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基于网络分析的靶向丝氨酸激酶 1 和丙酮酸激酶 M2 的 对人类癌症的植物化合物筛选:一项研究。

Phytocompounds screening of in terms of human cancer by targeting sphingosine kinase-1 and pyruvate kinase-M2: a study based on analysis.

机构信息

Department of Biochemistry, Faculty of Life Sciences, A.M.U, Aligarh, Uttar Pradesh, India.

出版信息

J Biomol Struct Dyn. 2024 Feb-Mar;42(3):1544-1558. doi: 10.1080/07391102.2023.2212773. Epub 2023 May 17.

Abstract

Cancer is a multifactorial disease that can cause morbidity and mortality in humans. An altered gene expression in cancer leads to a change in the overall activity of the human cell. Overexpression of cancer protein may give a piece of wide information about the specific type of tumor. Sphingosine kinase-1 (SK-1) is a metabolic enzyme that is mainly overexpressed in several types of cancer and other inflammatory diseases. Similarly, pyruvate kinase-M2 (PK-M2) is an important oncogenic ATP-producing glycolytic enzyme that is upregulated in most cancer cells. The phytocompound of medicinal plants such as contains a variety of micronutrients that inhibit the proliferation and activity of tumor cells. In this study, the role of phytocompounds in combating cancer was studied against the model kinase proteins, that is, PK-M2 and SK-1. tool like the PASS-Way2Drug server was used to predict the anticancer properties of phytocompounds. Moreover, the CLC-Pred web server provided the cytotoxicity prediction of chemical compounds against several human cancer cell lines. The pharmacokinetics and toxicity profiles were predicted by the SwissADME and pkCSM software. The binding energies were obtained by molecular docking to confirm the intermolecular interaction of selected phytocompounds with proteins. Consequently, molecular dynamics (MD) simulation confirmed the stability, conformational changes, and dynamic behavior of the kinase proteins complexed with the lead phytocompounds, that is, epicatechin, apigenin, and kaempferol.Communicated by Ramaswamy H. Sarma.

摘要

癌症是一种多因素疾病,可导致人类发病和死亡。癌症中基因表达的改变导致人类细胞整体活性的变化。癌蛋白的过度表达可能提供有关特定类型肿瘤的广泛信息。鞘氨醇激酶-1(SK-1)是一种代谢酶,在几种类型的癌症和其他炎症性疾病中主要过表达。同样,丙酮酸激酶-M2(PK-M2)是一种重要的致癌糖酵解 ATP 产生酶,在大多数癌细胞中上调。药用植物的植物化合物含有多种抑制肿瘤细胞增殖和活性的微量营养素。在这项研究中,研究了植物化合物对抗模型激酶蛋白(即 PK-M2 和 SK-1)的抗癌作用。此外,CLC-Pred 网络服务器提供了针对几种人类癌细胞系的化学化合物的细胞毒性预测。药代动力学和毒性概况通过 SwissADME 和 pkCSM 软件进行预测。通过分子对接获得结合能,以确认所选植物化合物与蛋白质之间的分子间相互作用。因此,分子动力学(MD)模拟证实了与先导植物化合物(即表儿茶素、芹菜素和山奈酚)结合的激酶蛋白的稳定性、构象变化和动态行为。由 Ramaswamy H. Sarma 传达。

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