Suppr超能文献

与Smad3野生型小鼠相比,致癌物7,12-二甲基苯并[a]蒽诱导的Smad3杂合小鼠乳腺肿瘤发生加速。

Carcinogen 7,12-dimethylbenz[a]anthracene-induced mammary tumorigenesis is accelerated in Smad3 heterozygous mice compared to Smad3 wild type mice.

作者信息

Liu Zhengxue, Kundu-Roy Tanima, Matsuura Isao, Wang Guannan, Lin Yong, Lou You-Rong, Barnard Nicola J, Wang Xiao-Fan, Huang Mou-Tuan, Suh Nanjoo, Liu Fang

机构信息

Center for Advanced Biotechnology and Medicine, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.

Susan Lehman Cullman Laboratory for Cancer Research, Department of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.

出版信息

Oncotarget. 2016 Oct 4;7(40):64878-64885. doi: 10.18632/oncotarget.11713.

Abstract

Previous studies based on cell culture and xenograft animal models suggest that Smad3 has tumor suppressor function for breast cancer during early stages of tumorigenesis. In this report, we show that DMBA (7,12-dimethylbenz[a]anthracene), a chemical carcinogen, induces mammary tumor formation at a significantly higher frequency in the Smad3 heterozygous mice than in the Smad3 wild type mice. This is the first genetic evidence showing that Smad3 inhibits mammary tumor formation in a mouse model. Our findings support the notion that Smad3 has important tumor suppressor function for breast cancer.

摘要

以往基于细胞培养和异种移植动物模型的研究表明,Smad3在肿瘤发生的早期阶段对乳腺癌具有肿瘤抑制功能。在本报告中,我们发现化学致癌物7,12-二甲基苯并[a]蒽(DMBA)诱导Smad3杂合小鼠乳腺肿瘤形成的频率显著高于Smad3野生型小鼠。这是首个在小鼠模型中表明Smad3抑制乳腺肿瘤形成的遗传学证据。我们的研究结果支持Smad3对乳腺癌具有重要肿瘤抑制功能这一观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d282/5323122/1220fe749509/oncotarget-07-64878-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验