Neuzil J, Weber T, Terman A, Weber C, Brunk U T
Institute for Prevention of Cardiovascular Diseases, Ludwig Maximilians University, Munich, Germany.
Redox Rep. 2001;6(3):143-51. doi: 10.1179/135100001101536247.
Recent evidence suggests that vitamin E and its analogues, which have been used for many years as antioxidants, may not only protect cells from free radical damage but also induce apoptotic cell death in various cell types. While alpha-tocopherol (alpha-TOH) is mainly known as an anti-apoptotic agent, its redox-silent analogues either have no influence on cell survival (alpha-tocopheryl acetate, alpha-TOA), or induce apoptosis (alpha-tocopheryl succinate, alpha-TOS). Although precise mechanisms of apoptosis induction by alpha-TOS remain to be elucidated, there is evidence that this process involves both the antiproliferative and membrane destabilising activities of the agent. Alpha-TOS has been shown to induce apoptosis in malignant cell lines but not, in general, in normal cells, and to inhibit tumorigenesis in vivo. These features suggest that this semi-synthetic analogue of vitamin E could be a promising antineoplastic agent.
最近的证据表明,多年来一直用作抗氧化剂的维生素E及其类似物,不仅可以保护细胞免受自由基损伤,还能在多种细胞类型中诱导凋亡性细胞死亡。虽然α-生育酚(α-TOH)主要被认为是一种抗凋亡剂,但其氧化还原沉默类似物要么对细胞存活没有影响(α-生育酚乙酸酯,α-TOA),要么诱导凋亡(α-生育酚琥珀酸酯,α-TOS)。尽管α-TOS诱导凋亡的确切机制仍有待阐明,但有证据表明该过程涉及该试剂的抗增殖和膜不稳定活性。α-TOS已被证明能在恶性细胞系中诱导凋亡,但一般不在正常细胞中诱导凋亡,并且能在体内抑制肿瘤发生。这些特性表明,这种维生素E的半合成类似物可能是一种有前景的抗肿瘤药物。