黄酮类化合物木犀草素和芹菜素的体内潜在抗癌作用和毒性。

IF 2.3 4区 环境科学与生态学 Q4 ENVIRONMENTAL SCIENCES
Xilin Li, Yuxi Li, Si Chen, Lei Guo, Nan Mei
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引用次数: 0

摘要

木犀草素和芹菜素大量存在于各种蔬菜、水果和草药中,已成为值得注意的治疗应用候选者。传统上认为木犀草素和芹菜素具有抗炎和抗氧化活性,最近在体外和动物模型中证明了它们抑制多种癌症类型癌细胞生长的能力。本文综述了支持木犀草素和芹菜素抗癌作用的体内证据,重点介绍了它们的作用机制。这篇综述涵盖了它们对动物肝癌、肺癌、胃癌、结肠癌、乳腺癌、胰腺癌、前列腺癌和皮肤癌的影响。我们还讨论了木犀草素和芹菜素的毒性。尽管有令人鼓舞的临床前结果,但在临床试验中,木犀草素和芹菜素都没有被证明是有效的抗癌药物。因此,本综述还阐述了目前将黄酮抗癌作用转化为临床成功的挑战,强调需要进一步研究先进的动物模型和适当的给药途径,以增加临床前研究的转化价值。本文综述的目的是增进对木犀草素和芹菜素的抗癌和毒理学作用的了解,而不是作为一种风险评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Potential anticancer effects and toxicity of flavones luteolin and apigenin in vivo.

Luteolin and apigenin, which are abundantly present in various vegetables, fruits, and herbs, have emerged as noteworthy candidates for therapeutic applications. Traditionally recognized for their anti-inflammatory and antioxidant activities, both luteolin and apigenin have recently demonstrated the ability to inhibit cancer cell growth across multiple cancer types in vitro and in animal models. This review provides a comprehensive summary of in vivo evidence supporting the anticancer effects of luteolin and apigenin, highlighting their mechanisms of action. The review encompasses studies on their effects on liver, lung, gastric, colon, breast, pancreatic, prostate, and skin cancers in animals. We also discuss the toxicity profiles of luteolin and apigenin. Despite the encouraging preclinical results, neither luteolin nor apigenin has yet been proven to be an effective agent against cancer in clinical trials. Therefore, this review also addresses the current challenges in translating the promising anticancer effects of flavones into clinical success, emphasizing the need for further research using advanced animal models and appropriate administration routes to increase the translational value of preclinical studies. This literature review aims to enhance understanding of the anticancer and toxicological effects of luteolin and apigenin, rather than serving as a risk assessment.

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CiteScore
4.60
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