Choi S H, Kang H K, Im E O, Kim Y J, Bae Y T, Choi Y H, Lee K H, Chung H Y, Chang H K, Kim N D
Department of Pharmacy, Pusan National University, Pusan 609-735, Korea.
Int J Oncol. 2000 Nov;17(5):971-6. doi: 10.3892/ijo.17.5.971.
The effects of retinoic acid (RA) and its analogs, all-trans RA, 9-cis RA and 13-cis RA, were investigated in human breast cancer MCF-7 cells and immortalized breast epithelial cell line MCF-10A. RA inhibited the telomerase activity of MCF-7 cells in a wide range of concentrations. RA at 10 microM also inhibited the growth of MCF-7 cells in a time-dependent manner. However, no significant growth inhibition was found between untreated control and RA-treated MCF-10A cells. Moreover, a marked inhibition of telomerase activity by RA was detected early in MCF-7 cells (after 24 h of RA treatment), which was preceded by a reduction of hTERT mRNA expression (after 12 h of RA treatment). However, MCF-10A cells showed a reduction of telomerase activity and down-regulation of hTERT after 4 days of RA treatment. Simultaneous changes in hTERT mRNA expression and telomerase activity were found for MCF-10A cells. The expressions of hTR and hTEP1 telomerase component genes were not changed after RA treatment. These results indicate that the anti-breast cancer activity of RA could be mediated by its ability to down-regulate the expression of hTERT telomerase gene.
研究了视黄酸(RA)及其类似物全反式视黄酸、9-顺式视黄酸和13-顺式视黄酸对人乳腺癌MCF-7细胞和永生化乳腺上皮细胞系MCF-10A的影响。RA在很宽的浓度范围内抑制MCF-7细胞的端粒酶活性。10 microM的RA也以时间依赖性方式抑制MCF-7细胞的生长。然而,在未处理的对照和经RA处理的MCF-10A细胞之间未发现明显的生长抑制。此外,在MCF-7细胞中(RA处理24小时后)早期检测到RA对端粒酶活性的显著抑制,这之前hTERT mRNA表达降低(RA处理12小时后)。然而,RA处理4天后,MCF-10A细胞显示端粒酶活性降低和hTERT下调。在MCF-10A细胞中发现hTERT mRNA表达和端粒酶活性同时发生变化。RA处理后,hTR和hTEP1端粒酶成分基因的表达没有改变。这些结果表明,RA的抗乳腺癌活性可能是由其下调hTERT端粒酶基因表达的能力介导的。