Taborga Lautaro, Espinoza Luis, Moller Alejandra, Carrasco Héctor, Cuellar Mauricio, Villena Joan
Departamento de Química, Universidad Técnica Federico Santa María, Av. España 1680, Valparaíso, 2390123, Chile.
Centro Investigaciones Biomédicas (CIB), Facultad de Medicina, Universidad de Valparaíso, Hontaneda 2653, Valparaíso, 2341386, Chile.
Chem Biol Interact. 2016 Mar 5;247:22-9. doi: 10.1016/j.cbi.2016.01.016. Epub 2016 Jan 28.
Sixteen synthetic linear derivatives geranylphenols, were obtained from phloroglucinol and orcinol, and cytotoxic activity was evaluated in vitro against cancer cell lines (HT-29, PC-3, MDA-MB231, DU-145) and one non-tumor cell line, human dermal fibroblast (HDF). IC50 values were determined at concentrations of 0-100 μM of each compound for 72 h. Compounds 12, 13, 17, 21, 22 and 25, showed cytotoxic activity. To elucidate whether these compounds reduce cell viability by inducing apoptosis, cell lines MCF-7, PC-3 and DHF were treated with each active compound 12, 13, 17, 21, 22 and 25 and were examined after Hoechst 33342 staining. The compounds 12, 13 and 17 induced apoptosis in various cancer cell lines, as shown by nuclear condensation and/or fragmentation. In addition, it was found that compounds 12 and 13, induced changes in mitochondrial membrane permeability in those cancer cell lines. Such induction was associated with the depletion of mitochondrial membrane potential. These activities led to the cleavage of caspases inducing the cell death process.
从间苯三酚和苔黑酚中获得了16种合成线性衍生物香叶基苯酚,并对其针对癌细胞系(HT-29、PC-3、MDA-MB231、DU-145)和一种非肿瘤细胞系人皮肤成纤维细胞(HDF)进行了体外细胞毒性活性评估。在每种化合物浓度为0 - 100μM的情况下测定72小时的IC50值。化合物12、13、17、21、22和25显示出细胞毒性活性。为了阐明这些化合物是否通过诱导凋亡来降低细胞活力,用每种活性化合物12、13、17、21、22和25处理MCF-7、PC-3和DHF细胞系,并在Hoechst 33342染色后进行检查。化合物12、13和17在各种癌细胞系中诱导凋亡,表现为核浓缩和/或核碎裂。此外,发现化合物12和13在那些癌细胞系中诱导线粒体膜通透性改变。这种诱导与线粒体膜电位的耗竭有关。这些活性导致半胱天冬酶的裂解,从而诱导细胞死亡过程。