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Antiproliferative effect of octreotide on gastric cancer cells mediated by inhibition of Akt/PKB and telomerase

机译:奥曲肽对Akt / PKB和端粒酶抑制作用介导的胃癌细胞增殖抑制作用

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AIM: To investigate the antiproliferative effect of octreotide, a long-acting analogue of somatostatin, on gastric cancer cell line SGC7901 and its possible molecular mechanisms. METHODS: Gastric cancer cell line SGC7901 employed in the study was treated with 0.008, 0.04, 0.2, 1, 5 and 25 μg·ml~(-1) of octreotide respectively for 24 h to evaluate the antiproliferative effect of somatostatin analog on the tumor cells by MTT assay method. To elucidate the underlying mechanism, the cells were exposed to 1 μg·ml~(-1) of octreotide for 0,12, 24 and 48 h, when their Akt/PKB and telomerase activities were respectively determined using PCR-ELSIA and nonradioactive protein kinase assay protocols. The same experimental procedures were also performed in the control cells that were treated with corresponding vehicles instead of somatostatin analog. RESULTS: After exposed to octreotide for 24 h at the concentrations of more than 1 μg·ml~(1-), SGC7901 cells exhibited a dose-dependent inhibition of growth with the inhibiting rate to be as high as 34.66 % when 25 μg·ml~(-1) of octreotide was applied. The Akt/PKB and telomerase activity of SGC7901 cells was significantly inhibited when the cells were exposed to 1 μg·ml~(-1) of octreotide for 12, 24 and 48 h compared with that of their control counterparts (P<0.01), both of which exhibited in a time-dependent manner. CONCLUSION: The antiproliferative effect of octreotide on SGC7901 cells might be mediated by the inhibition of Akt/ PKB and telomerase.
机译:目的:研究生长抑素的长效类似物奥曲肽对胃癌细胞SGC7901的抗增殖作用及其可能的分子机制。方法:分别采用0.008、0.04、0.2、1、5和25μg·ml〜(-1)的奥曲肽对胃癌SGC7901细胞进行24h的处理,以评价生长抑素类似物对肿瘤的抑制作用。 MTT法测定细胞。为了阐明其潜在机制,当分别使用PCR-ELSIA和非放射性蛋白分别测定其Akt / PKB和端粒酶活性时,将细胞暴露于1μg·ml〜(-1)的奥曲肽0.1、12、24和48 h。激酶测定方案。在用相应媒介物代替生长抑素类似物处理的对照细胞中也进行了相同的实验步骤。结果:SGC7901细胞在浓度大于1μg·ml〜(1-)的奥曲肽中暴露24 h后,表现出剂量依赖性的生长抑制作用,当25μg·ml时,抑制率高达34.66%。施加毫升(-1)的奥曲肽。与对照组相比,将SGC7901细胞暴露于1μg·ml〜(-1)的奥曲肽12、24和48 h后,SGC7901细胞的Akt / PKB和端粒酶活性受到显着抑制(P <0.01),两者都显示出时间依赖性。结论:奥曲肽对SGC7901细胞的抗增殖作用可能是通过抑制Akt / PKB和端粒酶介导的。

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