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首页> 外文期刊>Endocrinology >Paracrine-acting adiponectin promotes mammary epithelial differentiation and synergizes with genistein to enhance transcriptional response to estrogen receptor beta signaling.
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Paracrine-acting adiponectin promotes mammary epithelial differentiation and synergizes with genistein to enhance transcriptional response to estrogen receptor beta signaling.

机译:旁分泌作用的脂联素促进乳腺上皮分化,并与染料木黄酮协同作用,以增强对雌激素受体β信号转导的转录反应。

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摘要

Mammary stromal adipocytes constitute an active site for the synthesis of the adipokine, adiponectin (APN) that may influence the mammary epithelial microenvironment. The relationship between "local," mammary tissue-derived APN and breast cancer risk is poorly understood. Here, we identify a novel mechanism of APN-mediated signaling that influences mammary epithelial cell proliferation, differentiation, and apoptosis to modify breast cancer risk. We demonstrate that early dietary exposure to soy protein isolate induced mammary tissue APN production without corresponding effects on systemic APN levels. In estrogen receptor (ER)-negative MCF-10A cells, recombinant APN promoted lobuloalveolar differentiation by inhibiting oncogenic signal transducer and activator of transcription 3 activity. In ER-positive HC11 cells, recombinant APN increased ERbeta expression, inhibited cell proliferation, and induced apoptosis. Using the estrogen-responsive 4X-estrogen response element promoter-reporter construct to assess ER transactivation and small interfering RNA targeting of ERalpha and ERbeta, we show that APN synergized with the soy phytoestrogen genistein to promote ERbeta signaling in the presence of estrogen (17beta-estradiol) and ERbeta-specific agonist 2,3-bis(4-hydroxyphenyl)-propionitrile and to oppose ERalpha signaling in the presence of the ERalpha-specific agonist 4,4',4'-(4-propyl-(1H)-pyrazole-1,3,5-triyl)trisphenol. The enhancement of ERbeta signaling with APN + genistein cotreatments was associated with induction of apoptosis, increased expression of proapoptotic/prodifferentiation genes (Bad, p53, and Pten), and decreased antiapoptotic (Bcl2 and survivin) transcript levels. Our results suggest that mammary-derived APN can influence adjacent epithelial function by ER-dependent and ER-independent mechanisms that are consistent with reduction of breast cancer risk and suggest local APN induction by dietary factors as a targeted approach for promotion of breast health.
机译:乳腺基质脂肪细胞构成了可能影响乳腺上皮微环境的脂肪因子,脂联素(APN)合成的活性位点。人们对“局部”乳腺组织源性APN与乳腺癌风险之间的关系了解甚少。在这里,我们确定了影响乳腺上皮细胞增殖,分化和凋亡以修饰乳腺癌风险的APN介导信号传导的新机制。我们证明,早期饮食中接触大豆蛋白分离株会诱导乳腺组织APN的产生,而对全身APN水平没有相应的影响。在雌激素受体(ER)阴性的MCF-10A细胞中,重组APN通过抑制致癌信号转导子和转录激活因子3的活性,促进了肺泡的分化。在ER阳性HC11细胞中,重组APN可增加ERbeta表达,抑制细胞增殖并诱导凋亡。使用雌激素反应性4X雌激素反应元件启动子-报告基因构建体来评估ER反式激活和靶向ERalpha和ERbeta的小分子干扰RNA,我们显示APN与大豆植物雌激素染料木黄酮协同作用,在雌激素存在下促进ERbeta信号传导(17beta-雌二醇)和ERbeta特异性激动剂2,3-双(4-羟苯基)-丙腈,并在存在ERalpha特异性激动剂4,4',4'-(4-丙基-(1H)-吡唑-1,3,5-三基)三酚。 APN +金雀异黄素协同治疗增强ERbeta信号传导与细胞凋亡的诱导,促凋亡/促分化基因(Bad,p53和Pten)的表达增加以及抗凋亡(Bcl2和survivin)转录水平降低有关。我们的结果表明,乳腺源性APN可以通过ER依赖性和ER非依赖性机制影响邻近上皮功能,这与降低乳腺癌风险相一致,并建议通过饮食因素诱导局部APN作为促进乳房健康的一种有针对性的方法。

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