NVP-BEZ235/Chlorin-e6 co-loaded nanoparticles ablate breast cancer by biochemical and pnotodynamic synergistic effects

被引:6
作者
Eltahan, Ahmed Shaker [1 ,2 ]
Liu, Lu [1 ,2 ,4 ]
Okeke, Chukwunweike Ikechukwu [1 ,2 ]
Huang, Min [5 ]
Han, Lu [5 ]
Chen, Jing [1 ]
Xue, Xue [3 ]
Bottini, Massimo [1 ,4 ]
Guo, Weisheng [1 ]
Liang, Xing-Jie [1 ,2 ]
机构
[1] Natl Ctr Nanosci & Technol China, CAS Ctr Excellence Nanosci, CAS Key Lab Biomed Effects Nanomat & Nanosafety, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Nankai Univ, Coll Pharm, State Key Lab Med Chem Biol, Tianjin 300350, Peoples R China
[4] Univ Roma Tor Vergata, Dept Expt Med & Surg, I-00133 Rome, Italy
[5] Beijing Inst Graph Commun, Beijing Engn Res Ctr Printed Elect, Beijing 102600, Peoples R China
基金
中国国家自然科学基金;
关键词
nanomedicine; triple-negative breast cancer; NVP-BEZ235; photodynamic therapy; synergistic therapy; PI3K/MTOR INHIBITOR NVP-BEZ235; PHOTODYNAMIC THERAPY; DNA-DAMAGE; SUBTYPES; CHALLENGES; PATHWAY; OPPORTUNITIES; PROGNOSIS; PROMOTES; STRESS;
D O I
10.1007/s12274-018-2074-0
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Seeking profitable therapies for triple-negative breast cancer (TNBC) has attracted intense research interest. However, an efficient cure for TNBC remains an unresolved challenge in oncology. Herein, for the first time, we describe the use of polymeric nanoparticles loaded with NVP-BEZ235 and Chlorin-e6, denoted as NVP/Ce6@NPs, to overcome the adaptive treatment tolerance of TNBC by taking advantage of the synergistic effect between biochemical and photodynamic therapies. Upon laser irradiation, the NVP/Ce6@NPs generated reactive oxygen species (ROS) and efficiently induced the apoptosis of tumor cells through DNA damage. Furthermore, the released NVP-BEZ235 could prevent Chk1 phosphorylation-induced DNA damage repair, thus enhancing the sensitivity of tumor cells to ROS. Animal studies on mice bearing an MDA-MB-231 tumor validated that the NVP/Ce6@NPs had a greater therapeutic efficacy compared to that of monotherapies, with an inhibition ratio of 89.3%. Western blotting and cell viability analyses confirmed the inhibition of both MDA-MB-231 cell proliferation and Chk1 phosphorylation by NVP/Ce6@NPs. These findings provide a rational understanding of the synergistic effect of the biochemical/photodynamic therapy and pave the way for the development of efficient therapeutic approaches to fight against TNBC.
引用
收藏
页码:4846 / 4858
页数:13
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