Resveratrol reduces the expression of insulin‐like growth factor‐1 and hepatocyte growth factor in stromal cells of women with endometriosis compared with nonendometriotic women

白藜芦醇 肝细胞生长因子 子宫内膜异位症 间质细胞 胰岛素样生长因子 生长因子 内分泌学 生物 内科学 男科 癌症研究 医学 药理学 受体
作者
Tahereh Arablou,Ali‐Akbar Delbandi,Sepideh Khodaverdi,Soheila Arefi,Roya Kolahdouz‐Mohammadi,Sahel Heidari,Tahereh Mohammadi,Naheed Aryaeian
出处
期刊:Phytotherapy Research [Wiley]
卷期号:33 (4): 1044-1054 被引量:37
标识
DOI:10.1002/ptr.6298
摘要

Resveratrol, a phytoalexin polyphenol, has antiproliferative, antiangiogenic, anti‐inflammatory, and antioxidant properties. The present study has assessed the effect of resveratrol treatment on the expression of insulin‐like growth factor‐1 (IGF‐1) and hepatocyte growth factor (HGF) in endometrial stromal cells (ESCs) from women with and without endometriosis. Endometrial tissues were obtained from 40 endometriotic patients and 15 nonendometriotic control women. After the enzymatic digestion, 13 eutopic ESCs (EuESCs), 8 ectopic ESCs (EESCs), and 11 control ESCs (CESCs) were treated with resveratrol (100 μM) for 6, 24, and 48 hr. The gene and protein expressions of IGF‐1 and HGF were measured using real‐time polymerase chain reaction and enzyme‐linked immunosorbent assay methods, respectively. Results showed that resveratrol treatment decreased significantly the gene expression of IGF‐1 and HGF in EuESCs, EESCs, and CESCs ( p < 0.05). The effect of resveratrol treatment on the reduction of IGF‐1 gene expression was statistically more noticeable in EESCs compared with CESCs ( p < 0.05). Also, in the case of HGF gene expression, the reducing effect of resveratrol treatment was statistically more considerable in EESCs compared with EuESCs and CESCs ( p < 0.05 and p < 0.01, respectively). The IGF‐1 and HGF protein production decreased significantly in EuESCs and EESCs ( p < 0.05) but not in CESCs. These findings suggest that resveratrol treatment could reduce the expression of IGF‐1 and HGF in ESCs especially in EESCs, which play a pivotal role in disease progression.

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