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Discovery of senolytics using machine learning.
Smer-Barreto, Vanessa; Quintanilla, Andrea; Elliott, Richard J R; Dawson, John C; Sun, Jiugeng; Campa, Víctor M; Lorente-Macías, Álvaro; Unciti-Broceta, Asier; Carragher, Neil O; Acosta, Juan Carlos; Oyarzún, Diego A.
Afiliação
  • Smer-Barreto V; Cancer Research UK Edinburgh Centre, MRC Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, EH4 2XR, UK. vanessa.smerbarreto@ed.ac.uk.
  • Quintanilla A; Instituto de Biomedicina y Biotecnología de Cantabria (IBBTEC), CSIC-Universidad de Cantabria-SODERCAN. C/ Albert Einstein 22, Santander, 39011, Spain.
  • Elliott RJR; Cancer Research UK Edinburgh Centre, MRC Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, EH4 2XR, UK.
  • Dawson JC; Cancer Research UK Edinburgh Centre, MRC Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, EH4 2XR, UK.
  • Sun J; School of Informatics, University of Edinburgh, 10 Crichton St, Edinburgh, EH8 9AB, UK.
  • Campa VM; Instituto de Biomedicina y Biotecnología de Cantabria (IBBTEC), CSIC-Universidad de Cantabria-SODERCAN. C/ Albert Einstein 22, Santander, 39011, Spain.
  • Lorente-Macías Á; Cancer Research UK Edinburgh Centre, MRC Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, EH4 2XR, UK.
  • Unciti-Broceta A; Cancer Research UK Edinburgh Centre, MRC Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, EH4 2XR, UK.
  • Carragher NO; Cancer Research UK Edinburgh Centre, MRC Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, EH4 2XR, UK.
  • Acosta JC; Cancer Research UK Edinburgh Centre, MRC Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, EH4 2XR, UK. juan.acosta@unican.es.
  • Oyarzún DA; Instituto de Biomedicina y Biotecnología de Cantabria (IBBTEC), CSIC-Universidad de Cantabria-SODERCAN. C/ Albert Einstein 22, Santander, 39011, Spain. juan.acosta@unican.es.
Nat Commun ; 14(1): 3445, 2023 06 10.
Article em En | MEDLINE | ID: mdl-37301862
ABSTRACT
Cellular senescence is a stress response involved in ageing and diverse disease processes including cancer, type-2 diabetes, osteoarthritis and viral infection. Despite growing interest in targeted elimination of senescent cells, only few senolytics are known due to the lack of well-characterised molecular targets. Here, we report the discovery of three senolytics using cost-effective machine learning algorithms trained solely on published data. We computationally screened various chemical libraries and validated the senolytic action of ginkgetin, periplocin and oleandrin in human cell lines under various modalities of senescence. The compounds have potency comparable to known senolytics, and we show that oleandrin has improved potency over its target as compared to best-in-class alternatives. Our approach led to several hundred-fold reduction in drug screening costs and demonstrates that artificial intelligence can take maximum advantage of small and heterogeneous drug screening data, paving the way for new open science approaches to early-stage drug discovery.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Inteligência Artificial / Senoterapia Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Inteligência Artificial / Senoterapia Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article