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Antitumor activity of a sulfated polysaccharide from Enteromorpha intestinalis targeted against hepatoma through mitochondrial pathway
- Source :
- Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine. 35(2)
- Publication Year :
- 2013
-
Abstract
- A sulfated polysaccharide (EI-SP), extracted from Enteromorpha intestinalis that is a kind of algae, is found to have anticancer activity. This study was designed to investigate the anti-tumor effect of EI-SP on human hepatoma HepG2 cell line and its possible mechanisms. An MTT assay showed that EI-SP could specifically inhibit the growth of human hepatoma HepG2 cells in a dose-dependent manner. Analysis by flow cytometry indicated that the apoptosis of tumor cells increased after treatment with EI-SP in range of 100–400 μg/ml. Furthermore, Western blot analysis showed that EI-SP treatment led to decreased protein expression of Bcl-2 and an increase in Bax, cleaved caspase-3, cleaved caspase-9 and cleaved poly(ADP-ribose) polymerase (PARP). Moreover, it was found that EI-SP caused a loss of mitochondrial membrane potential (Δψ m) and the release of cytochrome c to the cytosol. Collectively, our results showed that the EI-SP induces apoptosis in HepG2 cells involving a caspases-mediated mitochondrial signalling pathway.
- Subjects :
- Carcinoma, Hepatocellular
Poly ADP ribose polymerase
Apoptosis
Flow cytometry
Ulva
Western blot
Polysaccharides
medicine
Humans
MTT assay
Polymerase
Cell Proliferation
bcl-2-Associated X Protein
biology
medicine.diagnostic_test
Cytochrome c
Liver Neoplasms
General Medicine
Hep G2 Cells
Flow Cytometry
Molecular biology
Mitochondria
Gene Expression Regulation, Neoplastic
Cytosol
Biochemistry
Proto-Oncogene Proteins c-bcl-2
Caspases
biology.protein
Signal Transduction
Subjects
Details
- ISSN :
- 14230380
- Volume :
- 35
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine
- Accession number :
- edsair.doi.dedup.....a7af926bc03ce3cc40da3066d6131c49