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多胺与癌症:对化疗和化学预防的影响。

Polyamines and cancer: implications for chemotherapy and chemoprevention.

机构信息

Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD 21287, USA.

出版信息

Expert Rev Mol Med. 2013 Feb 22;15:e3. doi: 10.1017/erm.2013.3.

Abstract

Polyamines are small organic cations that are essential for normal cell growth and development in eukaryotes. Under normal physiological conditions, intracellular polyamine concentrations are tightly regulated through a dynamic network of biosynthetic and catabolic enzymes, and a poorly characterised transport system. This precise regulation ensures that the intracellular concentration of polyamines is maintained within strictly controlled limits. It has frequently been observed that the metabolism of, and the requirement for, polyamines in tumours is frequently dysregulated. Elevated levels of polyamines have been associated with breast, colon, lung, prostate and skin cancers, and altered levels of rate-limiting enzymes in both biosynthesis and catabolism have been observed. Based on these observations and the absolute requirement for polyamines in tumour growth, the polyamine pathway is a rational target for chemoprevention and chemotherapeutics. Here we describe the recent advances made in the polyamine field and focus on the roles of polyamines and polyamine metabolism in neoplasia through a discussion of the current animal models for the polyamine pathway, chemotherapeutic strategies that target the polyamine pathway, chemotherapeutic clinical trials for polyamine pathway-specific drugs and ongoing clinical trials targeting polyamine biosynthesis.

摘要

多胺是真核生物中正常细胞生长和发育所必需的小有机阳离子。在正常生理条件下,细胞内多胺浓度通过生物合成和分解代谢酶的动态网络以及一个特征尚不明确的运输系统进行严格调节。这种精确的调节确保了细胞内多胺浓度维持在严格控制的范围内。人们经常观察到,肿瘤中多胺的代谢和需求经常失调。多胺水平升高与乳腺癌、结肠癌、肺癌、前列腺癌和皮肤癌有关,并且观察到生物合成和分解代谢中限速酶的水平发生改变。基于这些观察结果以及肿瘤生长对多胺的绝对需求,多胺途径是化学预防和化疗的合理靶点。在这里,我们描述了多胺领域的最新进展,并通过讨论多胺途径的当前动物模型、针对多胺途径的化疗策略、多胺途径特异性药物的化疗临床试验以及针对多胺生物合成的正在进行的临床试验,重点讨论了多胺和多胺代谢在肿瘤发生中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b6e/4027058/dc0fb804c0a8/nihms-458055-f0001.jpg

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