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脱氧胞苷对人T淋巴细胞白血病细胞中胸苷毒性的挽救机制

Mechanism of deoxycytidine rescue of thymidine toxicity in human T-leukemic lymphocytes.

作者信息

Fox R M, Tripp E H, Tattersall M H

出版信息

Cancer Res. 1980 May;40(5):1718-21.

PMID:6989492
Abstract

Cultured malignant human lymphocytes are highly sensitive to growth inhibition by thymidine (50% inhibitory dose congruent to 10(-5) M). Growth inhibition reflects sustained elevation of the deoxythymidine 5'-triphosphate pool associated with secondary elevation of the deoxyguanosine 5'-triphosphate pool and reduction in the deoxycytidine 5'-triphosphate (dCTP) pool. Deoxycytidine was capable of partially reversing thymidine growth inhibition at a concentration of 0.5 microM, and growth recovery was virtually complete at 8 microM. The dCTP pool remained depressed until growth inhibition reversal by deoxycytidine was complete, and at a higher concentration of deoxycytidine the dCTP rose above control levels, but the deoxythymidine 5'-triphosphate and deoxyguanosine 5'-triphosphate pools remained elevated. These results support the view that thymidine growth inhibition induces a critical deficiency of dCTP via allosteric inhibition of ribonucleotide reductase rather than inhibiting DNA replication directly by elevated deoxythymidine 5'-triphosphate or deoxyguanosine 5'-triphosphate pools.

摘要

培养的恶性人淋巴细胞对胸苷的生长抑制高度敏感(50%抑制剂量相当于10^(-5) M)。生长抑制反映了脱氧胸苷5'-三磷酸池的持续升高,这与脱氧鸟苷5'-三磷酸池的继发性升高以及脱氧胞苷5'-三磷酸(dCTP)池的减少有关。脱氧胞苷在浓度为0.5 microM时能够部分逆转胸苷的生长抑制,在8 microM时生长恢复几乎完全。dCTP池一直处于压低状态,直到脱氧胞苷完全逆转生长抑制,并且在更高浓度的脱氧胞苷下,dCTP上升至对照水平之上,但脱氧胸苷5'-三磷酸和脱氧鸟苷5'-三磷酸池仍保持升高。这些结果支持这样一种观点,即胸苷生长抑制通过核糖核苷酸还原酶的变构抑制诱导dCTP的关键缺乏,而不是通过升高的脱氧胸苷5'-三磷酸或脱氧鸟苷5'-三磷酸池直接抑制DNA复制。

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