Analysis of some metabolic conditions promoting selective sensitivity of tumor cells to peroxidative stress.

P M Schwartzburd, K B Aslanidi
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Abstract

Some metabolic parameters enhancing the sensitivity of tumor cells and their lipoprotein refractive granules (RG) to peroxidative stress were investigated during the growth cycle of ascite tumors in vivo. The majority of tumor cells only in the stationary growth phase had the increased sensitivity to peroxidative stress, tested by fluorescence intensivity of peroxidation products. The increase of this intensity correlates well with the decrease of tumor proliferation, the functional activity of mitochondria, the cellular level of ATP and extracellular pH. These metabolic conditions are favourable for increasing the neutral lipid accumulation in the stationary tumor cells, their RG and nuclei, as compared to exponentially growing cells. The sensitivity of tumor cells to peroxidation can be also enhanced with the help of exogenous polyunsaturated fatty acid (PUFA). Based on literature and our own data on Ehrlich ascites carcinoma (EAC), a working hypothesis is proposed to explain the enhanced selective sensitivity of tumor cells to PUFA peroxidation products (PP) suppressing the cell growth (especially in the stationary phase of EAC growth).

促进肿瘤细胞对过氧化应激选择性敏感性的一些代谢条件的分析。
在体内研究了腹水肿瘤生长周期中增强肿瘤细胞及其脂蛋白折射颗粒(RG)对过氧化应激敏感性的代谢参数。通过过氧化产物的荧光强度检测,大多数肿瘤细胞仅在稳定生长期对过氧化应激的敏感性增加。这种强度的增加与肿瘤增殖、线粒体功能活性、细胞ATP水平和细胞外ph的降低密切相关。与呈指数增长的细胞相比,这些代谢条件有利于增加静止肿瘤细胞、RG和细胞核中的中性脂质积累。外源性多不饱和脂肪酸(PUFA)也可以增强肿瘤细胞对过氧化的敏感性。基于文献和我们自己对Ehrlich腹水癌(EAC)的数据,我们提出了一个有效的假设来解释肿瘤细胞对PUFA过氧化产物(PP)的选择性敏感性增强,抑制了细胞的生长(特别是在EAC生长的固定阶段)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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