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钠钾ATP酶α亚基作为抗癌治疗的新靶点。

Na+/K+-ATPase alpha subunits as new targets in anticancer therapy.

作者信息

Mijatovic Tatjana, Ingrassia Laurent, Facchini Vincenzo, Kiss Robert

机构信息

Unibioscreen SA, Brussels, Belgium.

出版信息

Expert Opin Ther Targets. 2008 Nov;12(11):1403-17. doi: 10.1517/14728222.12.11.1403.

Abstract

BACKGROUND

The sodium pump (Na(+)/K(+)-ATPase) could be a target for the development of anticancer drugs as it serves as a signal transducer, it is a player in cell adhesion and its aberrant expression and activity are implicated in the development and progression of different cancers. Cardiotonic steroids (CS) are the natural ligands and inhibitors of the sodium pump and this supports the possibility of their development as anticancer agents targeting overexpressed Na(+)/K(+)-ATPase alpha subunits.

OBJECTIVES

To highlight and further develop the concept of using Na(+)/K(+)-ATPase alpha1 and alpha3 subunits as targets in anticancer therapy and to address the question of the actual usefulness of further developing CS as anticancer agents.

CONCLUSIONS

Targeting overexpressed Na(+)/K(+)-ATPase alpha subunits using novel CS might open a new era in anticancer therapy and bring the concept of personalized medicine from aspiration to reality. Clinical data are now needed to further support this proposal. Furthermore, future medicinal chemistry should optimize new anticancer CS to target Na(+)/K(+)-ATPase alpha subunits with the aim of rendering them more potent and less toxic.

摘要

背景

钠泵(Na⁺/K⁺-ATP酶)可作为抗癌药物开发的靶点,因为它充当信号转导器,参与细胞黏附,其异常表达和活性与不同癌症的发生和发展有关。强心甾类化合物(CS)是钠泵的天然配体和抑制剂,这支持了将其开发为靶向过表达的Na⁺/K⁺-ATP酶α亚基的抗癌药物的可能性。

目的

强调并进一步发展将Na⁺/K⁺-ATP酶α1和α3亚基作为抗癌治疗靶点的概念,并探讨进一步开发CS作为抗癌药物的实际效用问题。

结论

使用新型CS靶向过表达的Na⁺/K⁺-ATP酶α亚基可能会开启抗癌治疗的新纪元,并使个性化医疗的概念从愿望变为现实。现在需要临床数据来进一步支持这一建议。此外,未来的药物化学应优化新型抗癌CS,以靶向Na⁺/K⁺-ATP酶α亚基,使其更有效且毒性更小。

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