Oncocalyxone A from Auxemma oncocalyx lacks genotoxic activity in phytohemagglutinin-stimulated lymphocytes.

C Pessoa, F M A C Vieira, T G Lemos, M O Moraes, P D L Lima, S H B Rabenhorst, A Leyva, R R Burbano
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引用次数: 7

Abstract

Inadequate doses or prolonged chemotherapy can be cytotoxic or genotoxic to cancer patients, increasing the risk for the development of a second cancer, particularly acute leukemia. The association between therapeutic and genotoxic properties of oncocalyxone A (Onco A), make cytotoxic tests (mitotic index and chromosomal aberrations) fundamental in the accompaniment of the effects of this active compound. Therefore, the aim of the present study was to determine the genotoxic action of Onco A in vitro, during different phases of the cell cycle, utilizing primary cultures of lymphocytes of healthy individuals. The results showed that Onco A is cytotoxic during the cell cycle phases G1, G1/S, and S, however, not in G2. Onco A did not demonstrate a genotoxic effect in any of the cell cycle phases at the concentration studied. It is concluded that during the period of exposure, this active substance inhibits DNA synthesis and consequently cell division. Therefore, the absence of such genotoxicity for Onco A in the tests performed in this study provides important information in regard to the therapeutic use of this agent. Further studies are necessary to better understand the molecular mechanism of action of Onco A.

来自Auxemma oncocalyone A在植物血凝素刺激淋巴细胞中缺乏基因毒性活性。
剂量不足或化疗时间过长会对癌症患者产生细胞毒性或基因毒性,增加患第二种癌症的风险,尤其是急性白血病。肿瘤calyxone A (Onco A)的治疗和基因毒性特性之间的关联,使得细胞毒性测试(有丝分裂指数和染色体畸变)在这种活性化合物的作用下是基本的。因此,本研究的目的是利用健康个体淋巴细胞的原代培养物,确定Onco A在细胞周期不同阶段的体外遗传毒性作用。结果表明,Onco A在细胞周期G1、G1/S和S期具有细胞毒性,而在G2期不具有细胞毒性。在研究的浓度下,Onco A在任何细胞周期阶段都没有表现出遗传毒性作用。由此得出结论,在暴露期间,这种活性物质抑制DNA合成,从而抑制细胞分裂。因此,在本研究中进行的试验中,Onco A没有这种遗传毒性,这为该药物的治疗用途提供了重要信息。为了更好地了解Onco A的分子作用机制,还需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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