Wang Weizhang, Zhang Biyu, Chen Hongyuan, Zhang Li
Guangdong Pharmaceutical University, Guangzhou 510006, China.
Zhongguo Zhong Yao Za Zhi. 2010 Feb;35(4):485-8. doi: 10.4268/cjcmm20100417.
To study the anticancer activities of curcumin on human hepatocarcinoma cell line Sk-hep-1 and its related molecular mechanism which has not been elucidated. In the present study,we showed that curcumin inhibited proliferation of Sk-hep-1 cells in a dose-dependent manner through MTF assay. The effect of curcumin on apoptosis in Sk-hep-1 cells was investigated by DAPI staining and the various apoptosis was observed in hepatocarcinoma cell lines Sk-hep-1, HepG2 and Hep3B, but not in normal liver cell line Chang's liver with curcumin treatment. Cell cycle analysis results showed that curcumin treatment resulted in dramatic accumulation of Sk-hep-1 cells at the G0/G1 or G2/M phase. The effect of curcumin on the expression of anti-apoptosis genes (Survivin and BCl-xL) and drug resistance genes (DRG2 and MDR1) was studied by reverse transcription-polymerase chain reaction (RT-PCR). The expression of MDR1 mRNA was significantly decreased in Sk-hep-1 cells treated with curcumin, while no alterations in the amount of DRG2 and anti-apoptosis genes' mRNA levels were found. These results indicate that curcumin is able to inhibit proliferation and induce apoptosis in Sk-hep-1 cells and it may cause by down-regulating the expression of MDR1 mRNA.
为研究姜黄素对人肝癌细胞系Sk-hep-1的抗癌活性及其尚未阐明的相关分子机制。在本研究中,我们通过MTF检测表明姜黄素以剂量依赖性方式抑制Sk-hep-1细胞的增殖。通过DAPI染色研究姜黄素对Sk-hep-1细胞凋亡的影响,在姜黄素处理的肝癌细胞系Sk-hep-1、HepG2和Hep3B中观察到各种凋亡,但在正常肝细胞系Chang's liver中未观察到。细胞周期分析结果表明,姜黄素处理导致Sk-hep-1细胞在G0/G1或G2/M期显著积累。通过逆转录聚合酶链反应(RT-PCR)研究姜黄素对抗凋亡基因(Survivin和BCl-xL)和耐药基因(DRG2和MDR1)表达的影响。在用姜黄素处理的Sk-hep-1细胞中,MDR1 mRNA的表达显著降低,而DRG2和抗凋亡基因的mRNA水平未发现变化。这些结果表明,姜黄素能够抑制Sk-hep-1细胞的增殖并诱导其凋亡,这可能是通过下调MDR1 mRNA的表达所致。