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化疗在非人类灵长类动物中诱导的染色体畸变程度取决于给药方案。

The extent of chromosomal aberrations induced by chemotherapy in non-human primates depends on the schedule of administration.

作者信息

Rao V Koneti, Knutsen Turid, Ried Thomas, Wangsa Darawalee, Flynn Bernard Mike, Langham Gregory, Egorin Merrill J, Cole Diane, Balis Frank, Steinberg Seth M, Bates Susan, Fojo Tito

机构信息

Center for Cancer Research, National Cancer Institute, NIH, Building 10, Rm 12N226, 9000 Rockville Pike, Bethesda, MD 20892, USA.

出版信息

Mutat Res. 2005 Jun 6;583(2):105-19. doi: 10.1016/j.mrgentox.2005.01.013.

Abstract

We utilized a non-human primate model, the rhesus monkey (Macaca mulatta), to quantitate the extent of chromosomal damage in bone marrow cells following chemotherapy. Thiotepa, etoposide, and paclitaxel were chosen as the chemotherapy agents due to their distinct mechanisms of action. Chromosomal aberrations were quantitated using traditional Giemsa stain. We sought to evaluate the extent to which genotoxicity was dependent on the schedule of administration by giving chemotherapy as either a bolus or a 96 h continuous infusion. Neutropenia and areas under the concentration curve (AUCs) were monitored to ensure comparable cytotoxicity and dose administered. At least 100 metaphases were scored in each marrow sample by an investigator unaware of the treatment history of the animals. All three drugs produced a statistically significant higher percentage of abnormal metaphases following bolus chemotherapy (p<0.0001, p=0.0015 and p<0.0001 for thiotepa, etoposide and paclitaxel, respectively). We conclude that infusional administration of thiotepa, etoposide and paclitaxel is less genotoxic to normal bone marrow cells than is bolus administration. These results suggest infusional regimens may be considered where there are concerns about long-term genotoxic sequelae, including secondary cancer, teratogenicity, or possibly the development of drug resistance. We believe this approach provides a reproducible model in which drugs and eventually, regimens can be compared.

摘要

我们利用一种非人类灵长类动物模型——恒河猴(猕猴),来定量化疗后骨髓细胞中的染色体损伤程度。由于噻替派、依托泊苷和紫杉醇的作用机制不同,故而选择它们作为化疗药物。使用传统吉姆萨染色法对染色体畸变进行定量。我们试图通过给予一次性推注或96小时持续输注化疗药物,来评估基因毒性在多大程度上取决于给药方案。监测中性粒细胞减少症和浓度曲线下面积(AUC),以确保细胞毒性和给药剂量具有可比性。由一名对动物治疗史不知情的研究人员对每个骨髓样本中至少100个中期相进行评分。三种药物在一次性推注化疗后产生的异常中期相百分比均具有统计学意义上的显著升高(噻替派、依托泊苷和紫杉醇分别为p<0.0001、p = 0.0015和p<0.0001)。我们得出结论,与一次性推注给药相比,噻替派、依托泊苷和紫杉醇的输注给药对正常骨髓细胞的基因毒性较小。这些结果表明,在担心长期基因毒性后遗症(包括继发性癌症、致畸性或可能出现的耐药性)的情况下,可以考虑采用输注方案。我们认为这种方法提供了一个可重复的模型,在这个模型中可以比较药物,最终比较给药方案。

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