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Comparative Analysis of Protein Expression Concomitant with DNA Methyltransferase 3A Depletion in a Melanoma Cell Line
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作者 Xiaoyan Liu Shengnan Tang +5 位作者 Tonghua Li Haoyue Wang Jiangming Sun Qian Qiao Jun Yao Jian Fei 《American Journal of Analytical Chemistry》 2011年第5期539-572,共34页
DNA methyltransferase 3A (Dnmt3a), a de novo methyltransferase, has attracted a great deal of attention for its important role played in tumorigenesis. We have previously demonstrated that melanoma is unable to grow i... DNA methyltransferase 3A (Dnmt3a), a de novo methyltransferase, has attracted a great deal of attention for its important role played in tumorigenesis. We have previously demonstrated that melanoma is unable to grow in-vivo in conditions of Dnmt3a depletion in a mouse model. In this study, we cultured the Dnmt3a depletion B16 melanoma (Dnmt3a-D) cell line to conduct a comparative analysis of protein expression con-comitant with Dnmt3a depletion in a melanoma cell line. After two-dimensional separation, by gel electro-phoresis and liquid chromatography, combined with mass spectrometry analysis (1DE-LC-MS/MS), the re-sults demonstrated that 467 proteins were up-regulated and 535 proteins were down-regulated in the Dnmt3a-D cell line compared to the negative control (NC) cell line. The Genome Ontology (GO) and KEGG pathway were used to further analyze the altered proteins. KEGG pathway analysis indicated that the MAPK signaling pathway exhibited a greater alteration in proteins, an interesting finding due to the close relation-ship with tumorigenesis. The results strongly suggested that Dnmt3a potentially controls the process of tu-morigenesis through the regulation of the proteins (JNK1, p38α, ERK1, ERK2, and BRAF) involved in tu-mor-related pathways, such as the MAPK signaling pathway and melanoma pathway. 展开更多
关键词 Dnmt3a MELANOMA cell line 1DE-LC-MS/MS mapk signaling pathway MELANOMA pathway
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青石棉诱导A549细胞ERK1/2及Elk1激活的研究 被引量:4
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作者 王新朝 吴逸明 +2 位作者 李卓炜 James M.Samet Andrew J.Ghio 《卫生研究》 CAS CSCD 北大核心 2004年第4期398-399,共2页
目的 研究细胞外信号调节蛋白在青石棉致肺部疾病的作用。方法 用Western免疫印迹、免疫沉淀等对石棉刺激A5 4 9细胞后细胞外信号调节蛋白及其下游Elk1蛋白磷酸化等进行了研究。结果 石棉刺激细胞后 ,磷酸化ERK1 2、Elk1等高表达 ,... 目的 研究细胞外信号调节蛋白在青石棉致肺部疾病的作用。方法 用Western免疫印迹、免疫沉淀等对石棉刺激A5 4 9细胞后细胞外信号调节蛋白及其下游Elk1蛋白磷酸化等进行了研究。结果 石棉刺激细胞后 ,磷酸化ERK1 2、Elk1等高表达 ,差异有显著性 (P <0 0 5 )。结论 ERK1 2。 展开更多
关键词 青石棉 a549细胞 mapk信号传导
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