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双调蛋白在小鼠乳腺中诱导导管形态发生和小叶增生。

Induction of ductal morphogenesis and lobular hyperplasia by amphiregulin in the mouse mammary gland.

作者信息

Kenney N J, Smith G H, Rosenberg K, Cutler M L, Dickson R B

机构信息

Lombardi Cancer Center, Georgetown University, Washington, DC 20007, USA.

出版信息

Cell Growth Differ. 1996 Dec;7(12):1769-81.

PMID:8959346
Abstract

As the juvenile mouse mammary gland matures, it undergoes extensive epithelial proliferation, leading to a network of ductal branching that transverses the organ. Recent evidence suggests that the epidermal growth factor-related peptide amphiregulin (AR) may play multiple roles in the proliferation, differentiation, and neoplastic conversion of the mouse mammary gland. Using a dual approach of recombinant AR in slow-release pellets and retroviral expression of AR, we explored the roles of this growth factor in the mouse mammary gland in vivo. We first noted that recombinant AR can reestablish longitudinal ductal proliferation in growth quiescent mammary glands of ovariectomized mice. Furthermore, retrovirally transduced mammary transplants overexpressing AR developed into hyperplastic tertiary ducts and hyperplastic lobules with increased lateral branching, apparent 9 weeks after transplantation into cleared mammary fat pads. This is the first study to demonstrate that AR can reestablish the early developmental activity of ductal mammary epithelium and induce hyperplasia in vivo. These data, coupled with previous findings that demonstrated nearly universal overexpression of AR in human breast cancer and rodent mammary tumorigenesis, suggest that AR may be an important intermediary in glandular maturation and early malignant progression.

摘要

随着幼年小鼠乳腺的成熟,它会经历广泛的上皮细胞增殖,形成一个贯穿整个器官的导管分支网络。最近的证据表明,表皮生长因子相关肽双调蛋白(AR)可能在小鼠乳腺的增殖、分化和肿瘤转化中发挥多种作用。我们采用缓释微丸中的重组AR和AR的逆转录病毒表达这两种方法,在体内探索了这种生长因子在小鼠乳腺中的作用。我们首先注意到,重组AR可以在去卵巢小鼠的静止乳腺中重新建立纵向导管增殖。此外,过表达AR的逆转录病毒转导的乳腺移植在移植到清除的乳腺脂肪垫中9周后,发展为增生性三级导管和增生性小叶,侧支分支增加。这是第一项证明AR可以在体内重新建立乳腺导管上皮的早期发育活性并诱导增生的研究。这些数据,再加上之前证明AR在人类乳腺癌和啮齿动物乳腺肿瘤发生中几乎普遍过表达的研究结果,表明AR可能是腺体成熟和早期恶性进展的重要中介。

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