Grune T, Siems W G, Zollner H, Esterbauer H
Clinics of Physical Therapy and Rehabilitation, Medical Faculty (Charité), Humboldt University, Berlin, Germany.
Cancer Res. 1994 Oct 1;54(19):5231-5.
The aldehydic lipid peroxidation product 4-hydroxynonenal (HNE) is cytotoxic at high concentrations (in the range of 100 microM); at low concentrations, it disturbs cell proliferation and exhibits genotoxic effects, and in the submicromolar range, HNE is chemotactic and stimulates phospholipase C. HNE is rapidly metabolized in eukaryotic cells. Here the metabolism of HNE was studied in suspensions of Ehrlich mouse ascites cells at different periods of the tumor age. The main products of HNE which were identified in the Ehrlich ascites cells, were glutathione-HNE-conjugate, hydroxynonenoic acid, and 1,4-dihydroxynonene. The formation of glutathione conjugates following the addition of HNE was higher in early phase cells when compared with cells in the late phase of tumor growth. That was in accordance with the increased consumption of the reduced form of glutathione. Ehrlich ascites tumor cells at the proliferation phase were able to reduce a higher amount of exogenous-added HNE, compared with cells at the stationary phase.
醛类脂质过氧化产物4-羟基壬烯醛(HNE)在高浓度(100微摩尔范围内)具有细胞毒性;在低浓度时,它会干扰细胞增殖并表现出遗传毒性,而在亚微摩尔范围内,HNE具有趋化作用并刺激磷脂酶C。HNE在真核细胞中会迅速代谢。在此,研究了不同肿瘤年龄阶段的艾氏小鼠腹水细胞悬液中HNE的代谢情况。在艾氏腹水细胞中鉴定出的HNE主要产物为谷胱甘肽-HNE缀合物、羟基壬烯酸和1,4-二羟基壬烯。与肿瘤生长后期的细胞相比,在早期细胞中加入HNE后谷胱甘肽缀合物的形成更高。这与还原型谷胱甘肽消耗的增加相一致。与静止期的细胞相比,增殖期的艾氏腹水肿瘤细胞能够还原更多外源性添加的HNE。