School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, GA 30332, USA.
Nanomedicine. 2010 Jun;6(3):399-408. doi: 10.1016/j.nano.2009.11.003. Epub 2009 Dec 5.
A majority of ovarian cancer metastases result from the shedding of malignant cells from the primary tumor into the abdominal cavity. Free-floating cancer cells in serous effusions of late-stage ovarian cancer patients may spread to internal organs, making effective treatment extremely difficult. Selective removal of ovarian cancer cells from serous fluids may abate metastasis and improve long-term prognoses. We have already shown that superparamagnetic nanoparticles conjugated to an ephrin-A1 mimetic peptide with a high affinity for the EphA2 receptor can be used to capture and remove cultured human ovarian cancer cells from the peritoneal of experimental mice. Here we demonstrate the potential clinical utility of the methodology by in vitro capture and isolation of cancer cells from the ascites fluid of ovarian cancer patients.
Ovarian cancer metastases usually are the result of shedding of malignant cells from the primary tumor into the abdominal cavity. In this paper, a novel nanotechnology-based method is demonstrated for the in vitro capture and isolation of cancer cells from the ascites fluid of ovarian cancer patients.
大多数卵巢癌转移是由于原发肿瘤中的恶性细胞脱落到腹腔中。晚期卵巢癌患者的浆膜性渗出液中的游离癌细胞可能会扩散到内部器官,使有效治疗变得极其困难。从浆膜液中选择性地去除卵巢癌细胞可能会阻止转移并改善长期预后。我们已经表明,与 EphA2 受体具有高亲和力的 Ephrin-A1 模拟肽偶联的超顺磁纳米粒子可用于从实验小鼠的腹膜腔中捕获和去除培养的人卵巢癌细胞。在这里,我们通过从卵巢癌患者的腹水体外捕获和分离癌细胞来证明该方法的潜在临床应用。
卵巢癌转移通常是由于原发肿瘤中的恶性细胞脱落到腹腔中。在本文中,展示了一种基于新型纳米技术的体外从卵巢癌患者的腹水中捕获和分离癌细胞的方法。