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

IF 3.3 3区 医学 Q2 NEUROSCIENCES Molecular Brain Pub Date : 2024-04-11 DOI:10.1186/s13041-024-01088-4
Benoit Coulombe, Thomas M. Durcan, Geneviève Bernard, Asmae Moursli, Christian Poitras, Denis Faubert, Maxime Pinard
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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.
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通过细胞截获和精准医疗改善全球医疗保健的 37TrillionCells 计划:关注神经退行性疾病
治疗疾病的主要负担之一是,从最初受影响的疾病细胞出现分子功能障碍到它们在特定组织或器官中出现足够的数量以供检测之间的延迟。这种延迟显然有利于疾病的发展,使有效的治疗变得困难,因为它们来得太晚了。一种被称为细胞拦截和精准医疗的新型医疗策略的开发,旨在及早发现组织损伤不明显、症状尚未出现的功能失调细胞,并开发早期治疗疾病的疗法。这一战略的核心是利用单细胞技术,在细胞从健康到疾病的表型分叉期检测细胞的分子变化。在这篇文章中,我们介绍了支持这种方法应用于神经退行性疾病的一般程序。该程序由四个部分组成,目标高度互补:1)高性能单细胞蛋白质组学(SCP)方法(Detect);2)疾病实验细胞模型和细胞轨迹预测计算模型的开发(Understand);3)特定靶点和个性化疗法的发现(Cure);4)合作实验室社区的建立,以加速这种新型医学模式的发展(Collaborate)。一项名为 "37TrillionCells(37TC)"的全球倡议已经启动,以推动基于细胞的截获和精准医疗的发展。
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来源期刊
Molecular Brain
Molecular Brain NEUROSCIENCES-
CiteScore
7.30
自引率
0.00%
发文量
97
审稿时长
>12 weeks
期刊介绍: Molecular Brain is an open access, peer-reviewed journal that considers manuscripts on all aspects of studies on the nervous system at the molecular, cellular, and systems level providing a forum for scientists to communicate their findings. Molecular brain research is a rapidly expanding research field in which integrative approaches at the genetic, molecular, cellular and synaptic levels yield key information about the physiological and pathological brain. These studies involve the use of a wide range of modern techniques in molecular biology, genomics, proteomics, imaging and electrophysiology.
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