碘化丙啶
细胞凋亡
细胞周期
癌细胞
细胞周期检查点
细胞毒性T细胞
膜联蛋白
MTT法
活力测定
细胞生长
生物
化学
分子生物学
程序性细胞死亡
癌症研究
癌症
生物化学
体外
遗传学
作者
Jianru Guo,Qianqian Chen,Christopher Wai-Kei Lam,Wei Zhang
标识
DOI:10.1186/s40659-015-0031-x
摘要
We have investigated the potential anticancer effects of karanjin, a principal furanoflavonol constituent of the Chinese medicine Fordia cauliflora, using cytotoxic assay, cell cycle arrest, and induction of apoptosis in three human cancer cell lines (A549, HepG2 and HL-60 cells). MTT cytotoxic assay showed that karanjin could inhibit the proliferation and viability of all three cancer cells. The induction of cell cycle arrest was observed via a PI (propidium iodide)/RNase Staining Buffer detection kit and analyzed by flow cytometry: karanjin could dose-dependently induce cell cycle arrest at G2/M phase in the three cell lines. Cell apoptosis was assessed by Annexin V-FITC/PI staining: all three cancer cells treated with karanjin exhibited significantly increased apoptotic rates, especially in the percentage of late apoptosis cells. Karanjin can induce cancer cell death through cell cycle arrest and enhance apoptosis. This compound may be effective clinically for cancer pharmacotherapy.
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