Valadez-Vega Carmen, Morales-González José A, Sumaya-Martínez María Teresa, Delgado-Olivares Luis, Cruz-Castañeda Areli, Bautista Mirandeli, Sánchez-Gutiérrez Manuel, Zuñiga-Pérez Clara
Instituto de Ciencias de la Salud. Universidad Autónoma del Estado de Hidalgo. Ex Hacienda la Concepción s/n. Carr. Pachuca-Tilcuautla C.P. 42060 Tilcuautla, Hidalgo, Mexico.
Laboratorio Medicina de Conservación, Escuela Superior de Medicina, Instituto Politécnico Nacional, Plan de San Luis y Díaz Mirón s/n, Unidad Casco de Santo Tomas, México D.F. 11340, Mexico.
Molecules. 2014 Jul 7;19(7):9610-27. doi: 10.3390/molecules19079610.
For many years, several studies have been employing lectin from vegetables in order to prove its toxic effect on various cell lines. In this work, we analyzed the cytotoxic, antiproliferative, and post-incubatory effect of pure tepary bean lectins on four lines of malignant cells: C33-A; MCF-7; SKNSH, and SW480. The tests were carried out employing MTT and 3[H]-thymidine assays. The results showed that after 24 h of lectin exposure, the cells lines showed a dose-dependent cytotoxic effect, the effect being higher on MCF-7, while C33-A showed the highest resistance. Cell proliferation studies showed that the toxic effect induced by lectins is higher even when lectins are removed, and in fact, the inhibition of proliferation continues after 48 h. Due to the use of two techniques to analyze the cytotoxic and antiproliferative effect, differences were observed in the results, which can be explained by the fact that one technique is based on metabolic reactions, while the other is based on the 3[H]-thymidine incorporated in DNA by cells under division. These results allow concluding that lectins exert a cytotoxic effect after 24 h of exposure, exhibiting a dose-dependent effect. In some cases, the cytotoxic effect is higher even when the lectins are eliminated, however, in other cases, the cells showed a proliferative effect.
多年来,多项研究一直在使用来自蔬菜的凝集素,以证明其对各种细胞系的毒性作用。在这项工作中,我们分析了纯 tepary 豆凝集素对四种恶性细胞系(C33 - A、MCF - 7、SKNSH 和 SW480)的细胞毒性、抗增殖和孵育后效应。测试采用 MTT 和 3[H] - 胸腺嘧啶核苷测定法进行。结果表明,凝集素暴露 24 小时后,细胞系呈现剂量依赖性细胞毒性作用,对 MCF - 7 的作用更强,而 C33 - A 表现出最高的抗性。细胞增殖研究表明,即使去除凝集素,其诱导的毒性作用仍然较高,事实上,48 小时后增殖抑制仍在继续。由于使用了两种技术来分析细胞毒性和抗增殖作用,结果中观察到了差异,这可以解释为一种技术基于代谢反应,而另一种基于细胞在分裂时掺入 DNA 中的 3[H] - 胸腺嘧啶核苷。这些结果表明,凝集素暴露 24 小时后发挥细胞毒性作用,呈现剂量依赖性效应。在某些情况下,即使去除凝集素,细胞毒性作用仍然较高,然而,在其他情况下,细胞表现出增殖效应。