Przybyszewski Waldemar M, Kasperczyk Janusz
Zakład Radiobiologii Doświadczalnej i Klinicznej, Centrum Onkologii--Instytut im. M. Skłodowskiej-Curie, Oddział w Gliwicach.
Postepy Hig Med Dosw (Online). 2006;60:516-26.
It has been shown that hydroxyurea (HU) induces free radicals which exert cytotoxic effects on cells. However, the molecular mechanism of this effect is still obscure. A possible mechanism for HU-mediated cell death induced by unbalanced growth could be the overproduction, altered accumulation, and progressive leakage of many hydrolytic enzymes through the cell membrane, leading to "lytic" cell death. Protection by antioxidants and radicals scavengers does not change the inhibition of DNA synthesis dependent on ribonucleotide reductase, the main mechanism of the antineoplastic activity of HU. These observations support the hypothesis that membranes are targets for the side effects of HU toxicity. Damage of erythrocytes and granulocytes seems to be an important clinical feature of the HU side toxicity generating free radicals.
已经表明,羟基脲(HU)会诱导自由基,这些自由基对细胞产生细胞毒性作用。然而,这种作用的分子机制仍然不清楚。由生长失衡介导的HU诱导细胞死亡的一种可能机制可能是许多水解酶的过量产生、积累改变以及通过细胞膜的渐进性渗漏,导致“溶解性”细胞死亡。抗氧化剂和自由基清除剂的保护作用不会改变依赖于核糖核苷酸还原酶的DNA合成抑制,这是HU抗肿瘤活性的主要机制。这些观察结果支持了细胞膜是HU毒性副作用靶点的假说。红细胞和粒细胞的损伤似乎是HU产生自由基的副作用的一个重要临床特征。