Abstract
Hypoxia inducible factor 1α (HIF-1α) is highly expressed and is implicated in the progression of esophageal squamous cell carcinoma. To investigate the potential mechanism by which HIF-1α contributes to the progression of esophageal squamous cell carcinoma, here we established stable esophageal carcinoma cell lines Eca-109 and TE-13 in which HIF-1α was depleted by shRNA mediated gene silencing. In addition, we used specific inhibitor YC-1 to inhibit HIF-1α expression. Our in vitro studies demonstrated that shRNA or chemical mediated inhibition of HIF-1α led to reduced proliferation and increased apoptosis of esophageal carcinoma cells, as well as the downregulatuion of HIF-1α targets VEGF, MMP2 and BCL2. Furthermore, we employed xenograft nude mice model to validate the in vitro findings and proved that depletion of HIF-1α suppressed the tumorigenicity of esophageal carcinoma cells in vivo. In conclusion, our results provide new insight into the potential role of HIF-1α in esophageal squamous cell carcinoma and open up the possibility of inhibiting HIF-1α for targeted therapy of esophageal squamous cell carcinoma. © 2011 Landes Bioscience.
Author supplied keywords
Cite
CITATION STYLE
Zhu, H., Feng, Y., Zhang, J., Zhou, X., Hao, B., Zhang, G., & Shi, R. (2011). Inhibition of hypoxia inducible factor 1α expression suppresses the progression of esophageal squamous cell carcinoma. Cancer Biology and Therapy, 11(11), 981–987. https://doi.org/10.4161/cbt.11.11.15707
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.