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MOC31PE immunotoxin – targeting peritoneal metastasis from epithelial ovarian cancer

机译:MOC31PE免疫毒素–靶向上皮性卵巢癌的腹膜转移

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摘要

Peritoneal metastasis (PM) is an important feature of epithelial ovarian cancer (EOC) and is a frequent site of drug resistant disease recurrence, identifying PM-EOC an important clinical challenge. The MOC31PE immunotoxin targets and kills tumor cells expressing the epithelial cell adhesion molecule (EpCAM), which is highly expressed in EOC, and MOC31PE is being investigated for use in treatment of PM-EOC.The efficacy of MOC31PE treatment alone and in combination with cytotoxic drugs was investigated in two human EpCAM expressing EOC cell lines, B76 and MDHA-2774, in vitro and in corresponding mouse models mimicking PM-EOC. MOC31PE efficaciously killed tumor cells alone and showed equal or superior activity in vitro (paclitaxel, cisplatin, carboplatin) and in vivo (paclitaxel, mitomycin C) compared to the investigated cytotoxic drugs. Additive, or importantly, no antagonistic effects were observed in combination experiments.In ex vivo cell culture, the cytotoxic effect of MOC31PE was studied on freshly isolated surgical EOC samples. All investigated fresh EOC samples expressed EpCAM and MOC31PE effectively reduced cell viability in ex vivo cultures.In conclusion, these results, together with our previous preclinical and clinical experience, support development of MOC31PE for treatment of PM-EOC in combination with currently used cytotoxic drugs.
机译:腹膜转移(PM)是上皮性卵巢癌(EOC)的重要特征,并且是耐药性疾病复发的常见部位,因此确定PM-EOC是一项重要的临床挑战。 MOC31PE免疫毒素靶向并杀死表达在EOC中高度表达的上皮细胞粘附分子(EpCAM)的肿瘤细胞,并且正在研究MOC31PE用于治疗PM-EOC.MOC31PE单独治疗或与细胞毒性联合治疗的功效在体外和模拟PM-EOC的相应小鼠模型中,在两种表达人EpCAM的EOC细胞系B76和MDHA-2774中研究了这些药物。与研究的细胞毒性药物相比,MOC31PE单独有效地杀死了肿瘤细胞,并在体外(紫杉醇,顺铂,卡铂)和体内(紫杉醇,丝裂霉素C)表现出相同或更高的活性。在组合实验中未观察到加性或重要的拮抗作用。在离体细胞培养中,研究了MOC31PE对新鲜分离的手术EOC样品的细胞毒性作用。所有调查过的新鲜EOC样品均表达EpCAM和MOC31PE有效降低了离体培养中的细胞活力。总而言之,这些结果与我们之前的临床前和临床经验一起,支持开发MOC31PE与目前使用的细胞毒性药物联合治疗PM-EOC 。

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