E2EPF Ubiquitin Carrier Protein-Von Hippel-Lindau Interaction and Uses Thereof
The present invention relates to the E2 EPF UCP-VHL interaction and the uses thereof, more precisely a method for increasing or reducing VHL activity or level by regulating UCP activity or level to inhibit cancer cell proliferation or metastasis or to increase angiogenesis. The inhibition of UCP activity is accomplished by any UCP activity inhibitor selected from a group consisting of a small interfering RNA (RNAi), an antisense oligonucleotide, and a polynucleotide complementarily binding to mRNA of UCP, a peptide, a peptide mimetics and an antibody, and a low molecular compound. In the meantime, the increase of angiogenesis is accomplished by the following mechanism; UCP over-expression is induced by a gene carrier and thus endogenous VHL is reduced, leading to the stabilization of HIF-1α which enhances VEGF activation based on the HIF-1α stabilization. The method for regulating UCP activity or level results in the increase or decrease of VHL activity or level, so that it can be applied to the development of an anticancer agent and an angiogenesis inducer.
1 - 57 . (canceled)
58 . A method for stimulating angiogenesis in a subject, including the step of administering a pharmaceutically effective dosage of a Ubiquitin Carrier Protein (UCP) activity enhancer, an expression vector with the insertion of UCP gene or a UCP protein to the subject.
59 . The method according to claim 58 , wherein the UCP activity enhancer reduces Von Hippel-Lindau (VHL) activity or level.
60 . The method according to claim 58 , wherein the UCP activity enhancer increases Hypoxia-inducible factor (HIF) stability.
61 . The method according to claim 58 , wherein the UCP activity enhancer increases expression of angiogenesis factors such as vascular epithelial growth factor (VEGF).
62 . The method according to claim 58 , wherein the UCP activity enhancer mediates by a UCP mRNA expression inducer stimulating UCP promoter and a plasmid or a virus gene carrier inducing UCP expression.
63 . A method for treating ischemic diseases, including the step of administering a pharmaceutically effective dosage of a Ubiquitin carrier protein (UCP) activity enhancer, an expression vector with the insertion of UCP gene or a UCP protein to the subject.
64 . The method of claim 63 , wherein the UCP activity enhancer is a UCP mRNA expression inducer stimulating UCP promoter, a plasmid or a virus gene carrier inducing UCP expression.
65 . The method according to claim 63 , wherein the UCP activity enhancer reduces Von Hippel-Lindau (VHL) activity or level.
66 . The method according to claim 63 , wherein the UCP activity enhancer increases Hypoxia-inducible factor (HIF) stability.
67 . The method according to claim 63 , wherein the UCP activity enhancer increases expression of angiogenesis factors such as vascular epithelial growth factor (VEGF).
68 . The method according to claim 63 , wherein the UCP activity enhancer mediates by a UCP mRNA expression inducer stimulating UCP promoter and a plasmid or a virus gene carrier inducing UCP expression.