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乳腺导管环境对于雌激素受体阳性(ER⁺)乳腺癌中雌激素信号的忠实维持是必要的。

Mammary Ductal Environment Is Necessary for Faithful Maintenance of Estrogen Signaling in ER⁺ Breast Cancer.

作者信息

Haricharan Svasti, Lei Jonathan, Ellis Matthew

机构信息

Department of Medicine, Baylor College of Medicine, Houston, TX 77030, USA.

Interdepartmental Program in Translational Biology and Molecular Medicine, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Cancer Cell. 2016 Mar 14;29(3):249-250. doi: 10.1016/j.ccell.2016.02.017.

DOI:10.1016/j.ccell.2016.02.017
PMID:26977876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5047062/
Abstract

In this issue of Cancer Cell, Sflomos et al. (2016) describe a robust preclinical animal model of ER⁺ breast cancer. The authors identify the critical role of the breast microenvironment in determining hormone response of ER⁺ breast cancer cells and in driving the luminal phenotype of breast cancer.

摘要

在本期《癌细胞》杂志中,斯弗洛莫斯等人(2016年)描述了一种强大的雌激素受体阳性(ER⁺)乳腺癌临床前动物模型。作者们确定了乳腺微环境在决定ER⁺乳腺癌细胞的激素反应以及推动乳腺癌管腔表型方面的关键作用。

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Mammary Ductal Environment Is Necessary for Faithful Maintenance of Estrogen Signaling in ER⁺ Breast Cancer.乳腺导管环境对于雌激素受体阳性(ER⁺)乳腺癌中雌激素信号的忠实维持是必要的。
Cancer Cell. 2016 Mar 14;29(3):249-250. doi: 10.1016/j.ccell.2016.02.017.
2
A Preclinical Model for ERα-Positive Breast Cancer Points to the Epithelial Microenvironment as Determinant of Luminal Phenotype and Hormone Response.一种 ERα 阳性乳腺癌的临床前模型指出,上皮微环境是决定腔面表型和激素反应的决定因素。
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Estrogen receptor beta growth-inhibitory effects are repressed through activation of MAPK and PI3K signalling in mammary epithelial and breast cancer cells.雌激素受体β的生长抑制作用通过 MAPK 和 PI3K 信号通路的激活在乳腺上皮细胞和乳腺癌细胞中受到抑制。
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Clin Cancer Res. 2000 Feb;6(2):512-8.
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Oncol Lett. 2019 Jan;17(1):1160-1166. doi: 10.3892/ol.2018.9668. Epub 2018 Nov 5.
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本文引用的文献

1
A Preclinical Model for ERα-Positive Breast Cancer Points to the Epithelial Microenvironment as Determinant of Luminal Phenotype and Hormone Response.一种 ERα 阳性乳腺癌的临床前模型指出,上皮微环境是决定腔面表型和激素反应的决定因素。
Cancer Cell. 2016 Mar 14;29(3):407-422. doi: 10.1016/j.ccell.2016.02.002. Epub 2016 Mar 3.
2
Endocrine-therapy-resistant ESR1 variants revealed by genomic characterization of breast-cancer-derived xenografts.通过对乳腺癌衍生异种移植物的基因组特征分析发现的内分泌治疗耐药 ESR1 变异体。
Cell Rep. 2013 Sep 26;4(6):1116-30. doi: 10.1016/j.celrep.2013.08.022. Epub 2013 Sep 19.
3
Mouse models of estrogen receptor-positive breast cancer.雌激素受体阳性乳腺癌的小鼠模型
J Carcinog. 2011;10:35. doi: 10.4103/1477-3163.91116. Epub 2011 Dec 22.
4
STAT1-deficient mice spontaneously develop estrogen receptor α-positive luminal mammary carcinomas.STAT1 缺陷型小鼠自发形成雌激素受体 α 阳性腔上皮型乳腺肿瘤。
Breast Cancer Res. 2012 Jan 20;14(1):R16. doi: 10.1186/bcr3100.
5
Introduction of oncogenes into mammary glands in vivo with an avian retroviral vector initiates and promotes carcinogenesis in mouse models.利用禽逆转录病毒载体将癌基因导入体内的乳腺,可在小鼠模型中引发并促进癌症发生。
Proc Natl Acad Sci U S A. 2006 Nov 14;103(46):17396-401. doi: 10.1073/pnas.0608607103. Epub 2006 Nov 7.
6
Biological and genetic properties of the p53 null preneoplastic mammary epithelium.p53基因缺失的乳腺肿瘤前上皮细胞的生物学和遗传学特性。
FASEB J. 2002 Jun;16(8):881-3. doi: 10.1096/fj.01-0885fje. Epub 2002 Apr 10.
7
Development of a flexible and specific gene delivery system for production of murine tumor models.用于构建小鼠肿瘤模型的灵活且特异性基因递送系统的开发。
Oncogene. 1999 Sep 20;18(38):5253-60. doi: 10.1038/sj.onc.1203087.
8
Mammary tumorigenesis in 7,12-dimethybenzanthracene-treated C57BL x DBA/2f F1 mice.7,12-二甲基苯并蒽处理的C57BL×DBA/2f F1小鼠的乳腺肿瘤发生
Cancer Res. 1980 Feb;40(2):368-73.