2023
DOI: 10.1016/j.bbrc.2023.04.113
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TOPK inhibits TNF-α-induced granulosa cell apoptosis via regulation of SIRT1/p53

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Cited by 5 publications
(2 citation statements)
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“…Interferons exert an anticancer function; for instance, IFNα induces tumor cell death via the Fas pathway and is successfully used as a tumor immunotherapy ( Kimura et al, 2003 ). In general, tumor necrosis factors (TNFs) suppress P53 function and facilitate cell apoptosis ( Joo et al, 2023 ). In addition, colony-stimulating proteins, such as CSF-1 and their receptors, increase tumor cell proliferation and survival in an autocrine or paracrine manner ( Achkova & Maher, 2016 ).…”
Section: Introductionmentioning
confidence: 99%
“…Interferons exert an anticancer function; for instance, IFNα induces tumor cell death via the Fas pathway and is successfully used as a tumor immunotherapy ( Kimura et al, 2003 ). In general, tumor necrosis factors (TNFs) suppress P53 function and facilitate cell apoptosis ( Joo et al, 2023 ). In addition, colony-stimulating proteins, such as CSF-1 and their receptors, increase tumor cell proliferation and survival in an autocrine or paracrine manner ( Achkova & Maher, 2016 ).…”
Section: Introductionmentioning
confidence: 99%
“…The DLX1, P53, and β-catenin are the key factors in cell apoptosis pathways, and overexpressions of DLX1, NF-κB, and β-catenin inhibit cell apoptosis and promote cell proliferation [8] . TNF-α and P53 promote cell apoptosis and inhibit cell proliferation [9] . Our results showed that DLX1, NF-κB, and β-catenin in the TUG1-OE group were significantly higher than those in the control group, and TNF-α and P53 expressions were significantly lower than those in the control group ( P <0.01).…”
mentioning
confidence: 99%