Design, synthesis and biological evaluation of novel peptides as potential agents with anti-tumor and multidrug resistance-reversing activities

被引:6
作者
Zhang, Bo [1 ]
Shi, Wei [1 ]
Li, Jieming [1 ]
Liao, Chen [1 ]
Li, Mingxue [1 ]
Huang, Wenlong [1 ,2 ]
Qian, Hai [1 ,2 ]
机构
[1] China Pharmaceut Univ, State Key Lab Nat Med, Ctr Drug Discovery, 24 Tongjiaxiang, Nanjing 210009, Jiangsu, Peoples R China
[2] China Pharmaceut Univ, Jiangsu Key Lab Drug Discovery Metab Dis, 24 Tongjiaxiang, Nanjing 210009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Anti-cancer; Multidrug resistance-reversing effects; Membrane-disruption; Antimicrobial peptides; MEMBRANES; PHOSPHOLIPIDS; MITOCHONDRIA; ANTICANCER; MECHANISMS; APOPTOSIS; CHARGE; CELLS;
D O I
10.1007/s00726-017-2434-1
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 is an important mean in the clinical treatment of metastatic cancer,but low selectivity and drug resistance restrict its clinical application. BP100 is a multifunctional membrane-active peptide with high antimicrobial activity. We selected BP100 as a lead peptide, designed and synthesized a series of BP100 analogs through solid-phase synthesis. Amongst them, peptides with the Tyr10 residue substituted by leucine and histidine showed the highest anti-cancer activity. Further experiments revealed that BP100 and its analogs could disrupt the cell membrane and trigger the cytochrome C release into cytoplasm, which ultimately resulted in apoptosis. Meanwhile, BP100 and its analogs also exhibited effective anti-tumor activity against multidrug-resistant cells, showing multidrug resistance-reversing effects. In conclusion, these peptides might be promising candidates for cancer therapy.
引用
收藏
页码:1355 / 1364
页数:10
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