An online coupled breast cancer cell membrane chromatography with HPLC/MS for screening active compounds from Fructus evodiae

2013 ◽  
Vol 5 (20) ◽  
pp. 5767 ◽  
Author(s):  
Xilong Yuan ◽  
Bing Zhang ◽  
Yunan Wang ◽  
Jing Ma ◽  
Xiaofang Hou

2005 ◽  
Vol 11 (12) ◽  
pp. 4357-4364 ◽  
Author(s):  
Huayi Huang ◽  
Jeff Groth ◽  
Khalid Sossey-Alaoui ◽  
Lesleyann Hawthorn ◽  
Stephanie Beall ◽  
...  


2017 ◽  
Vol 18 (4) ◽  
pp. 375-380 ◽  
Author(s):  
Shadab Shahriari ◽  
Somayeh Rezaeifard ◽  
Hamid Reza Moghimi ◽  
Mohammad Reza Khorramizadeh ◽  
Zahra Faghih


2021 ◽  
Author(s):  
Yingshu Guo ◽  
Xiaofei Zheng ◽  
Tingting Gai ◽  
Zhiyong Wei ◽  
Shu-Sheng Zhang

Here, the co-membrane system of MCF-7 breast cancer cell membrane (MM) and Escherichia coli membrane (EM)-coated Fe3O4/MnO2 multifunctional composite nanoparticles loaded with DOX (Fe3O4/MnO2/MM/EM/D) was used for targeting drug delivery...



2010 ◽  
Vol 17 (2) ◽  
pp. 431-443 ◽  
Author(s):  
Xiao-Dong Fu ◽  
Lorenzo Goglia ◽  
Angel Matias Sanchez ◽  
Marina Flamini ◽  
Maria S Giretti ◽  
...  

While progesterone plays multiple roles in the process of breast development and differentiation, its role in breast cancer is less understood. We have shown previously that progestins stimulate breast cancer cell migration and invasion because of the activation of rapid signaling cascades leading to modifications in the actin cytoskeleton and cell membrane that are required for cell movement. In this study, we have investigated the effects of progesterone on the formation of focal adhesion (FA) complexes, which provide anchoring sites for cell attachment to the extracellular matrix during cell movement and invasion. In T47-D breast cancer cells, progesterone rapidly enhances FA kinase (FAK) phosphorylation at Tyr397 in a time- and concentration-dependent manner. As a result, exposure to progesterone leads to increased formation of FA complexes within specialized cell membrane protrusions. The cascade of events required for this phenomenon involves progesterone receptor interaction with the tyrosine kinase c-Src, which activates the phosphatidylinositol-3-kinase/Akt pathway and the small GTPase RhoA/Rho-associated kinase complex. In the presence of progesterone, T47-D breast cancer cells display enhanced horizontal migration and invasion of three-dimensional matrices, which is reversed by small interfering RNAs abrogating FAK. In conclusion, progesterone promotes breast cancer cell movement and invasion by facilitating the formation of FA complexes via the rapid regulation of FAK. These results provide novel mechanistic views on the effects of progesterone on breast cancer progression, and may in the future be helpful to develop new strategies for the treatment of endocrine-sensitive breast cancers.



2016 ◽  
Vol Volume 11 ◽  
pp. 5149-5161 ◽  
Author(s):  
Carlos Lara Cruz ◽  
Javier Jimenez Salazar ◽  
Eva Ramon Gallegos ◽  
Pablo Damian Matsumura ◽  
Nikola Batina


2004 ◽  
Vol 21 (12) ◽  
pp. 2543-2546 ◽  
Author(s):  
Guo Hong-Lian ◽  
Liu Chun-Xiang ◽  
Duan Jian-Fa ◽  
Jiang Yu-Qiang ◽  
Han Xue-Hai ◽  
...  




Sign in / Sign up

Export Citation Format

Share Document