Avila Matías A, García-Trevijano Elena R, Lu Shelly C, Corrales Fernando J, Mato José M
Division of Hepatology and Gene Therapy, F.I.M.A, University of Navarra, Pamplona, Spain.
Int J Biochem Cell Biol. 2004 Nov;36(11):2125-30. doi: 10.1016/j.biocel.2003.11.016.
5'-Methylthioadenosine (MTA) is a naturally occurring sulfur-containing nucleoside present in all mammalian tissues. MTA is produced from S-adenosylmethionine mainly through the polyamine biosynthetic pathway, where it behaves as a powerful inhibitory product. This compound is metabolized solely by MTA-phosphorylase, to yield 5-methylthioribose-1-phosphate and adenine, a crucial step in the methionine and purine salvage pathways, respectively. Abundant evidence has accumulated over time suggesting that MTA can affect cellular processes in many ways. MTA has been shown to influence numerous critical responses of the cell including regulation of gene expression, proliferation, differentiation and apoptosis. Although most of these responses have been observed at the pharmacological level, their specificity makes it tempting to speculate that endogenous MTA could play a regulatory role in the cell. Finally, observations carried out in models of liver damage and cancer demonstrate a therapeutic potential for MTA that deserves further consideration.
5'-甲硫腺苷(MTA)是一种天然存在的含硫核苷,存在于所有哺乳动物组织中。MTA主要通过多胺生物合成途径由S-腺苷甲硫氨酸产生,在该途径中它作为一种强效抑制产物发挥作用。这种化合物仅由MTA磷酸化酶代谢,生成5-甲硫基核糖-1-磷酸和腺嘌呤,分别是甲硫氨酸和嘌呤补救途径中的关键步骤。随着时间的推移,大量证据不断积累,表明MTA可以通过多种方式影响细胞过程。已证明MTA会影响细胞的许多关键反应,包括基因表达调控、增殖、分化和凋亡。尽管这些反应大多是在药理学水平上观察到的,但它们的特异性让人不禁推测内源性MTA可能在细胞中发挥调节作用。最后,在肝损伤和癌症模型中进行的观察表明MTA具有治疗潜力,值得进一步研究。