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Sorting and biological characteristics analysis for side population cells in human primary hepatocellular carcinoma

机译:人原发性肝细胞癌侧群细胞的分选和生物学特性分析

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Hepatocellular carcinoma (HCC) is the fifth most common cause of the tumor worldwide, its incidence is increasing year by year. This study aims to investigate the sorting and biological characteristics of side population (SP) cells. Human HCC tissues used were obtained from patients undergoing surgical resection. SP cells were sorted using flow cytometry. Cell cycle assay, apoptosis assay and colony formation assay were performed to detect cell proliferation and apoptosis. Invasion assay was employed to examine SP cell invasion. Tumorigenicity assay was used to evaluate tumorigenicity. HCC related microRNAs (miRNA) were analyzed using Micro-array analysis. Target genes were predicted using miRNA database. GO analsis was employed to predict target gene function. Apoptosis percentage was lower and cell viability was higher in SP cells than non-SP (NSP) cells. Colony forming ability of SP cells was significantly higher than NSP cells. Transwell assay positive cells in SP cells were higher significantly than NSP cells. Tumorigenicity of SP cells was higher significantly than NSP cells. 107 differentially expression miRNA were discovered, including 45 up-expressed miRNAs and 62 down-expressed miRNAs in SP cells. Up-regulated hsa-miR-193b-3p and hsa-miR-505-3p predict 25 and 35 target genes, and correlated with 4 and 42 GO terms, respectively. Down-regulated hsa-miR-200a-3p, hsa-miR-194-5p, hsa-miR-130b-3p predict 133, 48 and 127 target genes, and correlate with 10, 7 and 109 GO terms, respectively. In conclusion, proliferation, colony formation, anti-apoptosis, self-renewal capavility, invasive characteristic and tumorigenicity in SP cells isolated from HCC tissues was higher compared to NSP cells. Therefore, sorted SP cells could characterize with biological functions of cancer stem cells.
机译:肝细胞癌(HCC)是全球第五大最常见的肿瘤原因,其发病率逐年增加。这项研究旨在调查侧种群(SP)细胞的分类和生物学特性。使用的人肝癌组织取自接受手术切除的患者。使用流式细胞仪对SP细胞进行分选。进行细胞周期测定,凋亡测定和集落形成测定以检测细胞增殖和凋亡。侵袭测定用于检查SP细胞侵袭。致瘤性分析用于评估致瘤性。使用微阵列分析法分析了HCC相关的microRNA(miRNA)。使用miRNA数据库预测靶基因。 GO分析被用于预测靶基因功能。与非SP(NSP)细胞相比,SP细胞的凋亡百分比更低,细胞活力更高。 SP细胞的集落形成能力显着高于NSP细胞。 SP细胞中的Transwell分析阳性细胞显着高于NSP细胞。 SP细胞的致瘤性显着高于NSP细胞。在SP细胞中发现了107个差异表达的miRNA,包括45个上表达的miRNA和62个下表达的miRNA。上调的hsa-miR-193b-3p和hsa-miR-505-3p预测25和35个靶基因,分别与4和42个GO项相关。下调的hsa-miR-200a-3p,hsa-miR-194-5p,hsa-miR-130b-3p预测133、48和127个靶基因,并分别与10、7和109个GO项相关。总之,与NSP细胞相比,从HCC组织分离的SP细胞的增殖,集落形成,抗凋亡,自我更新能力,侵袭性和致瘤性更高。因此,分选的SP细胞可以表征癌症干细胞的生物学功能。

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