Crncec Ilija, Pathria Paulina, Svinka Jasmin, Eferl Robert
Institute of Cancer Research (ICR) & Comprehensive Cancer Center (CCC), Medical University Vienna, Borschkegasse 8a, 1090, Vienna, Austria.
Methods Mol Biol. 2015;1267:145-64. doi: 10.1007/978-1-4939-2297-0_7.
Colorectal cancer (CRC) originates from the epithelial cells lining the colon or rectum of the gastrointestinal tract and represents the third most common form of cancer worldwide. CRC is frequently associated with Colitis Ulcerosa or Crohn's Disease demonstrating the tumor-promoting role of inflammation. Colorectal tumor cells establish heterotypic interactions with inflammatory cells and cancer-associated fibroblasts in the tumor stroma that support tumor angiogenesis and are essential for tumor progression. Therefore, establishment of suitable mouse models mimicking the inflammatory etiology of CRC is important. Here we describe methods to induce CRC in mice, to quantify tumor parameters (multiplicity, tumor load, mean tumor size), and to analyze the cellular composition of the CRC tumor stroma.
结直肠癌(CRC)起源于胃肠道结肠或直肠的上皮细胞,是全球第三大常见癌症形式。CRC常与溃疡性结肠炎或克罗恩病相关,表明炎症具有促进肿瘤的作用。结直肠肿瘤细胞与肿瘤基质中的炎性细胞和癌症相关成纤维细胞建立异型相互作用,这些相互作用支持肿瘤血管生成,对肿瘤进展至关重要。因此,建立模拟CRC炎症病因的合适小鼠模型很重要。在此,我们描述了在小鼠中诱导CRC、量化肿瘤参数(数量、肿瘤负荷、平均肿瘤大小)以及分析CRC肿瘤基质细胞组成的方法。