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Exploring the Pharmacological Mechanism of Danzhi Xiaoyao Powder on ER-Positive Breast Cancer by a Network Pharmacology Approach

机译:网络药理学方法探讨丹智小涛粉对ER阳性乳腺癌的药理机制

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Background. Breast cancer is the most common malignancy among women worldwide, but the long-term endocrine therapy is frequently associated with adverse side effects. Danzhi Xiaoyao powder (DXP) is a herbal formula that has an effect on breast cancer, especially ER-positive breast cancer. However, the active compounds, potential targets, and pharmacological and molecular mechanism of its action against cancer remain unclear. Methods. A network pharmacology approach comprising drug-likeness evaluation, oral bioavailability prediction, Caco-2 permeability prediction, multiple compound target prediction, multiple known target collection, breast cancer genes collection, and network analysis has been used in this study. Results. Four networks are set up-namely, ER-positive breast cancer network, compound-compound target network of DXP, DXP-ER-positive breast cancer network, and compound-known target-ER-positive breast cancer network. Some ER-positive breast cancer and DXP related targets, clusters, biological processes, and pathways, and several potential anticancer compounds are found. Conclusion. This network analysis successfully predicted, illuminated, and confirmed the molecular synergy of DXP for ER-positive breast cancer, got potential anticancer active compounds, and found the potential ER-positive breast cancer associated targets, cluster, biological processes, and pathways. This work also provides clues to the researcher who explores ethnopharmacological or/and herbal medicine's or even multidrugs' various synergies.
机译:背景。乳腺癌是全世界妇女中最常见的恶性肿瘤,但长期内分泌治疗经常与不良副作用有关。 Danzhi Xiaoyao粉末(DXP)是一种草药配方,对乳腺癌有影响,尤其是ER阳性乳腺癌。然而,其对癌症作用的活性化合物,潜在靶标和药理学和分子机制仍然尚不清楚。方法。在本研究中使用了包含药物肖像评估,口服生物利用度预测,口腔生物利用度预测,CACO-2渗透性预测,多重已知的目标收集,乳腺癌基因集合和网络分析的网络药理学方法。结果。设置了四个网络,即Er阳性乳腺癌网络,DXP,DXP-ER阳性乳腺癌网络和复合靶标靶网络和复合靶标 - 阳性乳腺癌网络。发现一些ER阳性乳腺癌和DXP相关靶,簇,生物过程和途径以及几种潜在的抗癌化合物。结论。该网络分析成功地预测,阐明并确认了DXP对ER阳性乳腺癌的分子协同作用,得到了潜在的抗癌活性化合物,发现潜在的ER阳性乳腺癌相关靶,簇,生物过程和途径。这项工作还为研究人员提供了探索民族科医药或/和草药甚至多药物的各种协同作用的线索。

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