Correlation Engine 2.0
Clear Search sequence regions


  • adult (1)
  • brain tumour (1)
  • cohort (1)
  • female (1)
  • humans (1)
  • plasma (1)
  • reticulum (2)
  • ritonavir (10)
  • tumour (1)
  • xenograft (2)
  • Sizes of these terms reflect their relevance to your search.

    The protease inhibitor ritonavir (RTV) is a clinical-stage inhibitor of the human immunodeficiency virus. In a drug repositioning approach, we here exhibit the additional potential of RTV to augment current treatment of glioblastoma, the most aggressive primary brain tumour of adulthood. We explored the antitumour activity of RTV and mechanisms of action in a broad spectrum of short-term expanded clinical cell samples from primary and recurrent glioblastoma and in a cohort of conventional cell lines and non-tumour human neural controls in vitro. To validate RTV efficacy in monotherapeutic and in combinatorial settings, we used patient-derived xenograft models in a series of in vivo studies. RTV monotherapy induced a selective antineoplastic response and demonstrated cytostatic and anti-migratory activity at clinical plasma peak levels. Additional exposure to temozolomide or irradiation further enhanced the effects synergistically, fostered by mechanisms of autophagy and increased endoplasmic reticulum stress. In xenograft models, we consequently observed increasing overall survival under the combinatorial effect of RTV and temozolomide. Our data establish RTV as a valuable repositioning candidate for further exploration as an adjunct therapeutic in the clinical care of glioblastoma. Copyright © 2020 Elsevier Ltd. All rights reserved.

    Citation

    Laurèl Rauschenbach, Anja Wieland, Roman Reinartz, Sied Kebir, Andreas Till, Marvin Darkwah Oppong, Celia Dobersalske, Vivien Ullrich, Ashar Ahmad, Ramazan Jabbarli, Daniela Pierscianek, Holger Fröhlich, Matthias Simon, Oliver Brüstle, Ulrich Sure, Martin Glas, Björn Scheffler. Drug repositioning of antiretroviral ritonavir for combinatorial therapy in glioblastoma. European journal of cancer (Oxford, England : 1990). 2020 Nov;140:130-139

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 33091717

    View Full Text