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砷对有丝分裂进程的破坏

Disruption of Mitotic Progression by Arsenic.

作者信息

States J Christopher

机构信息

Department of Pharmacology and Toxicology, University of Louisville, 505 S. Hancock St, Louisville, KY, 40202, USA,

出版信息

Biol Trace Elem Res. 2015 Jul;166(1):34-40. doi: 10.1007/s12011-015-0306-7. Epub 2015 Mar 22.

Abstract

Arsenic is an enigmatic xenobiotic that causes a multitude of chronic diseases including cancer and also is a therapeutic with promise in cancer treatment. Arsenic causes mitotic delay and induces aneuploidy in diploid human cells. In contrast, arsenic causes mitotic arrest followed by an apoptotic death in a multitude of virally transformed cells and cancer cells. We have explored the hypothesis that these differential effects of arsenic exposure are related by arsenic disruption of mitosis and are differentiated by the target cell's ability to regulate or modify cell cycle checkpoints. Functional p53/CDKN1A axis has been shown to mitigate the mitotic block and to be essential to induction of aneuploidy. More recent preliminary data suggest that microRNA modulation of chromatid cohesion also may play a role in escape from mitotic block and in generation of chromosomal instability. Other recent studies suggest that arsenic may be useful in treatment of solid tumors when used in combination with other cytotoxic agents such as cisplatin.

摘要

砷是一种神秘的外源性物质,它会引发包括癌症在内的多种慢性疾病,同时也是一种在癌症治疗中颇具前景的治疗药物。砷会导致二倍体人类细胞出现有丝分裂延迟并诱导非整倍体产生。相比之下,砷会使多种病毒转化细胞和癌细胞发生有丝分裂停滞,随后引发凋亡性死亡。我们探讨了这样一种假说,即砷暴露的这些不同效应与砷对有丝分裂的破坏有关,并且通过靶细胞调节或修改细胞周期检查点的能力来区分。功能性p53/CDKN1A轴已被证明可减轻有丝分裂阻滞,并且对于诱导非整倍体至关重要。最近的初步数据表明,微小RNA对染色单体凝聚的调节也可能在摆脱有丝分裂阻滞和产生染色体不稳定性方面发挥作用。其他近期研究表明,砷与顺铂等其他细胞毒性药物联合使用时,可能对实体瘤治疗有用。

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