Anemoside B4 exerts anti-cancer effect by inducing apoptosis and autophagy through inhibiton of PI3K/Akt/mTOR pathway in hepatocellular carcinoma
Identifieur interne : 000A89 ( Main/Exploration ); précédent : 000A88; suivant : 000A90Anemoside B4 exerts anti-cancer effect by inducing apoptosis and autophagy through inhibiton of PI3K/Akt/mTOR pathway in hepatocellular carcinoma
Auteurs : Shuyi Xue [République populaire de Chine] ; Yu Zhou [République populaire de Chine] ; Jin Zhang [République populaire de Chine] ; Zhuo Xiang [République populaire de Chine] ; Yang Liu [République populaire de Chine] ; Ting Miao [République populaire de Chine] ; Guoxin Liu [République populaire de Chine] ; Bangguo Liu [République populaire de Chine] ; Xu Liu [République populaire de Chine] ; Lixia Shen [République populaire de Chine] ; Zhe Zhang [République populaire de Chine] ; Mingchun Li [République populaire de Chine] ; Qing Miao [République populaire de Chine]Source :
- American Journal of Translational Research [ 1943-8141 ] ; 2019.
Abstract
Hepatocellular carcinoma (HCC) is a leading cause of cancer-related mortality worldwide and novel therapeutic approaches are urgently required. Anemoside B4 (AB4) is a compound extracted from
Url:
PubMed: 31105864
PubMed Central: 6511782
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Pmc, to step Corpus: 000352
- to stream Pmc, to step Curation: 000352
- to stream Pmc, to step Checkpoint: 000A15
- to stream Ncbi, to step Merge: 000631
- to stream Ncbi, to step Curation: 000631
- to stream Ncbi, to step Checkpoint: 000631
- to stream Main, to step Merge: 000A89
- to stream Main, to step Curation: 000A89
Le document en format XML
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<author><name sortKey="Miao, Ting" sort="Miao, Ting" uniqKey="Miao T" first="Ting" last="Miao">Ting Miao</name>
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<front><div type="abstract" xml:lang="en"><p>Hepatocellular carcinoma (HCC) is a leading cause of cancer-related mortality worldwide and novel therapeutic approaches are urgently required. Anemoside B4 (AB4) is a compound extracted from <italic>Pulsatilla chinensis</italic>
(<italic>P. chinensis</italic>
). Previous studies have indicated that <italic>P. chinensis</italic>
extract <italic>P. chinensis</italic>
saponins has anti-cancer activity. However, the pharmacological effect of AB4 in cancer is largely unknown. In this study, we investigated the anti-cancer efficacy of AB4 in HCC. We used CCK-8 assay and colony formation assay to evaluate the cytotoxicity of AB4 and found that this agent markedly inhibited SMMC7721 cell proliferation. By using a panel of morphological and molecular experiments, we reported that AB4 induced HCC SMMC7721 cell apoptosis and autophagy. Notably, AB4 treatment acts on the Bcl-2-caspase-3 pathway and Beclin-1-LC3-p62 pathway, thereby regulates both apoptosis and autophagy. Finally, we showed that AB4-induced apoptosis and autophagy converges at the PI3K/Akt/mTOR signaling. AB4 treatment inhibits this signaling transduction pathway and leads to HCC cell death. Collectively, our study highlighted the anti-cancer efficacy of AB4 and suggested that AB4 might be a novel way to treat HCC.</p>
</div>
</front>
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<name sortKey="Liu, Guoxin" sort="Liu, Guoxin" uniqKey="Liu G" first="Guoxin" last="Liu">Guoxin Liu</name>
<name sortKey="Liu, Xu" sort="Liu, Xu" uniqKey="Liu X" first="Xu" last="Liu">Xu Liu</name>
<name sortKey="Liu, Yang" sort="Liu, Yang" uniqKey="Liu Y" first="Yang" last="Liu">Yang Liu</name>
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<name sortKey="Zhou, Yu" sort="Zhou, Yu" uniqKey="Zhou Y" first="Yu" last="Zhou">Yu Zhou</name>
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