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Protection against DNA damage-induced apoptosis by the angiogenic factor thymidine phosphorylase
Authors:Jeung Hei-Cheul  Che Xiao-Fang  Haraguchi Misako  Zhao Hong-Ye  Furukawa Tatsuhiko  Gotanda Takenari  Zheng Chun-Lei  Tsuneyoshi Kengo  Sumizawa Tomoyuki  Roh Jae Kyung  Akiyama Shin-Ichi
Affiliation:Department of Molecular Oncology, Graduate School of Medical and Dental Sciences, Kagoshima University, 8-35-1, Sakuragaoka, Kagoshima 890-8520, Japan.
Abstract:Thymidine phosphorylase (TP) is involved both in pyrimidine nucleoside metabolism and in angiogenesis. TP also conferred the resistance to hypoxia-induced apoptosis of the cancer cells. In U937 cells, DNA damage-inducing agents significantly enhanced the expression of TP. Cell lines stably transfected with TP cDNA were more resistant to the DNA damage-inducing agents than the mock-transfected cells and showed augmented activity of Akt. The cytoprotective function of TP against DNA damage was independent of its enzymatic activity. The resistance to apoptosis was partially abrogated by treatment with the phosphatidyl inositol 3-kinase (PI3K) inhibitors, suggesting that the cytoprotective function of TP is mediated, at least in part, by regulation of the PI3K/Akt pathway. These findings indicate that TP expression in increased by various stress including DNA damage and that TP molecules confer resistance to DNA damage-induced apoptosis in cancer cells.
Keywords:Thymidine phosphorylase   Apoptosis   Akt
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