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利用基因表达阵列阐明催乳素功能背后的转录谱。

Using gene expression arrays to elucidate transcriptional profiles underlying prolactin function.

作者信息

Gass Sandra, Harris Jessica, Ormandy Chris, Brisken Cathrin

机构信息

Swiss Institute for Experimental Cancer Research, National Center of Competence in Research Molecular Oncology, Epalinges s/Lausanne, Switzerland.

出版信息

J Mammary Gland Biol Neoplasia. 2003 Jul;8(3):269-85. doi: 10.1023/b:jomg.0000010029.85796.63.

Abstract

Prolactin is an ancient hormone, with different functions in many species. The binding of prolactin to its receptor, a member of the cytokine receptor superfamily, results in the activation of different intracellular signaling pathways, such as JAK2/STAT5, MAP kinase, and PI3K/AKT. How prolactin elicits so many different biological responses remains unclear. Recently, microarray technology has been applied to identify prolactin target genes in different systems. Here, we attempt to summarize and compare the available data. Our comparison of the genes reported to be transcriptionally regulated by prolactin indicates that there are few genes in common between the different tissues. Among the organs studied, mammary and prostate glands displayed the largest number of overlaps in putative prolactin target genes. Some of the candidates have been implicated in tumorigenesis. The relevance and validation of microarray data, as well as comparison of the results obtained by different groups, will be discussed.

摘要

催乳素是一种古老的激素,在许多物种中具有不同的功能。催乳素与其受体(细胞因子受体超家族的成员)结合,会导致不同的细胞内信号通路被激活,如JAK2/STAT5、丝裂原活化蛋白激酶(MAP激酶)和磷脂酰肌醇-3激酶/蛋白激酶B(PI3K/AKT)。催乳素如何引发如此多不同的生物学反应仍不清楚。最近,微阵列技术已被应用于识别不同系统中的催乳素靶基因。在此,我们试图总结和比较现有数据。我们对据报道受催乳素转录调控的基因进行的比较表明,不同组织之间几乎没有共同的基因。在所研究的器官中,乳腺和前列腺在假定的催乳素靶基因中显示出最大数量的重叠。一些候选基因与肿瘤发生有关。将讨论微阵列数据的相关性和验证,以及不同研究小组所得结果的比较。

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