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Time-of-day effects of cancer drugs revealed by high-throughput deep phenotyping.
Ector, Carolin; Schmal, Christoph; Didier, Jeff; De Landtsheer, Sébastien; Finger, Anna-Marie; Müller-Marquardt, Francesca; Schulte, Johannes H; Sauter, Thomas; Keilholz, Ulrich; Herzel, Hanspeter; Kramer, Achim; Granada, Adrián E.
Afiliación
  • Ector C; Charité Comprehensive Cancer Center, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Schmal C; Faculty of Life Sciences, Humboldt-Universität zu Berlin, Berlin, Germany.
  • Didier J; Institute for Theoretical Biology, Humboldt-Universität zu Berlin, Berlin, Germany.
  • De Landtsheer S; Department of Life Sciences and Medicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.
  • Finger AM; Department of Life Sciences and Medicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.
  • Müller-Marquardt F; Institute for Medical Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Schulte JH; Department of Anatomy, University of California, San Francisco, San Francisco, CA, USA.
  • Sauter T; Charité Comprehensive Cancer Center, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Keilholz U; Institute of Research for Development, University of Montpellier, Montpellier, France.
  • Herzel H; Department of Pediatric Oncology, Hematology and Stem Cell Transplantation, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Kramer A; Clinic for Pediatrics and Adolescent Medicine, Universitätsklinikum Tübingen, Tübingen, Germany.
  • Granada AE; Department of Life Sciences and Medicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.
Nat Commun ; 15(1): 7205, 2024 Aug 22.
Article en En | MEDLINE | ID: mdl-39169017
ABSTRACT
The circadian clock, a fundamental biological regulator, governs essential cellular processes in health and disease. Circadian-based therapeutic strategies are increasingly gaining recognition as promising avenues. Aligning drug administration with the circadian rhythm can enhance treatment efficacy and minimize side effects. Yet, uncovering the optimal treatment timings remains challenging, limiting their widespread adoption. In this work, we introduce a high-throughput approach integrating live-imaging and data analysis techniques to deep-phenotype cancer cell models, evaluating their circadian rhythms, growth, and drug responses. We devise a streamlined process for profiling drug sensitivities across different times of the day, identifying optimal treatment windows and responsive cell types and drug combinations. Finally, we implement multiple computational tools to uncover cellular and genetic factors shaping time-of-day drug sensitivity. Our versatile approach is adaptable to various biological models, facilitating its broad application and relevance. Ultimately, this research leverages circadian rhythms to optimize anti-cancer drug treatments, promising improved outcomes and transformative treatment strategies.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fenotipo / Ritmo Circadiano / Neoplasias / Antineoplásicos Límite: Humans Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2024 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fenotipo / Ritmo Circadiano / Neoplasias / Antineoplásicos Límite: Humans Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2024 Tipo del documento: Article País de afiliación: Alemania