核糖核苷酸还原酶和胸苷激酶活性的各种培养细胞系源自血液恶性肿瘤。

Gan Pub Date : 1984-09-01
E Takeda, M Hirose, Y Kuroda, T Ninomiya, K Toshima, T Watanabe, M Ito, E Naito, M Miyao
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引用次数: 0

摘要

测定了16株培养的不同增殖率的人血液恶性细胞株的核糖核苷酸还原酶和胸苷激酶活性以及胸苷掺入率。胸苷激酶活性在髓系和单核细胞系中明显高于其他细胞系,而核糖核苷酸还原酶活性在不同细胞系中表现为CDP还原酶活性相似。胸苷激酶与CDP还原酶活性的比值在单核细胞中较高。细胞增殖率与CDP还原酶活性密切相关,与胸腺嘧啶激酶活性和胸腺嘧啶掺入率无关。慢生长细胞系胸苷激酶与CDP还原酶活性之比高,快生长细胞系胸苷激酶与CDP还原酶活性之比低。这些结果表明,在培养的人恶性细胞中,高增殖潜力可能主要依赖于DNA生物合成的从头合成嘧啶途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ribonucleotide reductase and thymidine kinase activities in various cultured cell lines derived from hematologic malignancies.

The activities of ribonucleotide reductase and thymidine kinase, and the thymidine incorporation rate were measured in 16 cultured human hematologic malignant cell lines with different cell proliferation rates. Thymidine kinase activity was significantly higher in myeloid and monocytoid cell lines than in other cell lines, but ribonucleotide reductase activity presented as CDP reductase activity was similar in the different cell lines. The ratio of thymidine kinase to CDP reductase activity was high in monocytoid cell lines. A close correlation was found between the cell proliferation rate and CDP reductase activity, but not thymidine kinase activity or the thymidine incorporation rate. The ratio of thymidine kinase to CDP reductase activity was high in slowly growing cell lines and low in rapidly growing cell lines. These results indicate that in cultured human malignant cells a high potential for proliferation may depend mainly on the de novo pyrimidine pathway of DNA biosynthesis.

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Gan
Gan
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