A fish antimicrobial peptide, tilapia hepcidin TH2-3, shows potent antitumor activity against human fibrosarcoma cells

被引:99
|
作者
Chen, Jyh-Yih [1 ,2 ]
Lin, Wei-Ju [1 ]
Lin, Tai-Lang [3 ]
机构
[1] Acad Sinica, Inst Cellular & Organism Biol, Marine Res Stn, Jiaushi 262, Ilan, Taiwan
[2] Natl Taiwan Ocean Univ, Inst Biosci & Biotechnol, Chilung 202, Taiwan
[3] Acad Sinica, Inst Cellular & Organism Biol, Taipei 110, Taiwan
关键词
Hepcidin; Tumor cell inhibition; Lytic peptide; IRON-METABOLISM; KEY REGULATOR; EXPRESSION;
D O I
10.1016/j.peptides.2009.06.009
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
As part of a continuing search for potential anticancer drug candidates from antimicrobial peptides of marine organisms, tilapia (Oreochromis mossambicus) hepcidin TH2-3 was evaluated in several tumor cell lines. The results indicated that TH2-3, a synthetic 20-mer antimicrobial peptide, specifically inhibited human fibrosarcoma cell (HT1080 cell line) proliferation and migration. The way in which TH23 inhibited HT1080 cell growth was then studied. TH2-3 inhibited HT1080 cell growth in a concentration-dependent manner according to an MTT analysis. which was confirmed by a soft-agar assay and AO/EtBr staining. Scanning electron microscopy revealed that TH2-3 caused lethal membrane disruption in HT1080 cancer cells, and a wound healing assay supported that TH2-3 decreased the migration of HT1080 cells. In addition, c-Jun mRNA expression was downregulated after treatment with TH2-3 for 48-96 h compared to the untreated group. These findings suggest a mechanism of cytotoxic action of TH2-3 and indicate that TH2-3 may be a promising chemotherapeutic agent against human fibrosarcoma cells. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:1636 / 1642
页数:7
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