Ochi T, Cerutti P A
Proc Natl Acad Sci U S A. 1987 Feb;84(4):990-4. doi: 10.1073/pnas.84.4.990.
Phorbol 12-myristate 13-acetate induces the release of a low molecular weight clastogenic factor from monocytes. Hydroperoxy-5,8,11,13-icosatetraenoic acids represent major components of clastogenic factor. We report that several isomeric hydroperoxy-5,8,11,13-icosatetraenoic acids efficiently induce DNA strand breakage and/or alkali-labile sites in the mouse embryo fibroblasts C3H/10T1/2. Fe chelation by desferrioxamine suppresses breakage by approximately equal to 42% indicating the participation of Fe-catalyzed radical reactions. An additional 37% inhibition is observed upon addition of the Ca2+ chelators EGTA and quin-2. This result suggests that hydroxyperoxy-5,8,11,13-icosatetraenoic acid may activate a Ca2+-dependent nuclease. The addition of the antioxidant enzymes CuZn-superoxide dismutase and catalase had no effect, while glutathione peroxidase suppressed strand breakage by 90%. To our knowledge, our results yield a first insight into the mechanism of action of monocyte clastogenic factor and the role of inflammation in tumor promotion.
佛波醇12 -肉豆蔻酸酯13 -乙酸酯可诱导单核细胞释放一种低分子量的致断裂因子。氢过氧-5,8,11,13-二十碳四烯酸是致断裂因子的主要成分。我们报告称,几种异构的氢过氧-5,8,11,13-二十碳四烯酸能有效诱导小鼠胚胎成纤维细胞C3H/10T1/2中的DNA链断裂和/或碱不稳定位点。去铁胺的铁螯合作用可使断裂减少约42%,表明铁催化的自由基反应参与其中。加入Ca2+螯合剂EGTA和喹啉-2后,又观察到37%的抑制作用。这一结果表明,氢过氧-5,8,11,13-二十碳四烯酸可能激活一种Ca2+依赖性核酸酶。添加抗氧化酶铜锌超氧化物歧化酶和过氧化氢酶没有效果,而谷胱甘肽过氧化物酶可使链断裂减少90%。据我们所知,我们的结果首次深入了解了单核细胞致断裂因子的作用机制以及炎症在肿瘤促进中的作用。