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Restoration of the anti-proliferative and anti-migratory effects of 1,25-dihydroxyvitamin D by silibinin in vitamin D-resistant colon cancer cells

机译:水飞蓟宾对维他命D抗性结肠癌细胞的1,25-二羟基维他命D的抗增殖和抗迁移作用的恢复

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Colorectal carcinoma (CRC) is the third most common cancer in developed countries. A large fraction of cases are linked to chronic intestinal inflammation, with concomitant increased TNF-alpha release and elevated Snail1/Snail2 levels. These transcription factors in turn suppress vitamin D receptor (VDR) expression, resulting in loss of responsiveness to the protective anti-proliferative and anti-migratory effects of 1,25-dihydroxyvitamin D (1,25D). Experimental and epidemiologic evidence support the use of natural products to target CRC. Here we show that the flavonolignan silibinin reverses the TNF-alpha-induced upregulation of Snail1 and Snail2 in the 1,25D-resistant human colon carcinoma cells HT-29. These silibinin effects are accompanied by an increase in VDR levels; Snaill overexpression reverses these silibinin effects. Silibinin also restores promoter activity from a vitamin D-response element (VDRE) reporter construct. While 1,250 had no significant effect on HT-29 and SW480-R cell proliferation and migration, co-treatment with silibinin restored 1,25D responsiveness. In addition, co-treatment with silibinin plus 1,250 decreased proliferation and migration at doses where silibinin alone had no effect. These findings demonstrate that this combination may present a novel approach to target CRC in conditions of chronic colonic inflammation. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
机译:大肠癌(CRC)是发达国家中第三大最常见的癌症。大部分病例与慢性肠道炎症有关,并伴有TNF-α释放增加和Snail1 / Snail2水平升高。这些转录因子反过来会抑制维生素D受体(VDR)的表达,从而导致对1,25-二羟基维生素D(1,25D)的保护性抗增殖和抗迁移作用的响应能力下降。实验和流行病学证据支持使用天然产物靶向CRC。在这里,我们显示了黄素寡糖水飞蓟宾逆转TNF-α诱导的对1,25D耐药的人结肠癌细胞HT-29中Snail1和Snail2的上调。这些水飞蓟宾效应伴随着VDR水平的升高; Snaill过表达逆转了这些水飞蓟宾效应。水飞蓟宾还可以从维生素D反应元件(VDRE)报告基因构建体恢复启动子活性。虽然1,250对HT-29和SW480-R细胞的增殖和迁移没有显着影响,但与水飞蓟宾的共同治疗恢复了1,25D的反应性。此外,与水飞蓟宾加1,250共同治疗可降低仅在水飞蓟宾无效的剂量下的增殖和迁移。这些发现表明,在慢性结肠炎症的情况下,这种组合可能提供靶向CRC的新方法。 (C)2015 Elsevier Ireland Ltd.保留所有权利。

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