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紫杉醇、辐射与致癌转化

Taxol, radiation, and oncogenic transformation.

作者信息

Hei T K, Hall E J

机构信息

Center for Radiological Research, College of Physicians & Surgeons, Columbia University, New York, New York 10032.

出版信息

Cancer Res. 1993 Mar 15;53(6):1368-72.

PMID:8095180
Abstract

The novel antineoplastic drug taxol has been shown to be active clinically against several types of human tumors. With improvement in treatment strategy and the number of long-term survivors increasing, a question that needs to be addressed is the potential carcinogenic effect of the treatment in the induction of second malignancies. We show here that when tested using an in vitro assay for oncogenic transforming potential, taxol is ineffective in focus induction at doses significantly higher than those used in the clinic. However, taxol enhances the oncogenic potential of gamma-rays in a synergistic fashion. The fact that taxol blocks cells at the G2/M phases of the cell cycle may account for this interaction since G2/M are relatively radiosensitive phases of the cell cycle.

摘要

新型抗肿瘤药物紫杉醇已在临床上显示出对多种人类肿瘤具有活性。随着治疗策略的改进以及长期存活者数量的增加,一个需要解决的问题是该治疗在诱发第二原发恶性肿瘤方面的潜在致癌作用。我们在此表明,当使用体外致癌转化潜能测定法进行测试时,紫杉醇在剂量显著高于临床使用剂量时,对焦点诱导无效。然而,紫杉醇以协同方式增强了γ射线的致癌潜能。紫杉醇使细胞阻滞在细胞周期的G2/M期这一事实可能解释了这种相互作用,因为G2/M期是细胞周期中相对放射敏感的阶段。

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