UV-induced G4 DNA structures recruit ZRF1 which prevents UV-induced senescence.
Ontology highlight
ABSTRACT: Senescence has two roles in oncology: it is known as a potent tumor-suppressive mechanism, which also supports tissue regeneration and repair, it is also known to contribute to reduced patient resilience, which might lead to cancer recurrence and resistance after therapy. Senescence can be activated in a DNA damage-dependent and -independent manner. It is not clear which type of genomic lesions induces senescence, but it is known that UV irradiation can activate cellular senescence in photoaged skin. Proteins that support the repair of DNA damage are linked to senescence but how they contribute to senescence after UV irradiation is still unknown. Here, we unraveled a mechanism showing that upon UV irradiation multiple G-quadruplex (G4) DNA structures accumulate in cell nuclei, which leads
SUBMITTER: De Magis A
PROVIDER: S-EPMC10593929 | biostudies-literature | 2023 Oct
REPOSITORIES: biostudies-literature
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