Scribner Kelly C, Wellberg Elizabeth A, Metz Richard P, Porter Weston W
Department of Integrative Biosciences, College of Veterinary Medicine, Texas A&M University, College Station, Texas 77843-4458, USA.
Mol Endocrinol. 2011 Apr;25(4):635-44. doi: 10.1210/me.2010-0423. Epub 2011 Feb 3.
Postlactational involution of the mammary gland provides a unique model to study breast cancer susceptibility and metastasis. We have shown that the short isoform of Singleminded-2s (Sim2s), a basic helix loop helix/PAS transcription factor, plays a role in promoting lactogenic differentiation, as well as maintaining mammary epithelial differentiation and malignancy. Sim2s is dynamically expressed during mammary gland development, with expression peaking during lactation, and decreasing in early involution. To determine the role of SIM2S in involution, we used transgenic mice expressing SIM2S under the mouse mammary tumor virus-Sim2s promoter. Overexpression of Sim2s in the mouse mammary gland resulted in delayed involution, indicated by a lower proportion of cleaved caspase-3-positive cells and slower reestablishment of the mammary fat pad. Immunohistochemical and quantitative RNA analysis showed a decrease in apoptotic markers and inflammatory response genes, and an increase in antiapoptotic genes, which were accompanied by inhibition of signal transducer and activator of transcription 3 activity. Microarray analysis confirmed that genes in the signal transducer and activator of transcription 3 signaling pathway were repressed by SIM2S expression, along with nuclear factor-κB and other key pathways involved in mammary gland development. Multiparous mouse mammary tumor virus-Sim2s females displayed a more differentiated phenotype compared with wild-type controls, characterized by enhanced β-casein expression and alveolar structures. Together, these results suggest a role for SIM2S in the normal involuting gland and identify potential downstream pathways regulated by SIM2S.
哺乳期后乳腺退化提供了一个研究乳腺癌易感性和转移的独特模型。我们已经表明,单 minded-2s(Sim2s)的短异构体,一种基本的螺旋-环-螺旋/PAS转录因子,在促进泌乳分化以及维持乳腺上皮分化和恶性肿瘤方面发挥作用。Sim2s在乳腺发育过程中动态表达,在泌乳期表达达到峰值,在早期退化时下降。为了确定SIM2S在退化中的作用,我们使用了在小鼠乳腺肿瘤病毒-Sim2s启动子下表达SIM2S的转基因小鼠。小鼠乳腺中Sim2s的过表达导致退化延迟,表现为裂解的caspase-3阳性细胞比例较低以及乳腺脂肪垫的重建较慢。免疫组织化学和定量RNA分析显示凋亡标志物和炎症反应基因减少,抗凋亡基因增加,同时信号转导和转录激活因子3活性受到抑制。微阵列分析证实,信号转导和转录激活因子3信号通路中的基因被SIM2S表达所抑制,同时核因子-κB和其他参与乳腺发育的关键通路也受到抑制。与野生型对照相比,多胎小鼠乳腺肿瘤病毒-Sim2s雌性表现出更分化的表型,其特征在于β-酪蛋白表达增强和肺泡结构。总之,这些结果表明SIM2S在正常退化的腺体中发挥作用,并确定了由SIM2S调节的潜在下游通路。