2012
DOI: 10.1055/s-0031-1295979
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Selective induction of apoptosis by HMG-CoA-reductase inhibitors in hepatoma cells is dependent on p53 expression

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“…198 199 This effect was achieved by inhibiting the oncoproteins, Skp2, and the signal transducer and activator of transcription 3, while upregulating AMP-associated protein kinase, which modulates metabolic homeostasis and suppresses tumor cell proliferation. 198 200 201 Alternatively, statin targets Notch gene family by upregulating Notch1, the primary signaling receptor responsible for the regulation of proteolysis, which in turn regulates tumor growth via an Akt-dependent signaling pathway. 202 203 Regulation of Akt pathway in HCC and statin use is not new; statin inhibits Akt and YAP signaling cascade, both of which are involved in hepatic fibrogenesis and carcinogenesis, through stabilization of r etinoid X r eceptor-α, a known antiproliferative chemotherapeutic target.…”
Section: Statin and Hepatocellular Carcinomamentioning
confidence: 99%
“…198 199 This effect was achieved by inhibiting the oncoproteins, Skp2, and the signal transducer and activator of transcription 3, while upregulating AMP-associated protein kinase, which modulates metabolic homeostasis and suppresses tumor cell proliferation. 198 200 201 Alternatively, statin targets Notch gene family by upregulating Notch1, the primary signaling receptor responsible for the regulation of proteolysis, which in turn regulates tumor growth via an Akt-dependent signaling pathway. 202 203 Regulation of Akt pathway in HCC and statin use is not new; statin inhibits Akt and YAP signaling cascade, both of which are involved in hepatic fibrogenesis and carcinogenesis, through stabilization of r etinoid X r eceptor-α, a known antiproliferative chemotherapeutic target.…”
Section: Statin and Hepatocellular Carcinomamentioning
confidence: 99%