Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2866119 | The American Journal of Pathology | 2007 | 13 Pages |
In this study, we examined the possible involvement of progenitor cells in the carcinogenesis of human hepatocellular carcinoma (HCC) using tissue specimens and cell lines. We used ATP-binding cassette transporter ABCG2 as a progenitor cell marker. Immunohistochemically, ABCG2+ hepatocytes were observed in the periportal areas of the dysplastic nodule, and ABCG2+ cancer cells were also scattered or focally clustered in HCC. We sorted the cultured HCC cells (HuH7 and PLC5) into ABCG2+ and ABCG2− subpopulations and then subcultured them for 4 weeks. ABCG2+ cells could generate ABCG2+ and ABCG2− progenies during subculture, whereas ABCG2− cells bore only ABCG2− cells, suggesting that a cancer cell hierarchy with reference to ABCG2 exists in HCC cells and that ABCG2+ cells reside at the higher rank in that hierarchy. Interestingly, other progenitor cell markers including cytokeratin 19 and α-fetoprotein were mainly expressed in ABCG2+ subpopulations. Conversely, albumin expression was more intense in ABCG2− cells. In addition, the expression patterns of transcription factors (GATA6, CCAAT/enhancer-binding protein α, and CCAAT/enhancer-binding protein β) in ABCG2+ and ABCG2− cells resembled those during normal liver development. In conclusion, this study suggests that cancer cells with ABCG2 expression might play a central role in hepatocarcinogenesis and the maintenance of the cancer cell hierarchy of human HCC.