Multifunctional targeting daunorubicin plus quinacrine liposomes, modified by wheat germ agglutinin and tamoxifen, for treating brain glioma and glioma stem cells

被引:43
作者
Li, Xue-Tao [1 ,2 ]
Ju, Rui-Jun [1 ]
Li, Xiu-Ying [1 ]
Zeng, Fan [1 ]
Shi, Ji-Feng [1 ]
Liu, Lei [1 ]
Zhang, Cheng-Xiang [1 ]
Sun, Meng-Ge [1 ]
Lou, Jin-Ning [3 ]
Lu, Wan-Liang [1 ]
机构
[1] Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing 100871, Peoples R China
[2] Liaoning Univ Tradit Chinese Med, Sch Pharm, Dalian, Peoples R China
[3] Chia Japan Friendship Hosp, Minist Hlth, Inst Clin Med Sci, Beijing, Peoples R China
基金
美国国家科学基金会; 北京市自然科学基金;
关键词
multifunctional targeting liposomes; wheat germ agglutinin; daunorubicin; tamoxifen; brain glioma stem cells; BREAST-CANCER; DRUG TRANSPORT; IN-VITRO; BARRIER; APOPTOSIS; DELIVERY; THERAPY; CHEMOTHERAPY; DOXORUBICIN; PACLITAXEL;
D O I
10.18632/oncotarget.2267
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Most anticancer drugs are not able to cross the blood-brain barrier (BBB) effectively while surgery and radiation therapy cannot eradicate brain glioma cells and glioma stem cells (GSCs), hence resulting in poor prognosis with high recurrence rates. In the present study, a kind of multifunctional targeting daunorubicin plus quinacrine liposomes was developed for treating brain glioma and GSCs. Evaluations were performed on in-vitro BBB model, murine glioma cells, GSCs, and GSCs bearing mice. Results showed that the multifunctional targeting daunorubicin plus quinacrine liposomes exhibited evident capabilities in crossing the BBB, in killing glioma cells and GSCs and in diminishing brain glioma in mice. Action mechanism studies indicated that the enhanced efficacy of the multifunctional targeting drugs-loaded liposomes could be due to the following aspects: evading the rapid elimination from blood circulation; crossing the BBB effectively; improving drug uptake by glioma cells and GSCs; down-regulating the overexpressed ABC transporters; inducing apoptosis of GSCs via up-regulating apoptotic receptor/ligand (Fas/Fasl), activating apoptotic enzymes (caspases 8, 9 and 3), activating pro-apoptotic proteins (Bax and Bok), activating tumor suppressor protein (P53) and suppressing anti-apoptotic proteins (Bcl-2 and Mcl-1). In conclusion, the multifunctional targeting daunorubicin plus quinacrine liposomes could be used as a potential therapy for treating brain glioma and GSCs.
引用
收藏
页码:6497 / 6511
页数:15
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