Diosgenin, a naturally occurring steroid, suppresses fatty acid synthase expression in HER2‐overexpressing breast cancer cells through modulating Akt, mTOR and JNK phosphorylation

FEBS Letters
2007.0

Abstract

<jats:p>Fatty acid synthase (FAS) expression is markedly elevated in HER2‐overexpressing breast cancer cells. In this study, diosgenin, a plant‐derived steroid, was found to be effective in suppressing FAS expression in HER2‐overexpressing breast cancer cells. Diosgenin preferentially inhibited proliferation and induced apoptosis in HER2‐overexpressing cancer cells. Furthermore, diosgenin inhibited the phosphorylation of Akt and mTOR, and enhanced phosphorylation of JNK. The use of pharmacological inhibitors revealed that the modulation of Akt, mTOR and JNK phosphorylation was required for diosgenin‐induced FAS suppression. Finally, we showed that diosgenin could enhance paclitaxel‐induced cytotoxicity in HER2‐overexpressing cancer cells. These results suggested that diosgenin has the potential to advance as chemopreventive or chemotherapeutic agent for cancers that overexpress HER2.

Knowledge Graph

Similar Paper

Diosgenin, a naturally occurring steroid, suppresses fatty acid synthase expression in HER2‐overexpressing breast cancer cells through modulating Akt, mTOR and JNK phosphorylation
FEBS Letters 2007.0
Diosgenin, a naturally occurring furostanol saponin suppresses 3-hydroxy-3-methylglutaryl CoA reductase expression and induces apoptosis in HCT-116 human colon carcinoma cells
Cancer Letters 2007.0
Diosgenin Derivatives as Potential Antitumor Agents: Synthesis, Cytotoxicity, and Mechanism of Action
Journal of Natural Products 2021.0
Synthesis and cytotoxic activity of diosgenyl saponin analogues
Bioorganic &amp; Medicinal Chemistry 2008.0
Design and synthesis of diosgenin derivatives as apoptosis inducers through mitochondria-related pathways
European Journal of Medicinal Chemistry 2021.0
Structural analogues of diosgenyl saponins: Synthesis and anticancer activity
Bioorganic &amp; Medicinal Chemistry 2009.0
Novel diosgenin derivatives containing 1,3,4-oxadiazole/thiadiazole moieties as potential antitumor agents: Design, synthesis and cytotoxic evaluation
European Journal of Medicinal Chemistry 2020.0
Syntheses and structure–activity relationship studies of N-substituted-β-d-glucosaminides as selective cytotoxic agents
Bioorganic &amp; Medicinal Chemistry Letters 2012.0
Galloyl esters of trans-stilbenes are inhibitors of FASN with anticancer activity on non-small cell lung cancer cells
European Journal of Medicinal Chemistry 2019.0
Synthesis and cytotoxic effect of pseudodiosgenyl saponins with thio-ring F
Bioorganic &amp; Medicinal Chemistry Letters 2014.0