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多胺在决定细胞对化疗药物的反应中的作用:蛋白激酶 CK2 表达和活性的调节。

Role of polyamines in determining the cellular response to chemotherapeutic agents: modulation of protein kinase CK2 expression and activity.

机构信息

Department of Biochemistry and Molecular Biology, University of Southern Denmark, Campusvej 55, 5230 Odense, Denmark.

出版信息

Mol Cell Biochem. 2011 Oct;356(1-2):149-58. doi: 10.1007/s11010-011-0949-4. Epub 2011 Jul 13.

Abstract

Numerous studies have shown that platinum compounds stimulate the expression of the polyamine catabolic enzyme spermidine/spermine N(1)-acetyltransferase resulting in anti-proliferative activity and apoptosis. As many cancer cell types including pancreatic cancer cells express high levels of polyamines, the possibility to develop anti-tumor strategies to deplete polyamine pools has drawn considerable attention in recent years. This has been effectively accomplished by treating cells with platinum drugs in combination with polyamine analogs such as N(1),N(11)-diethylnorspermine (DENSPM). The present study, examined the cytotoxic effects of oxaliplatin in combination with stimulators of polyamine catabolism in human pancreatic cancer cells, that are notoriously resistant to chemotherapeutic treatment, and colorectal cancer cells. Additionally, as protein kinase CK2 has been shown to be an anti-apoptotic and pro-survival enzyme regulated by the intracellular polyamine pools, we aimed to investigate the effect of combined DENSPM and oxaliplatin treatment on CK2-mRNA and -protein levels. Results reported here show that treatment with oxaliplatin and DENSPM in combination impairs cell viability particularly in the case of colorectal cancer cells. The analysis of CK2 expression and activity indicates that the response to a specific treatment may depend on the impact that individual compounds exert on pro-survival and pro-death proteins at the transcription and translation levels that should be carefully evaluated in view of subsequent clinical studies.

摘要

许多研究表明,铂化合物刺激多胺分解酶精脒/精胺 N(1)-乙酰基转移酶的表达,从而具有抗增殖活性和细胞凋亡作用。由于许多癌细胞类型包括胰腺癌细胞表达高水平的多胺,因此近年来开发耗尽多胺池的抗肿瘤策略引起了相当大的关注。通过用铂药物联合多胺类似物如 N(1),N(11)-二乙基-norspermine(DENSPM)治疗细胞,可以有效地实现这一点。本研究检查了奥沙利铂与多胺分解代谢刺激物联合在人胰腺癌细胞中的细胞毒性作用,这些细胞对化疗治疗具有明显的抗性,以及结直肠癌细胞。此外,由于蛋白激酶 CK2 已被证明是一种抗凋亡和生存促进酶,受细胞内多胺池调节,我们旨在研究联合 DENSPM 和奥沙利铂治疗对 CK2-mRNA 和 -蛋白水平的影响。这里报告的结果表明,奥沙利铂和 DENSPM 的联合治疗特别会损害结肠直肠癌细胞的细胞活力。对 CK2 表达和活性的分析表明,对特定治疗的反应可能取决于单个化合物在转录和翻译水平上对生存和死亡促进蛋白的影响,应根据随后的临床研究仔细评估。

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