Suppr超能文献

青藤碱通过抑制 SHh 通路减少乳腺癌细胞的生长和转移,提高荷瘤小鼠的存活率。

Sinomenine reduces growth and metastasis of breast cancer cells and improves the survival of tumor-bearing mice through suppressing the SHh pathway.

机构信息

Department of Oncology, The Second Affiliated Hospital, Medical School of Xi'an Jiaotong University, Xi'an, 710004, China.

Department of Oncology, The Second Affiliated Hospital, Medical School of Xi'an Jiaotong University, Xi'an, 710004, China.

出版信息

Biomed Pharmacother. 2018 Feb;98:687-693. doi: 10.1016/j.biopha.2017.12.065. Epub 2018 Jan 4.

Abstract

In this study, the suppressive effect of sinomenine on the activation of SHh and the progression of breast cancer metastasis in vitro and in vivo was investigated. MDA-MB-231 breast cancer cells were treated with sinomenine and/or cyclopamine a proven SHh inhibitor. Sinomenine and cyclopamine both suppressed cell proliferation and migration, but sinomenine had a stronger suppressive effect in MDA-MB-231. In addition, sinomenine could suppress the activation of NF-κB and SHh signaling pathways, but cyclopamine could not suppress the activation of NF-κB. Subsequently, a mouse breast cancer-lung metastasis model was established. Our data on tissue examination and gene detection showed that SHh signaling was markedly activated in the metastatic model mice. The progression of lung metastasis was suppressed when mice were fed sinomenine and/or cyclopamine, while sinomenine had a stronger suppressive effect than cyclopamine in the model mice. In conclusion, sinomenine has a better effect than cyclopamine on the inhibition of breast cancer metastasis to lung in vivo and vitro, and inhibits NF-κB activation and NF-κB-mediated activation of SHh signaling pathway.

摘要

在这项研究中,研究了青藤碱对 SHh 激活和乳腺癌转移的体外和体内进展的抑制作用。用青藤碱和/或环巴胺(一种已证实的 SHh 抑制剂)处理 MDA-MB-231 乳腺癌细胞。青藤碱和环巴胺均可抑制细胞增殖和迁移,但青藤碱对 MDA-MB-231 的抑制作用更强。此外,青藤碱可抑制 NF-κB 和 SHh 信号通路的激活,但环巴胺不能抑制 NF-κB 的激活。随后,建立了小鼠乳腺癌肺转移模型。我们的组织检查和基因检测数据表明,转移模型小鼠中 SHh 信号明显激活。当用青藤碱和/或环巴胺喂养小鼠时,肺转移的进展受到抑制,而在模型小鼠中,青藤碱的抑制作用强于环巴胺。总之,青藤碱对体内和体外抑制乳腺癌向肺转移的效果优于环巴胺,可抑制 NF-κB 激活和 NF-κB 介导的 SHh 信号通路激活。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验