Targeted Chinese Medicine Delivery by A New Family of Biodegradable Pseudo-Protein Nanoparticles for Treating Triple-Negative Breast Cancer: In Vitro and In Vivo Study

被引:12
作者
Kwan, Hiu Yee [1 ]
Xu, Qinghua [2 ]
Gong, Ruihong [1 ]
Bian, Zhaoxiang [1 ]
Chu, Chih-Chang [2 ]
机构
[1] Hong Kong Baptist Univ, Sch Chinese Med, Hong Kong, Peoples R China
[2] Cornell Univ, Dept Fiber Sci & Apparel Design, Biomed Engn Field & Fiber Sci Program, Ithaca, NY 14850 USA
关键词
triple-negative breast cancer; gambogic acid; nanoparticle; poly(ester amide)s; apoptosis; tumor-associated macrophage; GAMBOGIC ACID; SIALIC-ACID; MITOCHONDRIAL; EXPRESSION; APOPTOSIS; TISSUES;
D O I
10.3389/fonc.2020.600298
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Triple negative breast cancer (TNBC) has the worst overall survival among all breast cancer subtypes; 80% of TNBC harbors TP53 mutation. Gambogic acid (GA) is an herbal compound isolated from the dry brownish gamboge resin of Garcinia hanburyi. A new family of biodegradable polymer, the folate (FA)-conjugated arginine-based poly(ester urea urethane)s nanoparticles (FA-Arg-PEUU NP), was developed as nano-carrier for GA. Its anti-TNBC effects and the underlying mechanism of action were examined. The average diameters of FA-Arg-PEUU NP and GA-loaded FA-Arg-PEUU NP (NP-GA) in water are around 165 and 220nm, respectively. Rhodamine-tagged FA-Arg-PEUU NP shows that the conjugation of FA onto Arg-PEUU NPs facilitates the internalization of FA-Arg-PEUU-NP into TNBC. Compared to free-GA at the same GA concentrations, NP-GA exhibits higher cytotoxicity in both TP53-mutated and non-TP53 expressed TNBC cells by increasing intrinsic and extrinsic apoptosis. In HCC1806-bearing xenograft mouse model, the targeted delivery of GA by the FA-Arg-PEUU-NP nano-carriers to the tumor sites results in a more potent anti-TNBC effect and lower toxicity towards normal tissues and organs when compared to free GA. Furthermore, NP-GA also reduces the tumor-associated macrophage (TAM) M1/M2 ratio, suggesting that the use of Arg-based nanoparticles as carriers for GA not only makes the surface of the nanoparticles positively charged, but also confers on to the nanoparticles an ability to modulate TAM polarization. Our data clearly demonstrate that NP-GA exhibits potent anti-TNBC effects with reduced off-target toxicity, which represents novel alternative targeted therapeutics for TNBC treatment.
引用
收藏
页数:18
相关论文
共 62 条
[11]   Synthesis and characterization of novel biodegradable unsaturated poly(ester amide)/poly(ethylene glycol) diacrylate hydrogels [J].
Guo, K ;
Chu, CC .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2005, 43 (17) :3932-3944
[12]   Biodegradable amino acid-based poly(ester amine) with tunable immunomodulating properties and their in vitro and in vivo wound healing studies in diabetic rats' wounds [J].
He, Mingyu ;
Sun, Luyao ;
Fu, Xiaoling ;
McDonough, Sean P. ;
Chu, Chih-Chang .
ACTA BIOMATERIALIA, 2019, 84 :114-132
[13]   Folate-decorated arginine-based poly(ester urea urethane) nanoparticles as carriers for gambogic acid and effect on cancer cells [J].
He, Mingyu ;
Ro, Lillian ;
Liu, Jing ;
Chu, Chih-Chang .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2017, 105 (02) :475-490
[14]  
Holmberg AR, 1999, CLIN CANCER RES, V5, p3056S
[15]   The use of neoadjuvant platinum-based chemotherapy in locally advanced breast cancer that is triple negative: retrospective analysis of 144 patients [J].
Hurley, Judith ;
Reis, Isildinha M. ;
Rodgers, Steven E. ;
Gomez-Fernandez, Carmen ;
Wright, Jean ;
Leone, Jose Pablo ;
Larrieu, Rene ;
Pegram, Mark D. .
BREAST CANCER RESEARCH AND TREATMENT, 2013, 138 (03) :783-794
[16]   A Novel Pseudo-Protein-Based Biodegradable Nanomicellar Platform for the Delivery of Anticancer Drugs [J].
Ji, Ying ;
Shan, Shuo ;
He, Mingyu ;
Chu, Chih-Chang .
SMALL, 2017, 13 (01)
[17]   Roles of IFN-γ in tumor progression and regression: a review [J].
Jorgovanovic, Dragica ;
Song, Mengjia ;
Wang, Liping ;
Zhang, Yi .
BIOMARKER RESEARCH, 2020, 8 (01)
[18]  
Katsarava R, 1999, J POLYM SCI POL CHEM, V37, P391, DOI 10.1002/(SICI)1099-0518(19990215)37:4<391::AID-POLA3>3.0.CO
[19]  
2-E
[20]  
KAWAI T, 1991, CANCER RES, V51, P1242