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RNA seq on NEO2734, CFI-400945 or SASP treated cells

ABSTRACT: Senolytics, drugs that kill senescent cells, have been proposed to improve the response to pro-senescence cancer therapies. However, lack of broadly acting senolytic drugs remains a challenge. Using inducible CRISPR/Cas9-based genetic screens in different senescent cancer cell models, we identify here loss of the death receptor inhibitor cFLIP as a universal vulnerability of senescent cancer cells. Senescent cancer cells are primed for apoptotic death by NF-kB-mediated upregulation of death receptor DR5 and its ligand TRAIL but are protected from death by increased cFLIP. Activation of DR5 signaling by agonistic antibody, which can be enhanced further by suppression of cFLIP by BRD2 inhibition, leads to efficient killing of all senescent cancer cells tested. We validate this ?one-two punch? cancer therapy by combining pro-senescence therapy with DR5 activation in different animal models.

ORGANISM(S): Homo sapiens

PROVIDER: GSE191255 | GEO | 2022/08/24

REPOSITORIES: GEO

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Proteomic and biological analysis of metformin senomorphics effects on the mesenchymal stromal cells

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2022-02-15 | PXD028349 | Pride

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