Background: Tumor hypoxia induces the expression of growth arrest and DNA damage-inducible protein (GADD34). However, the role of GADD34 in tumor growth remains unclear.
Materials and methods: Gadd34 expression was knocked-down through lentivirus-mediated short hairpin RNA (shRNA) in tumor cells, which were subsequently injected subcutaneously into mice. Tumor volumes and myeloid-derived suppressor cells (MDSCs) were monitored. Isolated MDSCs were incubated with tumor supernatant to investigate the impact of GADD34 on cytokine secretion of MDSCs.
Results: We observed that reduction of GADD34 expression significantly suppressed tumor, and resulted in decreased accumulation of MDSCs and T-cells, and inhibition of GADD34 reduced secretion of vascular epithelial growth factor α and transforming growth factor β by MDSCs.
Conclusion: These findings provide a promising strategy for targeting GADD34 activity in order to inhibit tumor growth.
Keywords: GADD34; Gr1+CD11b+ MDSC; Lewis lung carcinoma; TGFβ; VEGFA.
Copyright© 2016 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved.