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Cyclophilin A function in mammary epithelium impacts Jak2/Stat5 signaling morphogenesis differentiation and tumorigenesis in the mammary gland

机译:亲环蛋白A在乳腺上皮中的功能影响乳腺中的Jak2 / Stat5信号转导形态发生分化和肿瘤发生

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摘要

The prolyl isomerase cyclophilin A (CypA) regulates the Jak2/Stat5 pathway, which is necessary for mammary differentiation and the pathogenesis of breast cancer. In this study, we assessed the role of this isomerase during mammary gland development and erbB2-driven tumorigenesis. Genetic deletion of CypA resulted in delayed mammary gland morphogenesis and differentiation with corresponding decrease in Jak2/Stat5 activation; mammary gland cross-transplantation confirmed this defect was epithelial in nature. Analysis of mammary stem and progenitor populations revealed significant disruption of epithelial maturation. Loss of CypA in the erbB2 transgenic mouse model revealed a marked increase in mammary tumor latency that correlated with decreased Stat5 activation, associated gene expression, and reduced epithelial cell proliferation. These results demonstrate an important role for CypA in the regulation of Jak2/Stat5-mediated biology in mammary epithelium, identifying this isomerase as a novel target for therapeutic intervention.
机译:脯氨酰异构酶亲环蛋白A(CypA)调节Jak2 / Stat5途径,这对于乳腺分化和乳腺癌的发病机制是必需的。在这项研究中,我们评估了这种异构酶在乳腺发育和erbB2驱动的肿瘤发生过程中的作用。 CypA的遗传删除导致延迟的乳腺形态发生和分化,并相应降低Jak2 / Stat5激活。乳腺交叉移植证实了该缺陷本质上是上皮的。乳腺干和祖细胞的分析显示上皮成熟的重大破坏。 erbB2转基因小鼠模型中CypA的缺失表明,乳腺肿瘤潜伏期显着增加,这与Stat5激活降低,相关基因表达减少以及上皮细胞增殖减少有关。这些结果表明,CypA在乳腺上皮细胞中调控Jak2 / Stat5介导的生物学过程中起着重要作用,从而将该异构酶鉴定为治疗干预的新靶标。

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