紫穗槐中化合物对肿瘤辅助治疗的EGFR和HER2受体抑制作用

Do Thi Hang, Tran Hoang Mai, Le Thi Huong, Do Thi Hong Khanh, Nguyễn Thi Thuy, Nguyen Van Khoi, Nguyen Thi Thanh Binh, Bui Thanh Tung
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摘要

表皮生长因子受体(Epidermal growth factor receptor, EGFR)和人上皮受体2 (Human epithelial receptor 2, HER2)是肺癌、乳腺癌等肿瘤治疗的重要靶点。紫荆是一种具有抑制癌细胞增殖能力的药用植物。在本研究中,我们通过分子对接的方法,评估了西叶草化合物对EGFR和HER2受体的抑制能力。从已发表的植物化学成分中分离得到50个化合物。分子对接结果显示,其抑制EGFR的能力比厄洛替尼高34个化合物,比伊可替尼高7个化合物,比阿尔莫替尼高21个化合物,比奥穆替尼高3个化合物;4种化合物对HER2的抑制能力高于neratinib, 4种化合物可能同时抑制EGFR和HER2受体。通过分析利平斯基五定律和预测药代动力学毒理学参数,得到了两种具有类药物性质的化合物。因此,这两种化合物有潜力成为抑制EGFR和HER2受体治疗癌症的药物,需要进一步研究。关键词:EGFR; HER2;分子对接;
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Study the EGFR and HER2 Receptors Inhibitory Effect of Compounds in Siegesbeckia orientalis L. for Supporting Cancer Treatment
 Epidermal growth factor receptor (EGFR) and Human epithelium receptor 2 (HER2) are important targets in cancer treatment such as lung cancer, breast cancer. Siegesbeckia orientalis L. is a medicinal plant that has the ability to inhibit the proliferation of cancer cells. In this study, we evaluated the ability to inhibit EGFR and HER2 receptors of compounds from the Siegesbeckia orientalis L. by molecular docking method. Based on the published phytochemicals of Siegesbeckia orientalis L., we have collected 50 isolated compounds. Molecular docking results showed that the ability to inhibit EGFR was higher than erlotinib with 34 compounds, higher than icotinib with 7 compounds, higher than almonertinib with 21 compounds, and higher than olmutinib with 3 compounds; 4 compounds with higher ability to inhibit HER2 than neratinib, and 4 compounds may inhibit both EGFR and HER2 receptors simultaneously. Analysis of Lipinski's rule of five and predicting pharmacokinetic - toxicological parameters, we obtained two compounds that have drug-like properties. Therefore, these two compounds have the potential to be drugs that inhibit EGFR and HER2 receptors for cancer treatment and need to be studied further. Keywords EGFR, HER2, Molecular docking, Siegesbeckia orientalis L.      
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