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利用小鼠乳腺进行mILC研究:一种浸润性小叶癌模型

mILC-ing the mouse mammary gland: A model for invasive lobular carcinoma.

作者信息

Alvarez James V, Perez Denise, Chodosh Lewis A

机构信息

Department of Cancer Biology and Abramson Family Cancer Research Institute, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.

出版信息

Cancer Cell. 2006 Nov;10(5):347-9. doi: 10.1016/j.ccr.2006.10.016.

DOI:10.1016/j.ccr.2006.10.016
PMID:17097555
Abstract

Mouse models that faithfully recapitulate human cancers are indispensable tools for studying the molecular mechanisms of tumorigenesis and testing potential anticancer therapies. In this issue of Cancer Cell, Derksen et al. describe a new mouse model that mimics multiple features of invasive lobular carcinoma of the breast (ILC), a histological subtype of human breast cancer for which no mouse model currently exists. This model further reveals an important causal link between E-cadherin loss and tumor initiation and metastasis and, in doing so, provides a valuable entrée into the tumor-suppressive functions of E-cadherin as well as the molecular underpinnings of ILC.

摘要

能够忠实地重现人类癌症的小鼠模型是研究肿瘤发生分子机制和测试潜在抗癌疗法不可或缺的工具。在本期《癌细胞》杂志中,德克森等人描述了一种新的小鼠模型,该模型模拟了乳腺浸润性小叶癌(ILC)的多种特征,ILC是一种人类乳腺癌的组织学亚型,目前尚无小鼠模型。该模型进一步揭示了E-钙黏蛋白缺失与肿瘤起始和转移之间的重要因果关系,从而为E-钙黏蛋白的肿瘤抑制功能以及ILC的分子基础提供了有价值的切入点。

相似文献

1
mILC-ing the mouse mammary gland: A model for invasive lobular carcinoma.利用小鼠乳腺进行mILC研究:一种浸润性小叶癌模型
Cancer Cell. 2006 Nov;10(5):347-9. doi: 10.1016/j.ccr.2006.10.016.
2
Somatic inactivation of E-cadherin and p53 in mice leads to metastatic lobular mammary carcinoma through induction of anoikis resistance and angiogenesis.小鼠中E-钙黏蛋白和p53的体细胞失活通过诱导失巢凋亡抗性和血管生成导致转移性小叶乳腺癌。
Cancer Cell. 2006 Nov;10(5):437-49. doi: 10.1016/j.ccr.2006.09.013.
3
Mammary-specific inactivation of E-cadherin and p53 impairs functional gland development and leads to pleomorphic invasive lobular carcinoma in mice.乳腺特异性敲除 E-钙黏蛋白和 p53 会损害功能性乳腺发育,并导致小鼠多形性浸润性小叶癌。
Dis Model Mech. 2011 May;4(3):347-58. doi: 10.1242/dmm.006395. Epub 2011 Jan 31.
4
Modeling invasive lobular breast carcinoma by CRISPR/Cas9-mediated somatic genome editing of the mammary gland.通过CRISPR/Cas9介导的乳腺体细胞基因组编辑对浸润性小叶乳腺癌进行建模。
Genes Dev. 2016 Jun 15;30(12):1470-80. doi: 10.1101/gad.279190.116.
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Cadherins and the mammary gland.钙黏蛋白与乳腺
J Cell Biochem. 2005 Jun 1;95(3):488-96. doi: 10.1002/jcb.20419.
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αE-catenin is a candidate tumor suppressor for the development of E-cadherin-expressing lobular-type breast cancer.αE-连环蛋白是表达 E-钙黏蛋白的乳腺小叶型癌发生发展的候选肿瘤抑制因子。
J Pathol. 2018 Aug;245(4):456-467. doi: 10.1002/path.5099. Epub 2018 Jun 20.
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Synchronous squamous cell carcinoma of the breast and invasive lobular carcinoma.乳腺同步性鳞状细胞癌和浸润性小叶癌。
APMIS. 2007 Dec;115(12):1422-5. doi: 10.1111/j.1600-0463.2007.00878.x.
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Cadherins and catenins in breast cancer.乳腺癌中的钙黏蛋白和连环蛋白
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Lobular breast cancer: molecular basis, mouse and cellular models.小叶性乳腺癌:分子基础、小鼠模型和细胞模型
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PTEN Loss in E-Cadherin-Deficient Mouse Mammary Epithelial Cells Rescues Apoptosis and Results in Development of Classical Invasive Lobular Carcinoma.E-钙黏蛋白缺陷型小鼠乳腺上皮细胞中PTEN缺失可挽救细胞凋亡并导致经典浸润性小叶癌的发生。
Cell Rep. 2016 Aug 23;16(8):2087-2101. doi: 10.1016/j.celrep.2016.07.059. Epub 2016 Aug 11.

引用本文的文献

1
Synchronous Orbital and Gastrointestinal Metastases from Breast Cancer: A Case Report and Review of Literature.乳腺癌的同步眼眶和胃肠道转移:一例报告并文献复习
Case Rep Oncol Med. 2015;2015:282790. doi: 10.1155/2015/282790. Epub 2015 May 13.
2
Choosing a mouse model: experimental biology in context--the utility and limitations of mouse models of breast cancer.选择小鼠模型:背景下的实验生物学——乳腺癌小鼠模型的实用性和局限性。
Cold Spring Harb Perspect Biol. 2011 Sep 1;3(9):a009670. doi: 10.1101/cshperspect.a009670.
3
Mammary-specific inactivation of E-cadherin and p53 impairs functional gland development and leads to pleomorphic invasive lobular carcinoma in mice.
乳腺特异性敲除 E-钙黏蛋白和 p53 会损害功能性乳腺发育,并导致小鼠多形性浸润性小叶癌。
Dis Model Mech. 2011 May;4(3):347-58. doi: 10.1242/dmm.006395. Epub 2011 Jan 31.
4
Mouse N-acetyltransferase type 2, the homologue of human N-acetyltransferase type 1.小鼠N-乙酰基转移酶2,即人类N-乙酰基转移酶1的同源物。
Biochem Pharmacol. 2008 Apr 1;75(7):1550-60. doi: 10.1016/j.bcp.2007.12.012. Epub 2008 Jan 5.