Anticancer and Immunomodulatory Activities of a Novel Water-Soluble Derivative of Ellipticine

被引:11
作者
de Oliveira, Regiane Costa [1 ]
Pontes, Gemilson Soares [1 ,2 ]
Kostyuk, Aleksandr [3 ]
Coutinho Camargo, Gabriel B. [1 ]
Dhyani, Anamika [2 ]
Shvydenko, Tetiana [3 ,4 ]
Shvydenko, Kostiantyn [3 ,4 ]
Grafov, Andriy [5 ]
机构
[1] Univ Estado Amazonas, Programa Posgrad Hematol, Av Djalma Batista 3578, Manaus, Amazonas, Brazil
[2] Inst Nacl de Pesquisas da Amazonia, Av Andre Araujo 2-936, Manaus, Amazonas, Brazil
[3] Natl Acad Sci Ukraine, Inst Organ Chem, Murmanska Str 5, UA-02660 Kiev, Ukraine
[4] JSC Farmak, Kyrylivska Str 63, UA-04080 Kiev, Ukraine
[5] Univ Helsinki, Dept Chem, Helsinki 00014, Finland
来源
MOLECULES | 2020年 / 25卷 / 09期
基金
欧盟地平线“2020”;
关键词
ellipticine; 9-bromoellipticine; sodium; 9-bromo-5; 11-dimethyl-6H-pyrido[4; 3-b]carbazole-7-sulfonate; immunomodulation; antitumor molecule; CELL-CYCLE; DRUG ELLIPTICINE; CANCER; IL-6; DNA; CYTOTOXICITY; PHASE;
D O I
10.3390/molecules25092130
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
Cancer still remains a major public health concern around the world and the search for new potential antitumor molecules is essential for fighting the disease. This study evaluated the anticancer and immunomodulatory potential of the newly synthetized ellipticine derivate: sodium bromo-5,11-dimethyl-6H-pyrido[4,3-b]carbazole-7-sulfonate (Br-Ell-SO3Na). It was prepared by the chlorosulfonation of 9-bromoellipticine. The ellipticine-7-sulfonic acid itself is not soluble, but its saponification with sodium hydroxide afforded a water-soluble sodium salt. The cytotoxicity of Br-Ell-SO3Na was tested against cancerous (K562 cell line) and non-cancerous cells (Vero cell line and human peripheral blood mononuclear cells (PBMC)) using a Methylthiazoletetrazolium (MTT) assay. Cell cycle arrest was assessed by flow cytometry and the immunomodulatory activity was analyzed through an enzyme-linked immunosorbent assay (ELISA)(.) The results showed that the Br-Ell-SO3Na molecule has specific anticancer activity (IC50 = 35 mu M) against the K562 cell line, once no cytotoxicity effect was verified against non-cancerous cells. Cell cycle analysis demonstrated that K562 cells treated with Br-Ell-SO3Na were arrested in the phase S. Moreover, the production of IL-6 increased and the expression of IL-8 was inhibited in the human PBMC treated with Br-Ell-SO3Na. The results demonstrated that Br-Ell-SO3Na is a promising anticancer molecule attested by its noteworthy activity against the K562 tumor cell line and immunomodulatory activity in human PBMC cells.
引用
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页数:12
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