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阿糖胞苷、博来霉素和培普利霉素对艾氏腹水瘤细胞体内长期治疗的细胞生长抑制和细胞毒性反应。

Cytostatic and cytotoxic response of Ehrlich ascites tumor cells in vivo on chronic treatment with cytarabine, bleomycin, and peplomycin.

作者信息

Stoehr M, Friedel G, Engel P, Goerttler K, Futterman G

出版信息

Arzneimittelforschung. 1984;34(4):451-4.

PMID:6204650
Abstract

The cytokinetic response of Ehrlich ascites tumor (EAT) cells in vivo upon chronic treatment at low dosage levels with cytarabine (1-beta-D-arabinofuranosylcytosine, ara-c) bleomycin (BLM) and peplomycin (PEP) was estimated. Bivariate DNA histograms allow the simultaneous evaluation of the cell cycle status of living and killed cells. It could be confirmed that ara-C is cytostatic on cells in S phase. Pronounced cytotoxicity was observed in G1 and G2+M phase. BLM and PEP showed no (or neglectable ) accumulation of vital cells in any cycle phase. Both drugs, however, are cytotoxic on cells, regardless their position within the cell cycle. A successive application of ara-C and BLM (or PEP) in a cell kinetics-directed therapy schedule may be taken into account.

摘要

评估了用阿糖胞苷(1-β-D-阿拉伯呋喃糖基胞嘧啶,ara-c)、博来霉素(BLM)和培普利霉素(PEP)在低剂量水平对艾氏腹水瘤(EAT)细胞进行长期体内治疗后的细胞动力学反应。双变量DNA直方图可同时评估活细胞和死细胞的细胞周期状态。可以确认,阿糖胞苷对S期细胞具有细胞生长抑制作用。在G1期和G2+M期观察到明显的细胞毒性。BLM和PEP在任何细胞周期阶段均未显示(或可忽略不计)活细胞的积累。然而,这两种药物对细胞均具有细胞毒性,无论其在细胞周期中的位置如何。可以考虑在细胞动力学导向的治疗方案中连续应用阿糖胞苷和BLM(或PEP)。

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