7, Canada.

Funding

CIHR New investigator salary awardCIHR PJT-169095
6 · The paper itself

Abstract

One of the main burdens in the treatment of diseases is imputable to the delay between the appearance of molecular dysfunctions in the first affected disease cells and their presence in sufficient number for detection in specific tissues or organs. This delay obviously plays in favor of disease progression to an extent that makes efficient treatments difficult, as they arrive too late. The development of a novel medical strategy, termed cell-based interception and precision medicine, seeks to identify dysfunctional cells early, when tissue damages are not apparent and symptoms not yet present, and develop therapies to treat diseases early. Central to this strategy is the use of single-cell technologies that allow detection of molecular changes in cells at the time of phenotypical bifurcation from health to disease. In this article we describe a general procedure to support such an approach applied to neurodegenerative disorders. This procedure combines four components directed towards highly complementary objectives: 1) a high-performance single-cell proteomics (SCP) method (Detect), 2) the development of disease experimental cell models and predictive computational models of cell trajectories (Understand), 3) the discovery of specific targets and personalized therapies (Cure), and 4) the creation of a community of collaborating laboratories to accelerate the development of this novel medical paradigm (Collaborate). A global initiative named 37TrillionCells (37TC) was launched to advance the development of cell-based interception and precision medicine.

Indexed as

Neurodegenerative DiseasesDelivery of Health CareHumansPrecision MedicineProteomics37TrillionCellsCell-based interception and precision medicineiPSCLeukodystrophyOrganoidPOLR3-HLDSCoPE2-MSSingle-cell proteomics

Identifiers

PMID38605409
PMCPMC11007934

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.