紫紫素作为表皮生长因子受体抑制剂的筛选

Smitha S. Bhat, S. R, Shashanka K. Prasad
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引用次数: 4

摘要

EGFR在各种癌症的信号级联反应中起关键作用,酪氨酸激酶抑制剂阻断EGFR信号传导。天然产物长期以来一直被用作治疗癌症的候选药物。紫紫素是一种细菌色素,因其具有抗菌、抗利什曼原虫、抗病毒和抗肿瘤等多种生物应用而闻名。计算研究已经得出结论,它可能对胰腺癌、甲状腺癌、结直肠癌和子宫内膜癌等癌症有活性,这表明它可能作为一种广泛的抗癌药物应用。本研究旨在将紫紫素与EGFR蛋白进行分子对接,以确定其EGFR抑制剂的特性,从而开发出一种新的抗癌药物。
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In silico Screening of Violacein as an epidermal growth factor receptor inhibitor
EGFR is a key player in the signalling cascades of various kinds of cancers and tyrosine kinase inhibitors block EGFR signalling. Natural products have long been used as candidates for therapy in the management of cancer. Violacein, a bacterial pigment, has been known for its numerous biological applications such as antimicrobial, antileishmanial, antiviral, as well as antitumoral. Computational studies have concluded that it may have activity against cancers like pancreatic cancer, thyroid cancer, colorectal cancer, and endometrial cancer indicating its potential application as a broad range of anti-cancerous drug. This study aimed to perform the molecular docking of violacein with the EGFR protein to ascertain its EGFR inhibitor property, which could lead to the development of a novel anti-cancer drug.
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