A novel matrix metalloproteinase-2 inhibitor triazolylmethyl aziridine reduces melanoma cell invasion, angiogenesis and targets ERK1/2 phosphorylation

被引:11
作者
Romanchikova, Nadezhda [1 ]
Trapencieris, Peteris [1 ]
Zemitis, Janis [2 ]
Turks, Maris [2 ]
机构
[1] Latvian Inst Organ Synth, LV-1006 Riga, Latvia
[2] Riga Tech Univ, Fac Mat Sci & Appl Chem, Riga, Latvia
关键词
Angiogenesis; aziridine-triazole conjugate; drug discovery; invasion; matrix metalloproteinase inhibitor; melanoma; ENDOTHELIAL GROWTH-FACTOR; ACTIVATED PROTEIN-KINASE; IN-VITRO; TUMOR-GROWTH; ENANTIOSPECIFIC APPROACH; LUNG METASTASIS; CANCER; EXPRESSION; MMP-2; INACTIVATION;
D O I
10.3109/14756366.2013.855207
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
A novel matrix metalloproteinase-2 (MMP-2) inhibitor JaZ-30, which belongs to the class of C(2)-monosubstituted aziridine - aryl-1,2,3-triazole conjugates, was developed. MTT and crystal violet assays were used to determine cytotoxicity-IC(50) values of compound JaZ-30 on melanoma cell line B16 4A5. Our study proves the anti-cancer properties of JaZ-30 with a wide spectrum of activities. JaZ-30 was revealed as selective inhibitor of matrix metalloproteinase-2. JaZ-30-mediated decrease of Vascular Endothelial Growth Factor (VEGF) secretion results in inhibition of angiogenesis, performed with the human umbilical vein endothelial cell line (HUVEC-2) on Matrigel. A novel inhibitor decreases invasive properties of melanoma cells measured in Matrigel chambers assay. JaZ-30 downregulates phosphorylation of the extracellular signal-regulated kinases 1 and 2 (ERK1/2) in melanoma cells stimulated by phorbol-12-myristate-13-acetate (PMA). Our findings propose a novel MMP-2 inhibitor JaZ-30 as an attractive potential agent for melanoma treatment.
引用
收藏
页码:765 / 772
页数:8
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