Related Experiment Video
Updated: May 5, 2026

Establishment of Hepatocarcinoma in BALB/c-nu Mice and Investigation of the Therapeutic Effect of the Sanleng Jiashen Formula
Published on: January 26, 2024
Effect of Celergen, a marine derivative, on in vitro hepatocarcinogenesis
R Catanzaro1, N Zerbinati, U Solimene
1ReGenera Research Group for Aging-Intervention, Milano, Italy.
Abstract:
The aim of this study was to test for a potential anticarcinogenic effect of Celergen, a marine derivative devoid of traceable amounts of inorganic arsenic, on cell proliferation, cell cycle progression and apoptosis in the HepG2 human liver cancer cell line. Celergen significantly inhibited the proliferation of cancer cells in a dose-dependent manner while limiting the cell cycle progression at the G1 phase and significantly inducing apoptosis. Further examination showed that Celergen enhanced expression of the p21(CIPl1WAF1), GADD153 genes and downregulated the c-myc gene. These results suggest that Celergen exerts promising chemopreventive properties to be further investigated.
Insights
Celergen, a marine derivative, shows potential as a liver cancer chemopreventive. It inhibited HepG2 cancer cell proliferation, induced apoptosis, and altered key gene expressions, warranting further investigation.
Area of Science:
- Marine Biology
- Cancer Research
- Molecular Biology
Background:
- Hepatocellular carcinoma (HCC) remains a significant global health challenge.
- Developing novel chemopreventive agents is crucial for cancer management.
- Celergen, a marine-derived compound, is being investigated for its therapeutic potential.
Purpose of the Study:
- To evaluate the anticarcinogenic effects of Celergen on the HepG2 human liver cancer cell line.
- To assess Celergen's impact on cancer cell proliferation, cell cycle, and apoptosis.
- To explore the molecular mechanisms underlying Celergen's potential chemopreventive properties.
Main Methods:
- HepG2 cells were treated with varying concentrations of Celergen.
- Cell proliferation was assessed using standard assays.
- Cell cycle progression and apoptosis were analyzed via flow cytometry.
- Gene expression levels of p21(CIPl1WAF1), GADD153, and c-myc were quantified.
Main Results:
- Celergen significantly inhibited HepG2 cell proliferation in a dose-dependent manner.
- Celergen treatment led to cell cycle arrest at the G1 phase.
- Significant induction of apoptosis was observed in Celergen-treated cells.
- Celergen upregulated p21(CIPl1WAF1) and GADD153 gene expression while downregulating c-myc.
Conclusions:
- Celergen demonstrates promising chemopreventive properties against liver cancer.
- The compound effectively inhibits cancer cell proliferation and induces apoptosis.
- Molecular changes in p21, GADD153, and c-myc suggest a role in Celergen's mechanism of action.
- Further research is warranted to explore Celergen's therapeutic potential in vivo.
More Related Videos
Related Concept Videos
Mutagenicity and Carcinogenicity
Liver Regeneration
Cells of Liver
The liver comprises four major types of cells— hepatocytes, stellate, Kupffer, and sinusoidal endothelial cells. The hepatocytes are...
In vitro Mutagenesis
In-vitro Mutagenesis

