Peters J, Baron D, Kiefer G, Glaesener J J, Hug J, Hagedorn M
Arch Dermatol Res (1975). 1976 Dec 15;257(2):185-94. doi: 10.1007/BF00558092.
The incorporation of 14C-marked nucleotides and amino acids into the nucleic acids and into the cellular protein of PHA-stimulated human lymphocytes was inhibited variably by increasing doses of Adriamycin, Bleomycin and Na2HAsO4. The findings, which were obtained with the aid of the liquid scintillation counter and partly by means of 14C-thymidine-marked autoradiographies shows clearly that Adriamycin causes the strongest incorporation inhibition. In contrast to this, the inhibition caused by Bleomycin and arsenate is considerably less destructive. It was shown by means of cytophoto metrical examinations that Adriamycin is capable of fixing cells in the G2 phase and in the S phase. Cells react similarly to Bleomycin and arsenate. The differential inhibition of nucleic acid and protein metabolism induced by Adriamycin, Bleomycin and arsenate is correlated with a varying responsiveness of lymphocytes to the cytostatically effective substances.
用递增剂量的阿霉素、博来霉素和砷酸氢二钠(Na2HAsO4)处理后,14C标记的核苷酸和氨基酸掺入PHA刺激的人淋巴细胞的核酸及细胞蛋白中的过程受到不同程度的抑制。借助液体闪烁计数器并部分通过14C-胸腺嘧啶标记的放射自显影术获得的结果清楚地表明,阿霉素引起的掺入抑制作用最强。与此相反,博来霉素和砷酸盐引起的抑制作用破坏性要小得多。通过细胞光度学检查表明,阿霉素能够使细胞停滞在G2期和S期。细胞对博来霉素和砷酸盐的反应相似。阿霉素、博来霉素和砷酸盐对核酸和蛋白质代谢的差异抑制与淋巴细胞对这些具有细胞抑制作用的物质的不同反应性相关。