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下一代基于钒的药物诱导的细胞阻滞和细胞凋亡:作用机制与结构关系及未来展望。

Cell Arrest and Apoptosis Induced by the Next Generation of Vanadium Based Drugs: Action Mechanism to Structure Relation and Future Perspectives.

机构信息

Department of Life and Health Sciences, Pharmacy Programme University of Nicosia, 46 Makedonitissas Avenue, CY- 2417, P.O. Box 24005, CY-1700, Nicosia, Cyprus.

出版信息

Anticancer Agents Med Chem. 2021 Oct 28;21(16):2111-2116. doi: 10.2174/1871520621666201222143839.

Abstract

BACKGROUND

Every year, we encounter more projects indicating the promising anticancer activity of vanadium molecules against different types of cancer cells. The new generation of metal-based drugs, targets the energy supplies of the cell through ROS generation leading them to cell arrest and apoptosis. The relatively low toxicity of vanadium metal, the different oxidation states that it can occur and in general, the lipophilicity of transition metals, gave attention to vanadium after the exhausting research in platinum-based drugs. Herein, the latest advances in the apoptotic activity of vanadium complex molecules have been reviewed and revealed the structure to action relationship. Future perspectives of vanadium anticancer drugs are also discussed.

METHODS

Data were collected from Web of Science, Scopus, Pubmed, through searching of these keywords: "apoptosis", "anticancer drugs", "vanadium complexes", "synthesis" and "cell arrest".

RESULTS

A good amount of vanadium complexes gave promising results over the past few years, showing that a more careful approach of a ligand design could give rise to the next generation of vanadium drugs.

CONCLUSION

The low toxicity of vanadium ion in combination with its V(IV) species selectivity gives the vanadium a head starts against other transition metal complexes.

摘要

背景

每年,我们都会遇到更多的项目,表明钒分子对不同类型的癌细胞具有有前景的抗癌活性。新一代基于金属的药物通过生成 ROS 来靶向细胞的能量供应,从而导致细胞停滞和凋亡。钒金属的毒性相对较低,它可以存在的不同氧化态,以及过渡金属的普遍亲脂性,使得人们在对铂类药物进行了大量研究之后,开始关注钒。本文综述了钒配合物分子在细胞凋亡活性方面的最新进展,并揭示了结构与活性的关系。还讨论了钒类抗癌药物的未来展望。

方法

通过在 Web of Science、Scopus、Pubmed 上搜索以下关键词:“凋亡”、“抗癌药物”、“钒配合物”、“合成”和“细胞停滞”,从这些数据库中收集数据。

结果

在过去的几年中,大量的钒配合物取得了有希望的结果,这表明更仔细的配体设计方法可能会产生下一代的钒药物。

结论

钒离子的低毒性与其 V(IV)物种选择性相结合,使钒在对抗其他过渡金属配合物方面具有优势。

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