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黄芩素是黄芩的一种活性成分,它能诱导人结肠癌细胞凋亡,并预防 AOM/DSS 诱导的小鼠结肠癌。

Baicalein, an active component of Scutellaria baicalensis Georgi, induces apoptosis in human colon cancer cells and prevents AOM/DSS-induced colon cancer in mice.

机构信息

Department of Pharmacy, Molecular Inflammation Research Center for Aging Intervention, Pusan National University, Busan, Republic of Korea.

出版信息

Int J Oncol. 2013 Nov;43(5):1652-8. doi: 10.3892/ijo.2013.2086. Epub 2013 Sep 4.

Abstract

Flavonoids have been demonstrated to provide health benefits in humans. Baicalein (5,6,7-trihydroxyflavone) is a phenolic flavonoid compound derived mainly from the root of Scutellaria baicalensis Georgi, a medicinal plant traditionally used in oriental medicine. Baicalein is widely used in Korean and Chinese herbal medicines as anti-inflammatory and anticancer therapy. However, the molecular mechanisms of its activity remain poorly understood and warrant further investigation. This study was performed to investigate the anticancer effect of baicalein on HCT116 human colon cancer cells and the tumor preventing capacity of baicalein on colitis-associated cancer in mice. In in vivo experiments, we induced colon tumors in mice by azoxymethane (AOM) and dextran sulfate sodium (DSS) and evaluated the effects of baicalein on tumor growth. Baicalein treatment on HCT116 cells resulted in a concentration-dependent inhibition of cell growth and induction of apoptotic cell death. The induction of apoptosis was determined by morphological changes and cleavage of poly(ADP-ribose) polymerase. Baicalein also suppressed the activation of NF-κB through PPARγ activation. These results indicate that the anti-inflammatory effects of baicalein may be mediated through PPARγ activation. Finally, administration with baicalein significantly decreased the incidence of tumor formation with inflammation. Our findings suggest that baicalein is one of the candidates for the prevention of inflammation-associated colon carcinogenesis.

摘要

类黄酮已被证明对人类健康有益。黄芩素(5,6,7-三羟基黄酮)是一种酚类黄酮化合物,主要来源于黄芩根,黄芩是一种传统的东方医学药用植物。黄芩素广泛用于韩国和中药中,作为抗炎和抗癌治疗。然而,其活性的分子机制仍知之甚少,需要进一步研究。本研究旨在研究黄芩素对人结肠癌细胞 HCT116 的抗癌作用以及黄芩素对结肠炎相关癌症的肿瘤预防能力。在体内实验中,我们用氧化偶氮甲烷(AOM)和葡聚糖硫酸钠(DSS)诱导小鼠结肠肿瘤,并评估黄芩素对肿瘤生长的影响。黄芩素处理 HCT116 细胞导致细胞生长的浓度依赖性抑制和凋亡细胞死亡的诱导。通过形态变化和多聚(ADP-核糖)聚合酶的裂解来确定凋亡的诱导。黄芩素还通过 PPARγ 激活抑制 NF-κB 的激活。这些结果表明,黄芩素的抗炎作用可能是通过 PPARγ 激活介导的。最后,用黄芩素处理可显著降低伴有炎症的肿瘤形成的发生率。我们的研究结果表明,黄芩素是预防炎症相关结肠癌发生的候选药物之一。

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