Androgen Receptor Enhances the Efficacy of Sorafenib Against Hepatocellular Carcinoma Through Enriched EpCAM Stemness
| Autor: | Chun Mien Chang, Wei Chun Chang, Pei Yin Liao, Yu Ting Su, Wen Lung Ma, Long Bin Jeng, Wei Min Chung, Chun Chieh Yeh, Hsueh Chou Lai |
|---|---|
| Rok vydání: | 2020 |
| Předmět: |
Sorafenib
Male Cancer Research Carcinoma Hepatocellular Transfection 03 medical and health sciences Transactivation Mice 0302 clinical medicine Cell Line Tumor medicine Animals Humans Protein kinase A neoplasms Protein kinase B Cell growth Chemistry Kinase Liver Neoplasms General Medicine medicine.disease Epithelial Cell Adhesion Molecule digestive system diseases Androgen receptor Oncology Receptors Androgen 030220 oncology & carcinogenesis Hepatocellular carcinoma Cancer research medicine.drug |
| Zdroj: | Anticancer research. 40(3) |
| ISSN: | 1791-7530 |
| Popis: | Background/aim The role of androgen receptor (AR) in hepatocellular carcinoma (HCC) development is controversial. Therefore, the translational value of targeting AR in HCC is unknown. Sorafenib, a multiple kinase inhibitor, is the standard therapy for patients with unresectable HCC. This study investigated sorafenib effect on AR in experimental models of HCC. Material and methods AR cDNA was introduced into HCC cells and in vitro cell growth and in vivo tumor growth were measured. Sphere cells, as well as epithelial cell adhesion molecule-positive (EpCAM+) and CD133+ cells were isolated from HCC cells with/without AR expression to observe in vitro/in vivo effects. Liver specific AR knockout in mouse models of spontaneous HCC (carcinogen-induced and hepatitis B virus-related HCC) was also implemented to examine gene expression. HCC cells/tumors were treated with sorafenib in order to determine effects on tumor growth and related gene expression. Result AR cDNA increased transactivation function, increased colony/sphere-forming activities, and enhanced tumorigenicity in HCC cells compared to their parental cells. Expression of the stemness marker EpCAM was also dramatically increased. In carcinogen-and HBV-induced HCC models, EpCAM+ cells were significantly reduced in AR-knockout mice compared to wild-type HCCs. In addition, AR reduced sorafenib-related signals, e.g. extracellular-regulated kinase, AKT serine/threonine kinase 1, and p38 mitogen-activated protein kinase, compared to that in parental cells. Regarding sorafenib cytotoxicity, AR-expressing cells were vulnerable to treatment. Moreover, the half maximal-inhibitory concentration (IC50) was drastically lowered in AR+/EpCAM+ compared to AR-/EpCAM- sphere cells. Strikingly, the IC50 in AR+/CD133+ vs. AR-/CD133+ cells were similar. Moreover, sorafenib robustly suppressed tumor growth in implanted AR+/EpCAM+ cells but not AR-/EpCAM- ones. Finally, bioinformatics analyses revealed EpCAM to be a prognostic biomarker in Asian and non-alcohol-consuming patients with HCC, suggesting suitability of a sorafenib regimen for such patients. Conclusion AR+/EpCAM+ may be a marker of responsiveness to sorafenib for patients with HCC. Prospective surveys associating AR/EpCAM expression with therapy outcomes are essential. |
| Databáze: | OpenAIRE |
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