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Proteome of human colon cancer stem cells: A comparative analysis.

机译:人结肠癌干细胞蛋白质组:比较分析。

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AIM: To isolate and identify the biological characteristics of human colon cancer stem cells (SW1116 cells) and further study their proteome. METHODS: SW1116 cells were isolated and cultured with a serum-free medium (SFM). Sphere formation was assayed to observe the formation of colon cancer stem cell spheres. SW1116 cells were inoculated into a serum-containing medium for observing their differentiation characteristics. Proliferation curve and cross-resistance of SW1116 cells to different drugs were detected by MTT. Percentage of SP cells in SW1116 cells was detected with Hoechst33342 staining. Telomerase activity in SW1116cells was checked by polymerase chain reaction (PCR)-enzyme linked immunosorbent assay. Expressions of stem cell relevant genes and proteins were detected by reverse transcription-PCR and Western blot, respectively. Total protein was isolated from SW1116 cells by two-dimensional gel electrophoresis (2-DE) and differentially expressed proteins were identified by tandem mass spectrometry (MALDI-TOF/TOF). RESULTS: The isolated SW1116 cells presented as spheroid and suspension growths in SFM with a strong self-renewal, proliferation, differentiation and drug-resistance ability. The percentage of SP cells in SW1116 cells was 38.9%. The SW1116 cells co-expressed the CD133 and CD29 proteins. The telomerase activity in SW1116 cells was increased. The expressions of different stem cell relevant genes and proteins were detected. The proteomic analysis showed that the 26 protein spots were differently expressed in SW1116 cells and 10 protein spots were identified as ubiquitin fusion-degradation 1-like protein, nuclear chloride channel protein, tubulin beta, Raichu404X, stratifin, F-actin capping protein alpha-1 subunit, eukaryotic translation elongation factor 1 delta isoform 2, hypothetical protein, glyceraldehyde-3-phosphate dehydrogenase and guanine nucleotide binding protein beta polypeptide 2-like 1, respectively. CONCLUSION: SW1116 cells are biologically characterized by self-renewal, proliferation and differentiation, and the differently expressed proteins in SW1116 cells may be essential for isolating cancer stem cells.
机译:目的:分离和鉴定人结肠癌干细胞(SW1116)的生物学特性,并进一步研究其蛋白质组。方法:分离SW1116细胞并用无血清培养基(SFM)培养。测定球的形成以观察结肠癌干细胞球的形成。将SW1116细胞接种到含血清的培养基中以观察其分化特征。 MTT法检测SW1116细胞对不同药物的增殖曲线和交叉耐药性。用Hoechst33342染色检测SW1116细胞中SP细胞的百分比。通过聚合酶链反应(PCR)-酶联免疫吸附法检测SW1116细胞中的端粒酶活性。通过逆转录PCR和Western blot分别检测干细胞相关基因和蛋白质的表达。通过二维凝胶电泳(2-DE)从SW1116细胞中分离总蛋白,并通过串联质谱(MALDI-TOF / TOF)鉴定差异表达的蛋白。结果:分离的SW1116细胞在SFM中呈球状和悬浮状生长,具有很强的自我更新,增殖,分化和耐药性。 SW1116细胞中SP细胞的百分比为38.9%。 SW1116细胞共表达CD133和CD29蛋白。 SW1116细胞中的端粒酶活性增加。检测不同干细胞相关基因和蛋白质的表达。蛋白质组学分析显示,SW1116细胞中26个蛋白点表达不同,其中10个蛋白点被确认为泛素融合降解1样蛋白,核氯化物通道蛋白,微管蛋白beta,Raichu404X,stratifin,F-肌动蛋白加帽蛋白α- 1个亚基,真核翻译延伸因子1δ同工型2,假设蛋白,3-磷酸甘油醛脱氢酶和鸟嘌呤核苷酸结合蛋白β-多肽2-样1。结论:SW1116细胞具有自我更新,增殖和分化的生物学特性,SW1116细胞中不同表达的蛋白质可能对分离癌症干细胞至关重要。

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