Synthesis and biological evaluation of novel peptides based on antimicrobial peptides as potential agents with antitumor and multidrug resistance-reversing activities

被引:17
作者
Zhang, Bo [1 ]
Shi, Wei [1 ]
Li, Jieming [1 ]
Liao, Chen [1 ]
Yang, Limei [1 ]
Huang, Wenlong [1 ,2 ]
Qian, Hai [1 ,2 ]
机构
[1] China Pharmaceut Univ, Ctr Drug Discovery, State Key Lab Nat Med, Nanjing, Jiangsu, Peoples R China
[2] China Pharmaceut Univ, Jiangsu Key Lab Drug Discovery Metab Dis, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
anticancer; antimicrobial peptides; helix; membrane disruption; multidrug resistance-reversing effects; PHOSPHOLIPIDS; ANTICANCER; MECHANISMS; APOPTOSIS; MEMBRANES; DESIGN; CHARGE;
D O I
10.1111/cbdd.13023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tumor chemotherapy, which plays an important role in the clinical treatment of metastatic cancer, is limited by low selectivity and drug resistance in clinical application. In our study, we selected antimicrobial peptide BP100 as a lead peptide, designed, and synthesized a series of novel antineoplastic peptides through solid-phase synthesis. Among them, B4 and B8 showed excellent anticancer activity. As revealed by further investigations, these peptides could disrupt the cell membrane, trigger the cytochrome C release into cytoplasm, and ultimately lead to apoptosis. In addition, they also showed multidrug resistance-reversing effects by performing effective antitumor activity against multidrug-resistant cells. As a result, these peptides may possibly be regarded as a promising candidate for cancer treatment.
引用
收藏
页码:972 / 980
页数:9
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