Claudia Campani, Manuela Capone, Francesco Liotta, Umberto Arena, Valentina Adotti, Chiara Di Bonaventura, Sami Aburas, Stefano Colagrande, Linda Calistri, Francesco Annunziato, Fabio Marra
Journal: Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2022;54(7):911-917
PMID: 34876355
BACKGROUND AND AIMS
Circulating endothelial progenitor cells (EPC) predict tumor vascularization and disease progression, but limited information is available on their dynamics in hepatocellular carcinoma (HCC) undergoing systemic treatment.
METHODS
We prospectively analyzed different populations of EPC in 16 patients with advanced HCC receiving sorafenib. Patients were studied before therapy (T0, n = 16) and after two (T2, n = 12) and eight weeks (T8, n = 8), using high-performance flow-cytometry. The tumor response at T8 was categorized as progressive disease (PD) or clinical benefit (CB, all other responses).
RESULTS
At T0, higher levels of CD34CD133KDR and CD34KDR were observed in patients with alpha-fetoprotein ≥400 ng/ml or non-viral liver disease, whereas CD34CD133KDR cells were virtually absent in patients with vascular invasion. CD34KDR and CD34CD133KDR were directly correlated with platelet count. Frequencies of all populations of EPC declined in patients receiving sorafenib. Levels of CD34CD133 were higher at T0 in patients with CB compared to patients with PD. In patients belonging to the CB group CD34KDR cells at T0 were directly correlated to platelet count.
CONCLUSION
In patients with advanced HCC, EPC are directly correlated with platelet count, suggesting a common activation of selected bone marrow pathways. Levels of a CD34KDR are higher at baseline in patients responding to sorafenib.
Copyright © 2021. Published by Elsevier Ltd.
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