Cohen Marie, Pierredon Sandra, Wuillemin Christine, Delie Florence, Petignat Patrick
Department of Gynecology-Obstetrics, faculty of medicine, Geneva, Switzerland.
School of Pharmaceutical Sciences, University of Geneva, University of Lausanne, Geneva,Switzerland.
Oncoscience. 2014 Apr 30;1(4):262-71. doi: 10.18632/oncoscience.31. eCollection 2014.
Acellular fraction of ascites might play an active role in tumor development. Nevertheless the mechanisms involved in the tumor-modulating properties are still controversial. Here, we demonstrate that malignant ascites from 8 patients with epithelial ovarian cancer did not influence proliferative or invasive properties of ovarian cancer cells, but promoted H2O2-induced apoptosis and increased sensitivity to paclitaxel. Malignant ascites induced BRCA1, Fas and FasL expression and phosphorylation of JNK, but not the activation of caspase pathway. Ascites-induced apoptosis of ovarian cancer cells was strongly inhibited by a JNK inhibitor suggesting a critical role of JNK pathway in ascite-induced apoptosis. The use of siRNA JNK confirmed the importance of JNK in ascites-induced Fas and FasL expression. These results demonstrate that malignant ascites induce apoptosis of ovarian cancer cells and encourage us to think about the clinical management of ovarian cancer patients with malignant ascites.
腹水的无细胞部分可能在肿瘤发展中发挥积极作用。然而,参与肿瘤调节特性的机制仍存在争议。在此,我们证明,8例上皮性卵巢癌患者的恶性腹水并未影响卵巢癌细胞的增殖或侵袭特性,但促进了过氧化氢诱导的细胞凋亡并增加了对紫杉醇的敏感性。恶性腹水诱导了BRCA1、Fas和FasL的表达以及JNK的磷酸化,但未激活半胱天冬酶途径。JNK抑制剂强烈抑制腹水诱导的卵巢癌细胞凋亡,表明JNK途径在腹水诱导的细胞凋亡中起关键作用。使用siRNA JNK证实了JNK在腹水诱导的Fas和FasL表达中的重要性。这些结果表明,恶性腹水可诱导卵巢癌细胞凋亡,并促使我们思考恶性腹水卵巢癌患者的临床管理。