Department of Experimental Pathology, Mayo Clinic College of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
PLoS One. 2013;8(1):e54578. doi: 10.1371/journal.pone.0054578. Epub 2013 Jan 31.
Ovarian cancer (OvCa) is the fifth most common cause of death from all cancers among women in United Sates and the leading cause of death from gynecological malignancies. While most OvCa patients initially respond to surgical debulking and chemotherapy, 75% of patients later succumb to the disease. Thus, there is an urgent need to test novel therapeutic agents to counteract the high mortality rate associated with OvCa. In this context, we have developed and engineered Nanoceria (NCe), nanoparticles of cerium oxide, possessing anti-oxidant properties, to be used as a therapeutic agent in OvCa. We show for the first time that NCe significantly inhibited production of reactive oxygen species (ROS) in A2780 cells, attenuated growth factor (SDF1, HB-EGF, VEGF(165) and HGF) mediated cell migration and invasion of SKOV3 cells, without affecting the cell proliferation. NCe treatment also inhibited VEGF(165) induced proliferation, capillary tube formation, activation of VEGFR2 and MMP2 in human umbilical vascular endothelial cells (HUVEC). NCe (0.1 mg/kg body weigh) treatment of A2780 ovarian cancer cells injected intra-peritoneally in nude mice showed significant reduction (p<0.002) in tumor growth accompanied by decreased tumor cell proliferation as evident from reduced tumor size and Ki67 staining. Accumulation of NCe was found in tumors isolated from treated group using transmission electron microscopy (TEM) and inductively coupled plasma mass spectroscopy (ICP-MS). Reduction of the tumor mass was accompanied by attenuation of angiogenesis, as observed by reduced CD31 staining and specific apoptosis of vascular endothelial cells. Collectively, these results indicate that cerium oxide based NCe is a novel nanoparticle that can potentially be used as an anti-angiogenic therapeutic agent in ovarian cancer.
卵巢癌(OvCa)是美国女性因癌症死亡的第五大常见原因,也是妇科恶性肿瘤死亡的主要原因。虽然大多数 OvCa 患者最初对手术去瘤和化疗有反应,但 75%的患者最终会死于该疾病。因此,迫切需要测试新的治疗药物来对抗与 OvCa 相关的高死亡率。在这种情况下,我们已经开发和设计了纳米氧化铈(NCe),这是一种具有抗氧化特性的氧化铈纳米颗粒,可用作 OvCa 的治疗剂。我们首次表明,NCe 可显著抑制 A2780 细胞中活性氧(ROS)的产生,减弱生长因子(SDF1、HB-EGF、VEGF(165)和 HGF)介导的 SKOV3 细胞迁移和侵袭,而不影响细胞增殖。NCe 处理还抑制了 VEGF(165)诱导的人脐静脉内皮细胞(HUVEC)增殖、毛细血管形成、VEGFR2 和 MMP2 的激活。NCe(0.1 mg/kg 体重)治疗在裸鼠体内腹腔注射 A2780 卵巢癌细胞,肿瘤生长明显减少(p<0.002),肿瘤细胞增殖减少,肿瘤体积缩小,Ki67 染色减少。使用透射电子显微镜(TEM)和电感耦合等离子体质谱(ICP-MS)在治疗组分离的肿瘤中发现 NCe 的积累。肿瘤质量的减少伴随着血管生成的减弱,这可以通过减少 CD31 染色和血管内皮细胞的特异性凋亡来观察到。总之,这些结果表明,基于氧化铈的 NCe 是一种新型纳米颗粒,可作为卵巢癌的新型抗血管生成治疗剂。