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ER|[alpha]||[ndash]|CITED1 co-regulated genes expressed during pubertal mammary gland development: implications for breast cancer prognosis

机译:ER |α|| ndash | CITED1调控的基因在青春期乳腺发育过程中表达:对乳腺癌预后的影响

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Expression microarray analysis identified over 930 genes regulated during puberty in the mouse mammary gland. Most prominent were genes whose expression increased in parallel with pubertal development and remained high thereafter. Members of the Wnt, transforming growth factor- and oestrogen-signalling pathways were significantly overrepresented. Comparison to expression data from CITED1 knockout mice identified a subset of oestrogen-responsive genes displaying altered expression in the absence of CITED1. Included in this subset are stanniocalcin2 (Stc2) and amphiregulin (Areg). Chromatin immunoprecipitation revealed that ER binds to oestrogen response elements in both the Stc2 and Areg genes in the mammary gland during puberty. Additionally, CITED1 and ER localize to the same epithelial cells of the pubertal mammary gland, supporting a role for interaction of these two proteins during normal development. In a human breast cancer data set, expression of Stc2, Areg and CITED1 parallel that of ER. Similar to ER, CITED1 expression correlates with good outcome in breast cancer, implying that potential maintenance of the ER–CITED1 co-regulated signalling pathway in breast tumours can indicate good prognosis.
机译:表达微阵列分析确定了小鼠乳腺青春期期间调控的930多个基因。最突出的是其表达与青春期发育平行增加并且此后保持高水平的基因。 Wnt的成员,转化生长因子和雌激素信号通路明显过多。与来自CITED1基因敲除小鼠的表达数据进行比较,确定了在没有CITED1的情况下显示改变表达的一部分雌激素反应基因。此亚群中包括斯坦钙蛋白2(Stc2)和双调蛋白(Areg)。染色质的免疫沉淀表明,在青春期,ER与乳腺Stc2和Areg基因中的雌激素反应元件结合。此外,CITED1和ER定位在青春期乳腺的相同上皮细胞中,在正常发育过程中支持了这两种蛋白质相互作用的作用。在人类乳腺癌数据集中,Stc2,Areg和CITED1的表达与ER的表达平行。与ER相似,CITED1的表达与乳腺癌的良好预后相关,这暗示着ER-CITED1共同调节的乳腺癌信号通路的潜在维持可能预示良好的预后。

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