Abstract
Axitinib, a selective inhibitor of vascular endothelial growth factor receptor (VEGFR), is used as an anti-angiogenic agent for the treatment of metastatic renal cell carcinoma (RCC). However, the effect of axitinib on antitumor immunity has remained largely unexplored. In this study, we show that while axitinib (25mg/kg) significantly suppresses tumor growth and metastasis, thus prolonging life span in murine RCC xenografts, the treatment leads to a major decrease in the number of myeloid-derived suppressor cells (MDSCs) in the spleens and tumor beds of animals, which in turn promotes antitumor responses of CD8+ T-cells in vivo. Moreover, as one of the main transcription factors that regulate MDSC function, Signal transducer and activator of transcription 3 (STAT3) was also significantly inhibited in the Renca tumor-associated MDSC and tumor tissues. These results suggest that axitinib has the potential to modulate antitumor immunity by downregulating STAT3 expression and reversing MDSC-mediated tumor-induced immunosuppression. The study reveals the unique antitumor mechanism of axitinib and provided useful information for its clinical application.
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