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米托蒽醌联合热疗对人慢性髓性白血病细胞的体外作用

Effect of mitoxantrone on human chronic myeloid leukemia cells in vitro, combined with hyperthermia.

作者信息

Juvekar A S, Chitnis M P, Adwankar M K, Advani S H

出版信息

Neoplasma. 1986;33(4):477-82.

PMID:3463880
Abstract

Mitoxantrone, a new anticancer drug has DNA-binding properties similar to anthracycline antibiotics. In the present studies, effect of the drug has been tested in vitro on human chronic myeloid leukemia cells at 37 degrees C and 42 degrees C. Inhibition of 3H-tritiated thymidine incorporation in the drug-treated cells compared with untreated cells has been used as the parameter of cytotoxicity of the drug and hyperthermia. Cell samples from 11 CML patients who did not receive any chemotherapy showed less response to the drug at 0.5 micrograms/ml and 1 microgram/ml at 37 degrees C. Exposure of CML cells to 42 degrees C for 2 h indicated 13 to 44% inhibition in 3H-TdR incorporation. However, when CML cells were exposed to mitoxantrone for 2 h at 42 degrees C the 3H-thymidine incorporation was inhibited to the extent of 27 to 71%, indicating greater cellular damage with this combination.

摘要

米托蒽醌是一种新型抗癌药物,具有与蒽环类抗生素相似的DNA结合特性。在本研究中,已在体外对人慢性粒细胞白血病细胞于37℃和42℃下测试了该药物的作用。与未处理细胞相比,药物处理细胞中3H-氚标记胸腺嘧啶核苷掺入的抑制作用已被用作该药物和热疗细胞毒性的参数。来自11名未接受任何化疗的慢性粒细胞白血病患者的细胞样本在37℃下对0.5微克/毫升和1微克/毫升的药物反应较小。将慢性粒细胞白血病细胞暴露于42℃ 2小时表明3H-TdR掺入受到13%至44%的抑制。然而,当慢性粒细胞白血病细胞在42℃下暴露于米托蒽醌2小时时,3H-胸腺嘧啶核苷掺入被抑制至27%至71%的程度,表明这种联合作用对细胞的损伤更大。

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