黄酮类化合物木犀草素的抗癌作用。

Anti-carcinogenic effects of the flavonoid luteolin.

作者信息

Seelinger Günter, Merfort Irmgard, Wölfle Ute, Schempp Christoph M

机构信息

Medical and Pharmaceutical Services, Berlin, Germany.

Institute of Pharmaceutical Sciences, Department of Pharmaceutical Biology and Biotechnology, University of Freiburg, Germany.

出版信息

Molecules. 2008 Oct 22;13(10):2628-2651. doi: 10.3390/molecules13102628.

Abstract

Luteolin is a flavonoid which is part of our daily nutrition in relatively low amounts (less than 1 mg/day). Nevertheless, some epidemiological studies suggest an inverse correlation between luteolin intake and the risk of some cancer types. Luteolin displays specific anti-inflammatory and anti-carcinogenic effects, which can only partly be explained by its anti-oxidant and free radical scavenging capacities. Luteolin can delay or block the development of cancer cells in vitro and in vivo by protection from carcinogenic stimuli, by inhibition of tumor cell proliferation, by induction of cell cycle arrest and by induction of apoptosis via intrinsic and extrinsic signaling pathways. When compared to other flavonoids, luteolin was usually among the most effective ones, inhibiting tumor cell proliferation with IC(50) values between 3 and 50 microM in vitro and in vivo by 5 to 10 mg/kg i.p., intragastric application of 0.1-0.3 mg/kg/d, or as food additive in concentrations of 50 to 200 ppm. Luteolin has been shown to penetrate into human skin, making it also a candidate for the prevention and treatment of skin cancer.

摘要

木犀草素是一种黄酮类化合物,在我们日常饮食中的含量相对较低(每天少于1毫克)。然而,一些流行病学研究表明,木犀草素的摄入量与某些癌症类型的风险呈负相关。木犀草素具有特定的抗炎和抗癌作用,但其抗氧化和清除自由基的能力只能部分解释这些作用。木犀草素可以通过抵御致癌刺激、抑制肿瘤细胞增殖、诱导细胞周期停滞以及通过内在和外在信号通路诱导细胞凋亡,在体外和体内延缓或阻止癌细胞的发展。与其他黄酮类化合物相比,木犀草素通常是最有效的之一,在体外和体内通过腹腔注射5至10毫克/千克、每天胃内给药0.1 - 0.3毫克/千克或作为浓度为50至200 ppm的食品添加剂,以3至50微摩尔的半数抑制浓度(IC50)抑制肿瘤细胞增殖。木犀草素已被证明可以渗透到人体皮肤中,这使其也成为预防和治疗皮肤癌的候选物质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb14/6245397/8bfcffe6545c/molecules-13-02628-g001.jpg

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