A Lactose-Binding Lectin from the Marine Sponge Cinachyrella Apion (Cal) Induces Cell Death in Human Cervical Adenocarcinoma Cells

被引:39
|
作者
Rabelo, Luciana [1 ]
Monteiro, Norberto [1 ]
Serquiz, Raphael [1 ]
Santos, Paula [1 ]
Oliveira, Ruth [1 ]
Oliveira, Adeliana [1 ]
Rocha, Hugo [1 ]
Morais, Ana Heloneida [2 ]
Uchoa, Adriana [3 ]
Santos, Elizeu [1 ]
机构
[1] Univ Fed Rio Grande do Norte, Dept Biochem, BR-59072970 Natal, RN, Brazil
[2] Univ Fed Rio Grande do Norte, Dept Nutr, BR-59072970 Natal, RN, Brazil
[3] Univ Fed Rio Grande do Norte, Dept Cellular Biol & Genet, BR-59072970 Natal, RN, Brazil
来源
MARINE DRUGS | 2012年 / 10卷 / 04期
关键词
HeLa; lectin; antitumor; marine sponge; Cinachyrella apion; ALBUM AGGLUTININ-I; NF-KAPPA-B; INDUCED APOPTOSIS; CYCLE ARREST; CLINICAL-APPLICATIONS; NATURAL COMPOUNDS; CANCER CELLS; INDUCTION; GROWTH; MECHANISMS;
D O I
10.3390/md10040727
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Cancer represents a set of more than 100 diseases, including malignant tumors from different locations. Strategies inducing differentiation have had limited success in the treatment of established cancers. Marine sponges are a biological reservoir of bioactive molecules, especially lectins. Several animal and plant lectins were purified with antitumor activity, mitogenic, anti-inflammatory and antiviral, but there are few reports in the literature describing the mechanism of action of lectins purified from marine sponges to induce apoptosis in human tumor cells. In this work, a lectin purified from the marine sponge Cinachyrella apion (CaL) was evaluated with respect to its hemolytic, cytotoxic and antiproliferative properties, besides the ability to induce cell death in tumor cells. The antiproliferative activity of CaL was tested against HeLa, PC3 and 3T3 cell lines, with highest growth inhibition for HeLa, reducing cell growth at a dose dependent manner (0.5-10 mu g/mL). Hemolytic activity and toxicity against peripheral blood cells were tested using the concentration of IC50 (10 mu g/mL) for both trials and twice the IC50 for analysis in flow cytometry, indicating that CaL is not toxic to these cells. To assess the
引用
收藏
页码:727 / 743
页数:17
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