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1.
Drug Discov Today ; 26(11): 2489-2495, 2021 11.
Artigo em Inglês | MEDLINE | ID: mdl-34015541

RESUMO

Spiralling research costs combined with urgent pressures from the Coronavirus 2019 (COVID-19) pandemic and the consequences of climate disruption are forcing changes in drug discovery. Increasing the predictive power of in vitro human assays and using them earlier in discovery would refocus resources on more successful research strategies and reduce animal studies. Increasing laboratory automation enables effective social distancing for researchers, while allowing integrated data capture from remote laboratory networks. Such disruptive changes would not only enable more cost-effective drug discovery, but could also reduce the overall carbon footprint of discovering new drugs.


Assuntos
Inteligência Artificial , COVID-19 , Mudança Climática , Tecnologia Disruptiva , Descoberta de Drogas , Automação , Pegada de Carbono , Comportamento Cooperativo , Confiabilidade dos Dados , Humanos , Técnicas In Vitro , Aprendizado de Máquina , Distanciamento Físico , SARS-CoV-2
2.
Drug Discov Today ; 22(2): 327-339, 2017 02.
Artigo em Inglês | MEDLINE | ID: mdl-27989722

RESUMO

Decades of costly failures in translating drug candidates from preclinical disease models to human therapeutic use warrant reconsideration of the priority placed on animal models in biomedical research. Following an international workshop attended by experts from academia, government institutions, research funding bodies, and the corporate and non-governmental organisation (NGO) sectors, in this consensus report, we analyse, as case studies, five disease areas with major unmet needs for new treatments. In view of the scientifically driven transition towards a human pathways-based paradigm in toxicology, a similar paradigm shift appears to be justified in biomedical research. There is a pressing need for an approach that strategically implements advanced, human biology-based models and tools to understand disease pathways at multiple biological scales. We present recommendations to help achieve this.


Assuntos
Pesquisa Biomédica , Descoberta de Drogas , Doença de Alzheimer , Animais , Asma , Transtorno do Espectro Autista , Doenças Autoimunes , Consenso , Fibrose Cística , Humanos , Hepatopatias , Modelos Animais
3.
Oncotarget ; 7(26): 38999-39016, 2016 Jun 28.
Artigo em Inglês | MEDLINE | ID: mdl-27229915

RESUMO

Much of Alzheimer disease (AD) research has been traditionally based on the use of animals, which have been extensively applied in an effort to both improve our understanding of the pathophysiological mechanisms of the disease and to test novel therapeutic approaches. However, decades of such research have not effectively translated into substantial therapeutic success for human patients. Here we critically discuss these issues in order to determine how existing human-based methods can be applied to study AD pathology and develop novel therapeutics. These methods, which include patient-derived cells, computational analysis and models, together with large-scale epidemiological studies represent novel and exciting tools to enhance and forward AD research. In particular, these methods are helping advance AD research by contributing multifactorial and multidimensional perspectives, especially considering the crucial role played by lifestyle risk factors in the determination of AD risk. In addition to research techniques, we also consider related pitfalls and flaws in the current research funding system. Conversely, we identify encouraging new trends in research and government policy. In light of these new research directions, we provide recommendations regarding prioritization of research funding. The goal of this document is to stimulate scientific and public discussion on the need to explore new avenues in AD research, considering outcome and ethics as core principles to reliably judge traditional research efforts and eventually undertake new research strategies.


Assuntos
Doença de Alzheimer/genética , Doença de Alzheimer/terapia , Pesquisa Biomédica/tendências , Doença de Alzheimer/metabolismo , Animais , Simulação por Computador , Modelos Animais de Doenças , Humanos , Células-Tronco Pluripotentes Induzidas/citologia , National Institutes of Health (U.S.) , Neuroimagem , Projetos de Pesquisa , Apoio à Pesquisa como Assunto , Fatores de Risco , Estados Unidos
4.
Drug Discov Today ; 19(8): 1114-24, 2014 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-24662035

RESUMO

Using Alzheimer's disease as a case study, this review argues that it might be time to consider a new paradigm in medical research and drug discovery. The existing framework is overly dependent on often unvalidated animal models, particularly transgenic mice. Translational success remains elusive and costly late-stage drug failure is common. The conventional paradigm tends to overlook species differences and assumes that animal-based findings are generally applicable to humans. Could pathways-based research using advanced human-specific models probed with new tools, including those of systems biology, take centre stage? The current transition in chemical toxicology to a 21st-century paradigm could be a model for health research, with probable medical and economic benefits.


Assuntos
Doença de Alzheimer/tratamento farmacológico , Descoberta de Drogas/métodos , Animais , Modelos Animais de Doenças , Humanos , Pesquisa , Biologia de Sistemas/métodos
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