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首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >Mitogen-activated protein kinase pathway is involved in α6 integrin gene expression in androgen-independent prostate cancer cells: role of proximal Sp1 consensus sequence
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Mitogen-activated protein kinase pathway is involved in α6 integrin gene expression in androgen-independent prostate cancer cells: role of proximal Sp1 consensus sequence

机译:丝裂原激活的蛋白激酶途径参与雄激素非依赖性前列腺癌细胞中的α6整合素基因表达:近端Sp1共有序列的作用

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Metastatic diseases of prostate cancer reveal high expression of α6 integrin and the activation of mitogen-activated protein kinases (MAP kinase). therefore, the present study was conducted to examine whether MAP kinase pathway is involved in the α6 integrin gene expression in androgen-independent prostate cancer cell lines. α6 integrin mRNA expression, the α6 integrin promoter-induced luciferase activities and MAP kinase enzyme activities in androgen-independent LNCaP and PC-3 cell liens were higher than those in androgen-dependent LNCaP. Deletion and mutation analysis showed that Sp1 consensus sequence at -48 to -43 bp from the transcription start site was necessary for basal promoter activity. Binding of Sp1 to its consensus sequence in three cell lines was confirmed by electrophoretic mobility shift assays. Sp1 binding to its consensus sequence, as well as promoter activity and mRNA expression, were found to be inhibited by an inhibitor of MAP kinase kinase 1 and 2, U0126, in the androgen-independent cell lines. Our results indicate that the proximal Sp1 is necessary for basal promoter activity of the α6 integrin, suggesting that signal transduction from MAP kinases to activation of Sp1 might be involved in α6 integrin gene expression in androgen-independent prostate cancer cell lines.
机译:前列腺癌的转移性疾病显示出高表达的α6整联蛋白和丝裂原激活的蛋白激酶(MAP激酶)的激活。因此,本研究旨在检查MAP激酶途径是否参与非雄激素依赖性前列腺癌细胞系中的α6整合素基因表达。雄激素非依赖性LNCaP和PC-3细胞株中α6整合素mRNA的表达,α6整合素启动子诱导的萤光素酶活性和MAP激酶活性高于雄激素依赖性LNCaP。缺失和突变分析表明,从转录起始位点开始在-48至-43bp处的Sp1共有序列对于基础启动子活性是必需的。通过电泳迁移率迁移测定法证实了Sp1在三个细胞系中与其共有序列的结合。发现在非雄激素非依赖性细胞系中,Sp1与其共有序列的结合以及启动子活性和mRNA表达受到MAP激酶1和2抑制剂U0126的抑制。我们的结果表明,近端Sp1对于α6整联蛋白的基础启动子活性是必需的,这表明从MAP激酶到Sp1激活的信号转导可能与雄激素非依赖性前列腺癌细胞系中的α6整联蛋白基因表达有关。

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