Balam Farinaz Hosseini, Ahmadi Zeinab Sadat, Ghorbani Arman
Student Research Committee, Department of Cellular and Molecular Nutrition, School of Nutrition Sciences & Food Technology, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Student Research Committee, Department of Nutrition, School of Health, Iran University of Medical Sciences, Tehran, Iran.
Heliyon. 2020 Mar 7;6(3):e03557. doi: 10.1016/j.heliyon.2020.e03557. eCollection 2020 Mar.
The cytochrome P450 enzyme functions as the rate-limiting enzyme in changing androgens to estrogens. Inhibition of aromatase is one of the significant objectives of treatment of hormone-dependent diseases such as breast cancer, especially in post-menopausal women. Natural compounds like chrysin, as a flavor that has a high concentration in honey and propolis, are rich sources of them can be useful in inhibiting aromatase for chemoprevention following treatment or in women at risk of acquiring breast cancer. This study intended to summarize the existing evidence on the effect of chrysin on aromatase activity. We systematically searched Science Direct, PubMed and Google Scholar and hand searched the reference lists of identified relevant articles, up to 5 February, 2019. Articles with English abstracts that reported the effect of chrysin on aromatase inhibition and without publication date restriction were investigated. Twenty relevant articles were chosen from a total of 1721 articles. Only one study was performed on humans and two studies were assayed on rats, while other studies were evaluated in vitro. All the studies except one showed that chrysin had the potency of aromatase inhibition; however, only one study performed on endometrial stromal cells showed that chrysin and naringenin did not indicate aromatase inhibitory properties. Various assay methods and experimental conditions were the important aspects leading to different results between the studies. Chrysin has potency in inhibition of the aromatase enzyme and thus can be useful in preventing and treating the hormone-dependent breast cancer and as an adjuvant therapy for estrogen-dependent diseases.
细胞色素P450酶在将雄激素转化为雌激素的过程中起限速酶的作用。抑制芳香化酶是治疗激素依赖性疾病(如乳腺癌)的重要目标之一,尤其是在绝经后女性中。天然化合物如白杨素,作为蜂蜜和蜂胶中高浓度存在的一种成分,是其丰富来源,在治疗后用于化学预防或对有患乳腺癌风险的女性抑制芳香化酶可能有用。本研究旨在总结关于白杨素对芳香化酶活性影响的现有证据。我们系统检索了科学Direct、PubMed和谷歌学术,并人工检索了已识别相关文章的参考文献列表,截至2019年2月5日。对报道了白杨素对芳香化酶抑制作用且无出版日期限制的英文摘要文章进行了研究。从总共1721篇文章中选取了20篇相关文章。仅一项研究是在人体上进行的,两项研究是在大鼠身上测定的,而其他研究是在体外进行评估的。除一项研究外,所有研究均表明白杨素有抑制芳香化酶的能力;然而,仅一项在子宫内膜基质细胞上进行的研究表明白杨素和柚皮素没有显示出芳香化酶抑制特性。各种测定方法和实验条件是导致研究结果不同的重要方面。白杨素有抑制芳香化酶的能力,因此可用于预防和治疗激素依赖性乳腺癌,并作为雌激素依赖性疾病的辅助治疗。