非小细胞肺癌中马来西亚鞭毛虫K-Ras抑制剂突变的计算机筛选。

Q1 Biochemistry, Genetics and Molecular Biology Advances in Bioinformatics Pub Date : 2014-01-01 Epub Date: 2014-09-21 DOI:10.1155/2014/431696
Ayesha Fatima, H F Yee
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引用次数: 8

摘要

K-ras是全球至少15-25%的非小细胞肺癌病例的致病GTPase。由于马来西亚男性和女性的吸烟习惯,这两种类型的肺癌正在以惊人的速度增加。天然产品总是提供安全有效的替代治疗方法。鞭毛台风(Typhonium flagelliforme)是一种已知具有抗癌特性的当地植物。整个提取物被认为比单个成分更有效。由于K-ras是肺癌的关键蛋白,我们的目标是鉴定可以靶向突变K-ras的植物成分。利用对接策略,已报道的鞭毛霉潜在活性化合物被对接到K-ras蛋白的变构表面口袋和开关区域,以确定可能的抑制剂。所选择的配体对ras-SOS结合表面的开关II和相间区具有高的结合亲和力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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In Silico Screening of Mutated K-Ras Inhibitors from Malaysian Typhonium flagelliforme for Non-Small Cell Lung Cancer.

K-ras is an oncogenic GTPase responsible for at least 15-25% of all non-small cell lung cancer cases worldwide. Lung cancer of both types is increasing with an alarming rate due to smoking habits in Malaysia among men and women. Natural products always offer alternate treatment therapies that are safe and effective. Typhonium flagelliforme or Keladi Tikus is a local plant known to possess anticancer properties. The whole extract is considered more potent than individual constituents. Since K-ras is the key protein in lung cancer, our aim was to identify the constituents of the plant that could target the mutated K-ras. Using docking strategies, reported potentially active compounds of Typhonium flagelliforme were docked into the allosteric surface pockets and switch regions of the K-ras protein to identify possible inhibitors. The selected ligands were found to have a high binding affinity for the switch II and the interphase region of the ras-SOS binding surface.

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来源期刊
Advances in Bioinformatics
Advances in Bioinformatics Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (miscellaneous)
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