Lactoferrin-Modified Gambogic Acid Liposomes for Colorectal Cancer Treatment

被引:9
作者
Wang, Rong [1 ,2 ,5 ]
Qu, Jingkun [3 ]
Tang, Xueping [6 ]
Zhang, Jiaxin [2 ]
Ou, Ante [2 ]
Li, Qianqian [2 ,5 ]
Chen, Guihua [2 ,6 ]
Zheng, Caihong [1 ]
Muhitdinov, Bahtiyor [2 ,7 ]
Huang, Yongzhuo [2 ,3 ,4 ]
机构
[1] Zhejiang Univ, Womens Hosp, Dept Pharm, Sch Med, Hangzhou 310006, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China
[3] Nanjing Univ Chinese Med, Sch Chinese Mat Med, 138 Xianlin Ave, Nanjing 210023, Peoples R China
[4] Chinese Acad Sci, Zhongshan Inst Drug Discovery, Shanghai Inst Mat Med, Zhongshan 528437, Peoples R China
[5] Nanchang Univ, Coll Pharm, Nanchang 330006, Peoples R China
[6] Guangzhou Univ Chinese Med, Artemisinin Res Ctr, 12 Jichang Rd, Guangzhou 510450, Peoples R China
[7] Uzbek Acad Sci, Inst Bioorgan Chem, 83 M Ulughbek St, Tashkent 100125, Uzbekistan
关键词
Colorectal cancer; Gambogic acid; Lactoferrin; Liposome; Tumor drug delivery; TUMOR-ASSOCIATED MACROPHAGES; RECEPTOR-RELATED PROTEIN-1; PEGYLATED LIPOSOMES; TISSUE DISTRIBUTION; PANCREATIC-CANCER; PHARMACOKINETICS; EXPRESSION; EXCRETION; APOPTOSIS;
D O I
10.1021/acs.molpharmaceut.3c00052
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Colorectal cancer (CRC) therapy is a big challenge, andseekingan effective and safe drug is a pressing clinical need. Gambogic acidis a potent antineoplastic agent without the drawback of bone marrowsuppression. To improve its druggability (e.g., poor water solubilityand tumor delivery), a lactoferrin-modified gambogic acid liposomaldelivery system (LF-lipo) was developed to enhance the treatment efficacyof CRC. The LF-lipo can specifically bind LRP-1 expressed on colorectalcancer cells to enhance drug delivery to the tumor cells and yieldenhanced therapeutic efficacy. The LF-lipo promoted tumor cell apoptosisand autophagy, reduced reactive oxygen species (ROS) levels in tumorcells, and inhibited angiogenesis; moreover, it could also repolarizetumor-associated macrophages from the M2 to M1 phenotype and induceICD to activate T cells, exhibiting the capability of remodeling thetumor immune microenvironment. The liposomal formulation yielded anefficient and safe treatment outcome and has potential for clinicaltranslation.
引用
收藏
页码:3925 / 3936
页数:12
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