In Vitro |
Germanicol (0-100 µM;6 和 24 h) 对 HCT-116 和 HT29 人结肠癌细胞具有选择性、强效和剂量依赖性的细胞毒性,而对人结肠成纤维细胞 CCD-18Co 的细胞毒性较低。Germanicol 以剂量依赖性方式诱导 HCT-116 和 HT29 细胞死亡[1]。 Germanicol (0-100 µM;48 h) 以剂量依赖性方式诱导 HCT-116 结肠癌细胞凋亡[1]。 Germanicol (0-100 µM;0-48 h) 抑制 HCT-116 结肠癌细胞迁移[1]。 Cell Viability Assay[1] Cell Line: Human colon cancer cell lines HCT-116 (colon), HT29 (colon) and Human colon fibroblast (CCD-18Co) Concentration: 0, 5, 10, 20, 40 and 100 µM Incubation Time: 6 h and 24 h Result: Showed insignificant cytotoxicity below 20 μM and exhibited potent and dose-dependent cytotoxic effect on both HCT-116 and HT29 colon cancer cells at higher doses over 40 µM. Apoptosis Analysis[1] Cell Line: HCT-116 colon cancer cells Concentration: 0, 10, 40 and 100 µM Incubation Time: 48 h Result: Induced potent and dose-dependent chromatin condensation, accompanied by subsequent DNA damage. Cell Migration Assay [1] Cell Line: HCT-116 colon cancer cells Concentration: 0, 10, 40 and 100 µM Incubation Time: 0, 12, 24 and 48 h Result: Decreased cell migration tendency.
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