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两种靶向拓扑异构酶(II)的蒽环类药物的染色体畸变和微核研究

Chromosomal aberration and micronucleus studies of two topoisomerase (II) targeting anthracyclines.

作者信息

Khan Fauzia, Sherwani Asma Farhat, Afzal Mohammad

机构信息

Department of Zoology, Aligarh Muslim University, Aligarh, India.

出版信息

J Environ Biol. 2009 May;30(3):409-12.

Abstract

Anthracycline antibiotics are widely used in cancer chemotherapy. Doxorubicin and Idarubicin, topoisomerase-targeting anthracyclines, were examined for their effect on chromosomal aberration and micronucleus induction in cultured human lymphocytes employing lymphocyte transformation test and cytokinesis-blocked micronucleus (CBMN) assay. A statistically significant dose-dependent increase in micronucleus frequency (p < 0.001) in binucleated cells was seen as well as a significant increase in chromosomal aberration frequency was also observed for both the drugs. A variety of aberrations were scored including terminal deletions, breaks, gaps, exchanges, fragment formation, ends rejoining, interstitial deletions etc. Nuclear division index was also calculated and showed a cell cycle delay towards higher doses. A number of necrotic and apoptotic cells were also observed at higher concentrations. This confirms the two drugs to be clastogenic and aneugenic.

摘要

蒽环类抗生素广泛应用于癌症化疗。采用淋巴细胞转化试验和胞质分裂阻滞微核(CBMN)试验,研究了拓扑异构酶靶向蒽环类药物阿霉素和伊达比星对培养的人淋巴细胞染色体畸变和微核诱导的影响。观察到双核细胞中微核频率有统计学意义的剂量依赖性增加(p < 0.001),并且两种药物的染色体畸变频率也有显著增加。对包括末端缺失、断裂、间隙、交换、片段形成、末端重连、中间缺失等多种畸变进行了评分。还计算了核分裂指数,结果显示在较高剂量下细胞周期延迟。在较高浓度下还观察到许多坏死和凋亡细胞。这证实这两种药物具有致断裂和致染色体非整倍体的作用。

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