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Novel Small Molecular Compound AE-848 Showed Potent Inhibitory Activity Against Human Hepatoblastoma Cells
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Abstract
Purpose
AE-848/33345007, is a novel small molecular compound that was independently synthesized by our laboratory. The aim of the current study was to investigate potential therapeutic effects of the small molecule compound AE-848 on human hepatoblastoma cells.
Methods
Human hepatoblastoma cell line HepG2 was cultured under different concentrations of AE-848. MTT assay was used to detect the inhibitory ability of AE-848 on the activity of this cell line, while flow cytometry was applied to quantify apoptosis. Western-blot technique was used to determine expression levels of signaling pathway-associated molecules. The antitumor
in vivo
activity of AE-848 against hepatoblastoma was evaluated using hepatoblastoma-bearing nude mice randomly divided into AE-848 (experimental) and saline (control) groups respectively. Changes in survival and tumor sizes were compared between these two groups.
Results
AE-848 significantly inhibited proliferation and induced apoptosis of HepG2 cells, and induced activation of PI3K/Akt/mTOR signaling pathways. More importantly, AE-848 administration significantly inhibited tumor growth and prolonged survival of hepatoblastoma-bearing mice.
Conclusion
AE-848 had a strong anti-hepatoblastoma activity both
in vitro
and
in vivo
, indicating the importance of developing AE-848 as a potential drug for hepatoblastoma treatment.
Title: Novel Small Molecular Compound AE-848 Showed Potent Inhibitory Activity Against Human Hepatoblastoma Cells
Description:
Abstract
Purpose
AE-848/33345007, is a novel small molecular compound that was independently synthesized by our laboratory.
The aim of the current study was to investigate potential therapeutic effects of the small molecule compound AE-848 on human hepatoblastoma cells.
Methods
Human hepatoblastoma cell line HepG2 was cultured under different concentrations of AE-848.
MTT assay was used to detect the inhibitory ability of AE-848 on the activity of this cell line, while flow cytometry was applied to quantify apoptosis.
Western-blot technique was used to determine expression levels of signaling pathway-associated molecules.
The antitumor
in vivo
activity of AE-848 against hepatoblastoma was evaluated using hepatoblastoma-bearing nude mice randomly divided into AE-848 (experimental) and saline (control) groups respectively.
Changes in survival and tumor sizes were compared between these two groups.
Results
AE-848 significantly inhibited proliferation and induced apoptosis of HepG2 cells, and induced activation of PI3K/Akt/mTOR signaling pathways.
More importantly, AE-848 administration significantly inhibited tumor growth and prolonged survival of hepatoblastoma-bearing mice.
Conclusion
AE-848 had a strong anti-hepatoblastoma activity both
in vitro
and
in vivo
, indicating the importance of developing AE-848 as a potential drug for hepatoblastoma treatment.
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