Purpose: Human papillomavirus (HPV)-16 oncoproteins, E6 and E7, are associated with enhanced tumor angiogenesis in human cervical cancers. The purpose of this study was (a) to investigate whether expression of HPV-16 E6 and E7 oncoproteins induces hypoxia-inducible factor 1a (HIF-1a) and vascular endothelial growth factor expression in cervical cancer cells; and (b) to assess the effect of resveratrol on 16 E6-and E7-induced HIF-1a and VEGF gene expression. Experimental Design: Human cervical cancer cell lines C-33A and HeLa were transiently cotransfected with pSG5-HPV-16 E6 or 16 E7 constructs along with HIF-1a small interfering RNA (siRNA) or nonspecific siRNA. The expression of HIF-1a/VEGF was measured using realtime PCR, Western blot analysis, or ELISA. The in vitro angiogenic activity induced by 16 E6-and E7-transfected cells was examined. The effect of resveratrol on oncoprotein-induced HIF-1a/VEGF expression and in vitro angiogenesis was investigated. Results: HPV-16 E6-and E7-transfected cervical cancer cells express increased HIF-1a protein andVEGF expression.These stimulatory effects were abrogated by cotransfection with either HIF1a siRNA or treatment with resveratrol. Blocking extracellular signal-regulated kinase 1/2 (ERK 1/ 2) and phosphoinositide-3-kinase by PD98059 and LY294002, respectively, abolished 16 E6-and E7-induced HIF-1aand VEGF expression. Functionally, we showed that HPV-16 E6-and E7-transfected cervical cancer cells stimulated in vitro capillary or tubule formation, and these angiogenic effects could be abolished either by cotransfection with HIF-1asiRNA or by treatment with resveratrol. Conclusion: HPV-16 oncoproteins contribute to enhanced angiogenesis in cervical cancer cells via HIF-1a^dependentVEGF expression. Resveratrol suppresses 16 E6-and E7-induced HIF-1am ediated angiogenic activity and, thus, is a promising chemotherapeutic agent for human cervical cancer.