Cellular senescence limits translational readthrough.
Ontology highlight
ABSTRACT: The origin and evolution of cancer cells is considered to be mainly fueled by DNA mutations. Although translation errors could also expand the cellular proteome, their role in cancer biology remains poorly understood. Tumor suppressors called caretakers block cancer initiation and progression by preventing DNA mutations and/or stimulating DNA repair. If translational errors contribute to tumorigenesis, then caretaker genes should prevent such errors in normal cells in response to oncogenic stimuli. Here, we show that the process of cellular senescence induced by oncogenes, tumor suppressors or chemotherapeutic drugs is associated with a reduction in translational readthrough (TR) measured using reporters containing termination codons withing the context of both normal translation terminati
SUBMITTER: Del Toro N
PROVIDER: S-EPMC8649927 | biostudies-literature | 2021 Dec
REPOSITORIES: biostudies-literature
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