Smart glypican-3-targeting peptide-chlorin e6 conjugates for targeted photodynamic therapy of hepatocellular carcinoma

被引:8
|
作者
Fang, Yuxin [1 ]
Ma, Haoqian [1 ]
Zhang, Xianghua [3 ]
Zhang, Peifeng [1 ,4 ]
Li, Yu [1 ]
He, Shipeng [2 ]
Sheng, Chunquan [1 ]
Dong, Guoqiang [1 ]
机构
[1] Naval Med Univ, Second Mil Med Univ, Ctr Basic Res & Innovat Med & Pharm MOE, Sch Pharm, 325 Guohe Rd, Shanghai 200433, Peoples R China
[2] Shanghai Univ, Inst Translat Med, 99 Shangda Rd, Shanghai 200444, Peoples R China
[3] Second Mil Med Univ, Eastern Hepatobiliary Surg Hosp, Dept Hepat Surg, Shanghai 200003, Peoples R China
[4] Changzhou Univ, Natl & Local Joint Engn Res Ctr High Efficiency Re, Sch Pharm, Changzhou 213164, Peoples R China
基金
中国国家自然科学基金;
关键词
Glypican-3; Targeted photodynamic therapy; Peptide-drug conjugates; Chlorin e6; Hepatocellular carcinoma; Cancer treatment; POTENT PHOTOSENSITIZERS; BACTERIOPURPURINIMIDES;
D O I
10.1016/j.ejmech.2023.116047
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Hepatocellular carcinoma (HCC) is a highly aggressive and lethal malignancy with poor prognosis, necessitating the urgent development of effective treatments. Targeted photodynamic therapy (PDT) offers a promising way to selectively eradicate tumor cells without affecting normal cells. Inspired by promising features of peptide-drug conjugates (PDCs) in targeted cancer therapy, herein a novel glypican-3 (GPC3)-targeting PDC-PDT strategy was developed for the precise PDT treatment of HCC. The GPC3-targeting photosensitizer conjugates were developed by attaching GPC3-targeting peptides to chlorin e6. Conjugate 8b demonstrated the ability to penetrate HCC cells via GPC3-mediated entry process, exhibiting remarkable tumor-targeting capacity, superior antitumor efficacy, and minimal toxicity towards normal cells. Notably, conjugate 8b achieved complete tumor elimination upon light illumination in a HepG2 xenograft model without harm to normal tissues. Overall, this innovative GPC3-targeting conjugation strategy demonstrates considerable promise for clinical applications for the treatment of HCC.
引用
收藏
页数:10
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