PEGylated Hyaluronic Acid-Modified Liposomal Delivery System with Anti-γ-Glutamylcyclotransferase siRNA for Drug-Resistant MCF-7 Breast Cancer Therapy

2015 ◽  
Vol 104 (2) ◽  
pp. 476-484 ◽  
Author(s):  
Rui Ran ◽  
Yayuan Liu ◽  
Huile Gao ◽  
Qifang Kuang ◽  
Qianyu Zhang ◽  
...  
2014 ◽  
Vol 6 (9) ◽  
pp. 6469-6480 ◽  
Author(s):  
Raju Vivek ◽  
Ramar Thangam ◽  
Varukattu NipunBabu ◽  
Chandrababu Rejeeth ◽  
Srinivasan Sivasubramanian ◽  
...  

2018 ◽  
Vol 51 (5) ◽  
pp. e12488 ◽  
Author(s):  
Tingting Kong ◽  
Liying Hao ◽  
Yuanyuan Wei ◽  
Xiaoxiao Cai ◽  
Bofeng Zhu

Drug Delivery ◽  
2015 ◽  
Vol 23 (4) ◽  
pp. 1364-1368 ◽  
Author(s):  
Qian Liu ◽  
Jia Li ◽  
Gaobin Pu ◽  
Fang Zhang ◽  
Hongyan Liu ◽  
...  

2018 ◽  
Vol 6 (19) ◽  
pp. 3163-3180 ◽  
Author(s):  
Caifeng Deng ◽  
Xiaohong Xu ◽  
Drunp Tashi ◽  
Yongmei Wu ◽  
Bingyin Su ◽  
...  

The safe and efficient targeted delivery of chemotherapeutic drugs has remained a challenge in metastatic breast cancer therapy.


2021 ◽  
Vol 133 ◽  
pp. 111053
Author(s):  
Dorota Bartusik-Aebisher ◽  
Grzegorz Chrzanowski ◽  
Zuzanna Bober ◽  
David Aebisher

Drug Delivery ◽  
2021 ◽  
Vol 29 (1) ◽  
pp. 1-9
Author(s):  
Yun-Chang Zhang ◽  
Pei-Yu Zeng ◽  
Zhi-Qiang Ma ◽  
Zi-Yue Xu ◽  
Ze-Kun Wang ◽  
...  

Biomolecules ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1623
Author(s):  
Diana Duarte ◽  
Nuno Vale

Chemotherapy plays a key role in breast cancer therapy, but drug resistance and unwanted side effects make the treatment less effective. We propose a new combination model that combines antineoplastic drugs and antimalarials for breast cancer therapy. Cytotoxic effects of two antineoplastic agents alone and in combination with several antimalarials on MCF-7 tumor cell line was evaluated. Different concentrations in a fixed ratio were added to the cultured cells and incubated for 48 h. Cell viability was evaluated using MTT and SRB assays. Synergism was evaluated using the Chou-Talalay method. The results indicate doxorubicin (DOX) and paclitaxel (PTX) alone at concentrations of their IC50 and higher are cell growth inhibitors. Mefloquine, artesunate, and chloroquine at concentrations of their IC50 demonstrate anti-cancer activity. In combination, almost all antimalarials demonstrate higher ability than DOX and PTX alone to decrease cell viability at concentrations of IC50 and lower than their IC50. The combination of chloroquine, artesunate and mefloquine with DOX and PTX was synergic (CI < 1). The combination of DOX and mefloquine after 48 h incubation demonstrated the highest cytotoxicity against MCF-7 cells, and the combination of DOX and artesunate was the most synergic. These results suggest antimalarials could act synergistically with DOX/PTX for breast cancer therapy.


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