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Identification of SYK inhibitor, R406 as a novel senolytic agent.


ABSTRACT: The selective removal of senescent cells by senolytics is suggested as a potential approach to reverse aging and extend lifespan. Using high-throughput screening with replicative senescence of human diploid fibroblasts (HDFs), we identified a novel senolytic drug R406 that showed selective toxicity in senescent cells. Using flow cytometry and caspase expression analysis, we confirmed that R406 caused apoptotic cell death along with morphological changes in senescent cells. Interestingly, R406 altered the cell survival-related molecular processes including the inhibition of phosphorylation of the focal adhesion kinase (FAK) and p38 mitogen-activated protein kinase (MAPK) in senescent cells. This pattern was not observed in other known senolytic agent ABT263. Correspondingly, apoptotic cell death in senescent cells was induced by simultaneously blocking the FAK and p38 pathways. Taken together, we suggest that R406 acts as a senolytic drug by inducing apoptosis and reducing cell attachment capacity.

SUBMITTER: Cho HJ 

PROVIDER: S-EPMC7244031 | biostudies-literature | 2020 May

REPOSITORIES: biostudies-literature

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Identification of SYK inhibitor, R406 as a novel senolytic agent.

Cho Hyun-Ji HJ   Yang Eun Jae EJ   Park Joon Tae JT   Kim Jae-Ryong JR   Kim Eok-Cheon EC   Jung Kyong-Jin KJ   Park Sang Chul SC   Lee Young-Sam YS  

Aging 20200507 9


The selective removal of senescent cells by senolytics is suggested as a potential approach to reverse aging and extend lifespan. Using high-throughput screening with replicative senescence of human diploid fibroblasts (HDFs), we identified a novel senolytic drug R406 that showed selective toxicity in senescent cells. Using flow cytometry and caspase expression analysis, we confirmed that R406 caused apoptotic cell death along with morphological changes in senescent cells. Interestingly, R406 al  ...[more]

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