Thomas T, Thomas T J
Department of Environmental and Community Medicine, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, New Brunswick 08903, USA.
Cell Mol Life Sci. 2001 Feb;58(2):244-58. doi: 10.1007/PL00000852.
Polyamines are aliphatic cations with multiple functions and are essential for life. Cellular polyamine levels are regulated by multiple pathways such as synthesis from amino acid precursors, cellular uptake mechanisms that salvage polyamines from diet and intestinal microorganisms, as well as stepwise degradation and efflux. Investigations using polyamine biosynthetic inhibitors indicate that alterations in cellular polyamine levels modulate normal and cancer cell growth. Studies using transgenic mice overexpressing polyamine biosynthetic enzymes support a role of polyamines in carcinogenesis. Many, if not all, signal transduction pathways intersect with polyamine biosynthetic pathways and the regulation of intracellular polyamine levels. Direct binding of polyamines to DNA and their ability to modulate DNA-protein interactions appear to be important in the molecular mechanisms of polyamine action in cell proliferation. Consistent with the role of polyamines as facilitators of cell growth, several studies have shown their ability to protect cells from apoptosis. However, polyamines also have a role in facilitating cell death. The basis of these diverse cellular responses is currently not known. Cell death response might be partly mediated by the production of hydrogen peroxide during polyamine catabolism. In addition, the ability of polyamines to alter DNA-protein and protein-protein interactions might be disruptive to cellular functions, when abnormally high levels are accumulated due to defects in polyamine catabolic or efflux pathways. A large body of data indicates that polyamine pathway can be a molecular target for therapeutic intervention in several types cancers. Inhibitors of biosynthesis, polyamine analogues as well as oligonucleotide/polyamine analogue combinations are promising drug candidates for chemoprevention and/or treatment of cancer.
多胺是具有多种功能的脂肪族阳离子,对生命至关重要。细胞内多胺水平受多种途径调控,如由氨基酸前体合成、从饮食和肠道微生物中回收多胺的细胞摄取机制,以及逐步降解和外排。使用多胺生物合成抑制剂的研究表明,细胞内多胺水平的改变可调节正常细胞和癌细胞的生长。使用过表达多胺生物合成酶的转基因小鼠进行的研究支持了多胺在致癌过程中的作用。许多(如果不是全部)信号转导途径与多胺生物合成途径以及细胞内多胺水平的调节相互交叉。多胺与DNA的直接结合及其调节DNA - 蛋白质相互作用的能力,在细胞增殖过程中多胺作用的分子机制中似乎很重要。与多胺作为细胞生长促进剂的作用一致,多项研究表明它们具有保护细胞免于凋亡的能力。然而,多胺在促进细胞死亡方面也有作用。目前尚不清楚这些不同细胞反应的基础。细胞死亡反应可能部分由多胺分解代谢过程中过氧化氢的产生介导。此外,当由于多胺分解代谢或外排途径缺陷而积累异常高水平的多胺时,多胺改变DNA - 蛋白质和蛋白质 - 蛋白质相互作用的能力可能会破坏细胞功能。大量数据表明,多胺途径可能是几种癌症治疗干预的分子靶点。生物合成抑制剂、多胺类似物以及寡核苷酸/多胺类似物组合是化学预防和/或癌症治疗的有前景的候选药物。