Department of Animal Science, University of Illinois at Urbana-Champaign, Urbana, IL, USA.
Methods Mol Biol. 2022;2424:189-198. doi: 10.1007/978-1-0716-1956-8_13.
Being able to accurately model metastasis is an important tool in cancer research. Several in vitro and ex vivo models have been developed to model metastasis from the ovary to the omentum, the most frequent metastatic site after leaving the ovary. However, the recent discovery that high-grade serous ovarian cancer (HGSOC) can originate in the fallopian tube and then metastasize to the ovary has necessitated the development of assays that can quantify the adhesion of tumor cells to the ovary. Here we describe a protocol for accessing the adhesion of fluorescent cells to mouse ovaries. This assay can be used to investigate the role of ovarian function, hormones, and adhesion molecules in metastasis of cancer cells originating in the fallopian tube to the ovary, an important step in the progression of HGSOC.
能够准确地模拟转移是癌症研究的重要工具。已经开发了几种体外和离体模型来模拟卵巢转移到网膜,这是卵巢离开后最常见的转移部位。然而,最近发现高级别浆液性卵巢癌(HGSOC)可能起源于输卵管,然后转移到卵巢,这就需要开发能够定量肿瘤细胞与卵巢粘附的检测方法。在这里,我们描述了一种访问荧光细胞与小鼠卵巢粘附的方案。该检测方法可用于研究卵巢功能、激素和粘附分子在输卵管来源的癌细胞转移到卵巢中的作用,这是 HGSOC 进展的重要步骤。