信号转导和转录激活因子5a影响乳腺上皮细胞存活和肿瘤发生。

R C Humphreys, L Hennighausen
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引用次数: 0

摘要

乳腺在哺乳结束时经历广泛的组织重塑和细胞死亡,这一过程被称为内化。我们提出的证据表明,催乳素激活的转录因子信号转导和转录激活因子5a (Stat5a)在乳腺退化过程中调控细胞死亡中起着至关重要的作用。在一个转化生长因子- α转基因小鼠模型中,显示出乳腺复旧延迟,Stat5a的缺失促进了乳腺形态学的复旧相关变化以及程序性细胞死亡的程度和时间。这些stat5a依赖性的变化也影响表皮生长因子受体引发的乳腺肿瘤发生。转化生长因子α转基因在乳腺上皮中的过度表达可再现性地产生乳腺增生和肿瘤。在活化的表皮生长因子受体存在的情况下,Stat5a的缺失将初始增生和乳腺肿瘤的发展延迟了6周。这些观察结果表明Stat5a是一种存活因子,它的存在是乳腺上皮抵抗退化和复归介导的细胞凋亡所必需的。我们还认为Stat5a是一种先行的、局部作用的分子,它在退化过程中启动上皮细胞的退化和重组过程。
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Signal transducer and activator of transcription 5a influences mammary epithelial cell survival and tumorigenesis.

The mammary gland undergoes extensive tissue remodeling and cell death at the end of lactation in a process known as involution. We present evidence that the prolactin-activated transcription factor signal transducer and activator of transcription 5a (Stat5a) has a crucial role in the regulation of cell death during mammary gland involution. In a transforming growth factor-alpha transgenic mouse model that exhibited delayed mammary gland involution, the absence of Stat5a facilitated involution-associated changes in morphology of the gland and the extent and timing of programmed cell death. These Stat5a-dependent changes also affected epidermal growth factor receptor-initiated mammary gland tumorigenesis. Overexpression of the transforming growth factor alpha transgene in the mammary epithelium reproducibly generated mammary hyperplasia and tumors. In the presence of the activated epidermal growth factor receptor, deletion of Stat5a delayed initial hyperplasia and mammary tumor development by 6 weeks. These observations demonstrate that Stat5a is a survival factor, and its presence is required for the epithelium of the mammary gland to resist regression and involution-mediated apoptosis. We also suggest that Stat5a is one of the antecedent, locally acting molecules that initiate the process of epithelial regression and reorganization during involution.

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