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Dual mechanisms for telomerase inhibition in DLD-1 human colorectal adenocarcinoma cells by polyunsaturated fatty acids

机译:多不饱和脂肪酸DLD-1人结肠直肠腺癌细胞端粒酶抑制的双重机制

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Polyunsaturated fatty acids (PUFAs) have been reported to have antitumor activity. In this study, we have tested whether telomerase might be a target for the antitumor effect of fatty acids using DLD-1 colorectal adenocarcinoma cells. In a cell-free approach, fatty acids were added directly to cell lysates, and we confirmed that increasing fatty acid unsaturation correlates with increased inhibition of telomerase activity. Using a cell culture approach, DLD-1 cells were cultured with fatty acids. Ina time and dose dependent manner, EPA and DHA suppressed cellular telomerase activity and the mRNAs encoding hTERT (human telomerase reverse transcriptase) and c-myc. Based on these observations, we suggest that PUFAs inhibit telomerase activity throughdual mechanisms: direct inhibition of enzymatic activity and down regulation of hTERT, one of the telomerase components.
机译:据报道,多不饱和脂肪酸(PUFA)具有抗肿瘤活性。在本研究中,我们测试了端粒酶是否可能是使用DLD-1结直肠腺癌细胞脂肪酸抗肿瘤效应的靶标。在无细胞方法中,将脂肪酸直接加入到细胞裂解物中,并确认增加脂肪酸不饱和度与端粒酶活性的增加相关。使用细胞培养方法,用脂肪酸培养DLD-1细胞。 INA时间和剂量依赖性方式,EPA和DHA抑制细胞端粒酶活性和编码HTERT(人端粒酶逆转录酶)和C-MYC的MRNA。基于这些观察结果,我们表明PUFAS抑制端粒酶活性的通过:直接抑制酶活性和HTERT的下调,其中一种端粒酶组分。

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