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The transforming activity of Wnt effectors correlates with their ability to induce the accumulation of mammary progenitor cells

机译:Wnt效应子的转化活性与其诱导乳腺祖细胞积累的能力有关

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摘要

Ectopic activation of the Wnt signaling pathway is highly oncogenic for many human tissues. Here, we show that ectopic Wnt signaling increases the effective stem cell activity in mouse mammary glands in vivo. Furthermore, Wnt effectors induce the accumulation of mouse mammary epithelial progenitors (assayed by Hoechst dye exclusion, a surrogate stem cell marker, side population cells) both in vivo and in vitro. The longevity of stem cells makes them good candidate tumor precursors, and we propose that Wnt-induced progenitor amplification is likely to be key to tumor initiation. In support of this notion, mammary glands from a tumor-resistant strain of mice (carrying a null mutation in syndecan-1) contain fewer side population cells. When this strain is crossed to mice that overexpress effectors of the β-catenin/T cell factor Wnt pathway, the amplification of progenitors is reduced, together with all subsequent events of tumor development. We propose that the growth dynamic of the stem cell fraction is a major determinant of tumor susceptibility.
机译:Wnt信号通路的异位激活对许多人体组织而言是高度致癌的。在这里,我们显示异位Wnt信号增加体内小鼠乳腺中的有效干细胞活性。此外,Wnt效应子在体内和体外均可诱导小鼠乳腺上皮祖细胞的积累(通过Hoechst染料排除,替代干细胞标记,侧群细胞测定)。干细胞的寿命使其成为良好的候选肿瘤前体,我们提出Wnt诱导的祖细胞扩增可能是肿瘤起始的关键。为了支持这一观点,来自抗肿瘤小鼠品系的乳腺(在syndecan-1中携带无效突变)包含的侧群细胞较少。当该菌株与过表达β-catenin/ T细胞因子Wnt途径效应子的小鼠杂交时,祖细胞的扩增以及所有随后的肿瘤发展事件都会减少。我们建议干细胞部分的生长动力学是肿瘤易感性的主要决定因素。

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