Modularly designed peptide-based nanomedicine inhibits angiogenesis to enhance chemotherapy for post-surgical recurrence of esophageal squamous cell carcinomas

被引:5
作者
Qi, Yingqiu [1 ]
Shen, Jinxiu [1 ]
Liu, Chen [1 ,2 ]
Du, Anni [1 ,2 ]
Chen, Mengdie [1 ]
Meng, Xiaocao [1 ,2 ]
Wang, Hui [1 ]
Zhang, Saiyang [1 ]
Zhang, Lirong [1 ,3 ]
Li, Zhongjun [4 ]
Li, Yike [4 ]
Yue, Yale [1 ]
Min, Huan [2 ]
机构
[1] Zhengzhou Univ, Dept Pharmacol, Sch Basic Med Sci, Zhengzhou 450001, Peoples R China
[2] Zhengzhou Univ, Henan Inst Adv Technol, Zhengzhou 450001, Peoples R China
[3] State Key Lab Esophageal Canc Prevent & Treatment, Zhengzhou 450001, Peoples R China
[4] Zhengzhou Univ, Coll Chem, Inst Green Catalysis, Zhengzhou 450001, Henan, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
esophageal squamous cell carcinomas; peptide-based nanomedicine; anti-angiogenesis; oridonin; chemotherapy; CANCER; ORIDONIN; SURGERY; VEGF; METASTASIS; RESECTION; BLOCKADE; GROWTH; RISK;
D O I
10.1007/s12274-023-5396-5
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
Traditional surgical treatment is difficult to thoroughly remove esophageal squamous cell carcinomas (ESCC), and postoperative recurrence caused by residual tumor cells is a critical factor in the poor prognosis. Since surgical resection promotes the local angiogenesis at the tumor site, further exacerbating the proliferation and invasion of residual tumor cells, it is urgent to inhibit angiogenesis after surgery. Here, a functional peptide-based nanomedicine was obtained from peptide-drug conjugates, which are composed of a hydrophilic targeting motif (vascular endothelial growth factor family and their receptors (VEGFR) targeting peptide for anti-angiogenesis), and an ester-linked hydrophobic oridonin (ORI). The nanomedicine exhibits esterase-catalyzed disassembly and drug release, and significantly enhanced the anti-tumor efficacy of chemotherapeutics in a postoperative tumor recurrence model through synergistic anti-angiogenic strategies. This study provides an integrated solution for anti-angiogenesis-augmented chemotherapy and demonstrates the encouraging potential for postoperative treatment.
引用
收藏
页码:7347 / 7354
页数:8
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