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PLoS One. 2013 Dec 12;8(12):e83195. doi: 10.1371/journal.pone.0083195. eCollection 2013.

Pegylated interferon-α2a inhibits proliferation of human liver cancer cells in vitro and in vivo.

Author information

1
Department of Pathology, Kurume University School of Medicine, Kurume, Fukuoka, Japan.
2
Department of Clinical Laboratory Medicine, Kurume University Hospital, Kurume, Fukuoka, Japan.

Abstract

PURPOSE:

We investigated the effects of pegylated interferon-α2a (PEG-IFN-α2a) on the growth of human liver cancer cells.

METHODS:

The effect of PEG-IFN-α2a on the proliferation of 13 liver cancer cell lines was investigated in vitro. Cells were cultured with medium containing 0-4,194 ng/mL of PEG-IFN-α2a, and after 1, 2, 3, or 4 days of culture, morphologic observation and growth assay were performed. After hepatocellular carcinoma (HCC) cells (HAK-1B and KIM-1) were transplanted into nude mice, various doses of PEG-IFN-α2a were subcutaneously administered to the mice once a week for 2 weeks, and tumor volume, weight, and histology were examined.

RESULTS:

PEG-IFN-α2a inhibited the growth of 8 and 11 cell lines in a time- and dose-dependent manner, respectively, although the 50% growth inhibitory concentrations of 7 measurable cell lines on Day 4 were relatively high and ranged from 253 ng/mL to 4,431 ng/mL. Various levels of apoptosis induction were confirmed in 8 cell lines. PEG-IFN-α2a induced a dose-dependent decrease in tumor volume and weight, and a significant increase of apoptotic cells in the tumor. Subcutaneous administration of clinical dose for chronic hepatitis C (3 μg/kg, 0.06 μg/mouse) was effective and induced about 30-50% reduction in the tumor volume and weight as compared with the control.

CONCLUSIONS:

Although in vitro anti-proliferative effects of PEG-IFN-α2a were relatively weak, PEG-IFN-α2a induced strong anti-tumor effects on HCC cells in vivo. The data suggest potential clinical application of PEG-IFN-α2a for the prevention and treatment of HCC.

PMID:
24349459
PMCID:
PMC3861497
DOI:
10.1371/journal.pone.0083195
[Indexed for MEDLINE]
Free PMC Article
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