首页> 美国卫生研究院文献>Journal of Visualized Experiments : JoVE >Murine Experimental Model of Original Tumor Development and Peritoneal Metastasis via Orthotopic Inoculation with Ovarian Carcinoma Cells
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Murine Experimental Model of Original Tumor Development and Peritoneal Metastasis via Orthotopic Inoculation with Ovarian Carcinoma Cells

机译:通过卵巢癌细胞原位接种的原始肿瘤发展和腹膜转移的小鼠实验模型

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摘要

Epithelial ovarian carcinoma (EOC) is associated with a poor prognosis because it shows peritoneal dissemination. To improve the prognosis, it is important to control peritoneal dissemination. However, it is still unclear how tumor cells detach from primary lesions and attach to the mesothelium. The establishment of an appropriate animal model is needed to gain an understanding of the mechanism of peritoneal dissemination in vivo. In the current study, we introduce the process from the local injection of EOC cells into the murine ovarian surface to the development of metastasis, including the peritoneum and distant organs. Female nude mice (BALB/c nuu) at 8 weeks of age were used. Under a microscopic field of view, EOC cells (1 x 105 cells/µl of medium-extracellular matrix (ECM)-based hydrogel/unilateral ovary/mouse) were injected into murine ovaries through a retroperitoneal approach from the dorsal flank. This proposed method is a less invasive procedure for the mouse and minimizes damage to the ovary. Here, we describe the methodological steps in the development of the original and metastatic tumor formation of EOC.
机译:上皮性卵巢癌(EOC)表现为腹膜扩散,因此预后不良。为了改善预后,重要的是控制腹膜的扩散。然而,尚不清楚肿瘤细胞如何从原发性病变中分离并附着于间皮。需要建立适当的动物模型以了解体内腹膜扩散的机制。在当前的研究中,我们介绍了从EOC细胞局部注入鼠卵巢表面到包括腹膜和远处器官在内的转移发展的过程。使用8周龄的雌性裸鼠(BALB / c nu / nu)。在显微镜下,通过腹膜后方法将EOC细胞(1 x 10 5 细胞/ µl基于中细胞外基质(ECM)的水凝胶/单侧卵巢/小鼠)注入小鼠卵巢从背侧。该提议的方法对小鼠的侵入性较小,可最大程度地减少对卵巢的损害。在这里,我们描述了EOC原始和转移性肿瘤形成过程中的方法学步骤。

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