Mathematical modeling of ribosome competition informs testable treatment strategies for drug-tolerant cancer persister cells
Year: 2026
Type: article
Abstract: Systemic therapies for advanced cancers often induce initial responses but rarely achieve durable cures due to acquired resistance. Drug-tolerant persister (DTP) cells survive treatment without additional genetic mutations. We previously showed that melanoma DTP cells globally suppress mRNA translation while selectively maintaining translation of specific mRNAs, but the basis of this selectivity remained unclear. Here, we integrate stochastic modeling with experimental analyses to define the principles governing selective translation in DTP cells. We identify translational reprogramming as a conserved feature of DTP cells across cancer types and treatments. Reduced MYC-dependent ribosome biogenesis limits ribosome availability, creating a translational bottleneck. Modeling reveals that ribosome scarcity drives competition among mRNAs, thereby shaping selective translation. This framework uncovers a ribosome-dependent survival checkpoint in DTP cells and highlights ribosome thresholds as a potential vulnerability for overcoming therapy resistance.
Source: iScience
Institutions: Sichuan University, West China Medical Center of Sichuan University, West China Hospital of Sichuan University, Centre National de la Recherche Scientifique, Université Paris Cité, Sorbonne Université, Inserm, Université Côte d'Azur, Centre Méditerranéen de Médecine Moléculaire, State Key Laboratory of Biotherapy, Université Paris-Saclay, Institut Gustave Roussy, Institut national de recherche en sciences et technologies du numérique, Laboratoire Jacques-Louis Lions
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $3,240
OpenAlex ID: W7141400902
