Metabolic Effects of 3′-Deoxyadenosine (Cordycepin) and 2-Halo-3′-Deoxyadenosine on Repair of X-Ray-Induced Potentially Lethal Damage in Chinese Hamster V79 Cells
Wakako Hiraoka, Kiyoshi Tanabe, Mikinori Kuwabara, Fumiaki Sato
Abstract
Wakako Hiraoka, Kiyoshi Tanabe, Mikinori Kuwabara, Fumiaki Sato
Abstract
Using cultured Chinese hamster V79 cells, an attempt has been made to examine the phosphorylation of cordycepin and its 2-halo derivatives (2-chloro-3'-deoxyadenosine, 2-bromo-3'-deoxyadenosine, and 2-iodo-3'-deoxyadenosine) by adenosine kinase, within the cells, and to correlate it with their cytotoxicities and abilities to inhibit the repair of X-ray-induced potentially lethal damage (PLDR). Of all compounds, only cordycepin was found to be phosphorylated and showed both potent cytotoxicity and ability to inhibit PLDR.
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Using cultured Chinese hamster V79 cells, an attempt has been made to examine the phosphorylation of cordycepin and its 2-halo derivatives (2-chloro-3'-deoxyadenosine, 2-bromo-3'-deoxyadenosine, and 2-iodo-3'-deoxyadenosine) by adenosine kinase, within the cells, and to correlate it with their cytotoxicities and abilities to inhibit the repair of X-ray-induced potentially lethal damage (PLDR). Of all compounds, only cordycepin was found to be phosphorylated and showed both potent cytotoxicity and ability to inhibit PLDR.
Key concepts: Cordycepin, Deoxyadenosine, Chinese hamster, Adenosine, Cytotoxicity, Adenosine kinase, Biochemistry, DNA damage