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Establishment and characterization of a cell line HCS1220 from human liver metastasis of colon cancer

机译:人结肠癌肝转移中HCS1220细胞系的建立与鉴定

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To establish one primary cell line of human liver metastasis of colon cancer. HCS1220 cell line was derived from one liver metastasis of colon cancer patient’s resected tumor sample. The characterization of the cell line was defined by karyotype analysis, short tandem repeat (STR) analysis and mycoplasma contamination. Subcutaneous injection 1?×?106?cells to four BALB/c nude mice, the viable tumors were developed and diagnosed (H&E staining). The expression of biomarkers CK20 and?CDX2 for colon cancer were determined by immunocytochemistry assay. HCS1220 cell line can grow stably and continuously passage. During the grow process, the contact loss in the growth process and superimposed growth, which could be defined as proliferation of malignant tumor. Chromosome analysis revealed the cells derived from human female. The cells were not contaminated by mycoplasma. By immunohistochemistry, the cell line was proven to express the biomarkers of colon cancer CK20 and CDX2, while a-fetoprotein, hep-1 and glypican-3 were stained negative, which demonstrated that the HCS1220 cell line originating from the intestinal tissue. HCS1220 cell line has the characteristics of primary human liver metastasis of colon cancer. The results of STR have?genetically showed that cell line is original, which can provided cell materials for research in vitro and can also help for establishing the mechanism model of liver metastasis of colon cancer and preparing, screening and evaluating anti-tumor drugs.
机译:建立一种人类结肠癌肝转移原代细胞。 HCS1220细胞系源自结肠癌患者切除的肿瘤样本的一种肝转移。通过核型分析,短串联重复序列(STR)分析和支原体污染来定义细胞系的特征。皮下注射1××106个细胞到四只BALB / c裸鼠中,发现并诊断了存活的肿瘤(H&E染色)。用免疫细胞化学法测定结肠癌的生物标志物CK20和ΔCDX2的表达。 HCS1220细胞系可以稳定生长并持续传代。在生长过程中,生长过程中的接触损失和重叠生长,可以定义为恶性肿瘤的增殖。染色体分析揭示了源自人类女性的细胞。细胞未被支原体污染。通过免疫组织化学,证明该细胞系表达结肠癌CK20和CDX2的生物标志物,而甲胎蛋白,hep-1和glypican-3被染色为阴性,这表明HCS1220细胞系起源于肠组织。 HCS1220细胞系具有原发性人类结肠癌肝转移的特征。 STR结果从遗传上证明细胞系是原始的,可以为体外研究提供细胞材料,也可以帮助建立结肠癌肝转移的机理模型,并制备,筛选和评价抗肿瘤药物。

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