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花色苷对结直肠癌和乳腺癌的化学预防作用:综述。

Chemopreventive effects of anthocyanins on colorectal and breast cancer: A review.

机构信息

Animal Genetic and Integrative Biology, Université Paris-Saclay, INRAE, AgroParisTech, GABI, 78350, Jouy-en-Josas, France.

College of Life Science, Beijing Institute of Technology, 5 Haidian District, 100811, Beijing, China.

出版信息

Semin Cancer Biol. 2022 Jun;81:241-258. doi: 10.1016/j.semcancer.2020.12.013. Epub 2021 Jan 5.

Abstract

The present review has analyzed the scientific literature, available in the PubMed and Scopus databases, in order to summarize the current state of diet anthocyanin research in breast cancer (BC) and colorectal cancer (CRC) animal models but also for up-to-date human studies. For CRC, 28 preclinical and 9 clinical studies were selected in line with our search query in science databases. In relation to BC, 14 preclinical and 5 clinical studies were selected. Remarkably, all the preclinical studies, to a greater or lesser degree, suggested a chemoprevention effect of anthocyanin in BC/CRC rodent models. These encouraging results from animal models are not extrapolated to the same degree to human studies where, from the similar theoretical daily doses of anthocyanins in these studies, the opposite results were reported. Nevertheless, it is worth mentioning that the anthocyanin doses in the human studies carried out recently are low if we consider the estimated exposure to anthocyanins issued by the European Food Safety Agency (EFSA) or extremely low if we consider with caution the human equivalent dose based on body surface area from the preclinical dosage regimes used. Therefore, although some clinical data has demonstrated an inverse relation between anthocyanin consumption and BC/CRC, this could, in fact, be more relevant if we increase the daily human anthocyanin dose (as observed in animal model dose-effect studies) while new toxicological data for this flavonoid subtype are brought to light.

摘要

本综述分析了 PubMed 和 Scopus 数据库中可获得的科学文献,旨在总结目前关于饮食花色苷在乳腺癌(BC)和结直肠癌(CRC)动物模型中的研究现状,同时也包括最新的人类研究。对于 CRC,根据我们在科学数据库中的搜索查询,共选择了 28 项临床前研究和 9 项临床研究。关于 BC,共选择了 14 项临床前研究和 5 项临床研究。值得注意的是,所有的临床前研究都在不同程度上表明花色苷对 BC/CRC 啮齿动物模型具有化学预防作用。这些令人鼓舞的动物模型研究结果并不能完全外推到人类研究中,因为从这些研究中花色苷的类似理论日剂量来看,报告的结果恰恰相反。然而,值得一提的是,如果我们考虑欧洲食品安全局(EFSA)发布的花色苷估计暴露量,或者如果我们谨慎地考虑基于临床前剂量方案的人体表面积的人体等效剂量,那么最近进行的人类研究中的花色苷剂量是很低的。因此,尽管一些临床数据表明花色苷的消耗与 BC/CRC 呈负相关,但如果我们增加每日人类花色苷剂量(如在动物模型剂量-效应研究中观察到的那样),这种相关性可能会更加显著,同时,这种黄酮类亚型的新毒理学数据也会被揭示出来。

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