Laboratorio de Radioisótopos, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Argentina.
Toxicol Lett. 2012 Sep 3;213(2):184-93. doi: 10.1016/j.toxlet.2012.06.017. Epub 2012 Jul 4.
It has reported that many environmental compounds may display estrogenic actions and these findings led to researchers to associate breast cancer risk with the use of some pesticides. The aim of this work was to investigate the effect of chlorpyrifos (CPF) on cell proliferation and the ERα-dependence of this action employing MCF-7 and MDA-MB-231 breast cancer cell lines. We have also analyzed CPF action on the cell cycle distribution and the cyclins that are implicated in G1-S and intra-S checkpoints. Finally, the action on cell death and ROS production were studied. We demonstrated the ability of CPF 0.05μM to induce cell proliferation through ERα in hormone-dependent breast cancer cells. In contrast, CPF 50μM induces intra-S arrest modifying checkpoints proteins, through a mechanism that may involve changes in redox balance in MCF-7. In MDA-MB-231, we have found that CPF 50μM produces an arrest in G2/M phase which could be related to the capacity of the pesticide for binding to tubulin sites altering microtubules polymerization. Altogether, our results provide new evidences on the action of the pesticide CPF as an environmental breast cancer risk factor due to the effects that causes on the mechanisms that modulate breast cell proliferation.
据报道,许多环境化合物可能表现出雌激素作用,这些发现导致研究人员将乳腺癌风险与使用某些农药联系起来。本工作的目的是研究氯吡硫磷 (CPF) 对 MCF-7 和 MDA-MB-231 乳腺癌细胞系细胞增殖的影响及其对 ERα 的依赖性。我们还分析了 CPF 对细胞周期分布的作用,以及与 G1-S 和内 S 检查点相关的细胞周期蛋白。最后,研究了细胞死亡和 ROS 产生的作用。我们证明了 0.05μM CPF 通过 ERα 诱导激素依赖性乳腺癌细胞增殖的能力。相比之下,50μM CPF 通过一种可能涉及氧化还原平衡变化的机制诱导内 S 期阻滞,改变 MCF-7 中的检查点蛋白。在 MDA-MB-231 中,我们发现 50μM CPF 导致 G2/M 期阻滞,这可能与该农药与微管蛋白结合位点结合改变微管聚合的能力有关。总之,我们的结果为 CPF 作为环境乳腺癌风险因素的作用提供了新的证据,因为它对调节乳腺细胞增殖的机制产生了影响。