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首页> 外文期刊>Molecular medicine reports >Pro-apoptotic and anti-proliferative effects of 3,3 '-diindolylmethane in nasopharyngeal carcinoma cells via downregulation of telomerase activity
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Pro-apoptotic and anti-proliferative effects of 3,3 '-diindolylmethane in nasopharyngeal carcinoma cells via downregulation of telomerase activity

机译:通过端粒酶活性下调鼻咽癌细胞3,3'-二吲哚基甲烷的促凋亡和抗增殖作用

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The pro-apoptotic and anti-proliferative effects of 3,3'-diindolylmethane (DIM) in various tumor cell types have been widely investigated. The underlying mechanisms were suggested to include cell cycle arrest, cell signaling inhibition and downregulation of the androgen receptor. The present study demonstrated that DIM induced apoptosis and inhibited proliferation in nasopharyngeal carcinoma cells by downregulating the activity of telomerase. The nasopharyngeal carcinoma cell line 5-8F was selected for this purpose. A cell counting kit-8 assay and flow cytometry were performed to detect apoptosis and proliferation of 5-8F cells, respectively, which revealed the pro-apoptotic and anti-proliferative effects of DIM. Telomerase activity was detected using a telomeric repeat amplification protocol assay, which revealed that the telomerase activity was inhibited by DIM in a dose-dependent manner. Reverse transcription polymerase chain reaction was used to detect the mRNA expression levels of human telomerase reverse transcriptase (hTERT) and human telomerase RNA (hTR), and western blot analysis was used to detect the protein expression of hTERT. The results showed that the mRNA and protein expression of hTERT were downregulated in 5-8F cells following treatment with DIM; however, the mRNA expression of hTR remained unchanged, suggesting that hTERT was the target of DIM. To further identify the target, the length of telomeres was continually measured using a telomere length detection kit, revealing that the telomeres were shortened by DIM in an concentration-dependent manner. The present study confirmed that DIM had pro-apoptotic and anti-proliferative effects in nasopharyngeal carcinoma cells by regulating telomerase.
机译:已广泛研究3,3'-二吲哚基甲烷(DIM)的促凋亡和抗增殖作用已被广泛研究。表明潜在的机制包括细胞周期停滞,细胞信号传导抑制和雄激素受体的下调。本研究证明,下调端粒酶活性,暗诱导凋亡和抑制鼻咽癌细胞的增殖。为此目的选择鼻咽癌细胞系5-8F。进行细胞计数试剂盒-8测定和流式细胞术以分别检测5-8°F细胞的细胞凋亡和增殖,揭示了暗淡凋亡和抗增殖的效果。使用直切重复扩增方案测定检测端粒酶活性,这揭示了端粒酶活性以剂量依赖性方式抑制。逆转转录聚合酶链反应用于检测人端粒酶逆转录酶(HTERT)和人端粒酶RNA(HTR)的mRNA表达水平,并且使用Western印迹分析来检测HTERT的蛋白质表达。结果表明,在用暗淡后,在5-8°F细胞中下调HTERT的mRNA和蛋白表达;然而,HTR的mRNA表达保持不变,表明HTERT是昏暗的目标。为了进一步鉴定靶,使用端粒长度检测试剂盒连续测量端粒的长度,揭示通过浓度依赖性方式缩小来缩小端粒。本研究证实,暗淡通过调节端粒酶具有鼻咽癌细胞的促凋亡和抗增殖作用。

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