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硝酸益康唑抑制肺癌细胞中的 PI3K 活性并促进其凋亡。

Econazole nitrate inhibits PI3K activity and promotes apoptosis in lung cancer cells.

机构信息

Biomedical Engineering Research Center, Kunming Medical University, Kunming, Yunnan, China.

Department of the second medical oncology, The 3rd Affiliated Hospital of Kunming Medical University, Yunnan Tumor Hospital, Kunming, China.

出版信息

Sci Rep. 2017 Dec 21;7(1):17987. doi: 10.1038/s41598-017-18178-0.

Abstract

The phosphatidylinositol-3-kinase (PI3K)/AKT signaling pathway plays a pivotal role in many cellular processes, including the proliferation, survival and differentiation of lung cancer cells. Thus, PI3K is a promising therapeutic target for lung cancer treatment. In this study, we applied free and open-source protein-ligand docking software, screened 3167 FDA-approved small molecules, and identified putative PI3Kα inhibitors. Among them, econazole nitrate, an antifungal agent, exhibited the highest activity in decreasing cell viability in pathological types of NSCLC cell lines, including H661 (large cell lung cancer) and A549 (adenocarcinoma). Econazole decreased the protein levels of p-AKT and Bcl-2, but had no effect on the phosphorylation level of ERK. It inhibited cell growth and promote apoptosis in a dose-dependent manner. Furthermore, the combination of econazole and cisplatin exhibited additive and synergistic effects in the H661 and A549 lung cancer cell lines, respectively. Finally, we demonstrated that econazole significantly suppressed A549 tumor growth in nude mice. Our findings suggest that econazole is a new PI3K inhibitor and a potential drug that can be used in lung cancer treatment alone or in combination with cisplatin.

摘要

磷脂酰肌醇-3-激酶(PI3K)/AKT 信号通路在许多细胞过程中发挥着关键作用,包括肺癌细胞的增殖、存活和分化。因此,PI3K 是治疗肺癌的一个很有前途的治疗靶点。在这项研究中,我们应用了免费和开源的蛋白质-配体对接软件,筛选了 3167 种已批准的 FDA 小分子药物,确定了潜在的 PI3Kα 抑制剂。其中,硝酸益康唑,一种抗真菌药物,在降低非小细胞肺癌细胞系(包括 H661[大细胞肺癌]和 A549[腺癌])病理类型的细胞活力方面表现出最高的活性。硝酸益康唑降低了 p-AKT 和 Bcl-2 的蛋白水平,但对 ERK 的磷酸化水平没有影响。它以剂量依赖的方式抑制细胞生长并促进细胞凋亡。此外,硝酸益康唑与顺铂联合使用在 H661 和 A549 肺癌细胞系中分别表现出相加和协同作用。最后,我们证明了硝酸益康唑在裸鼠中显著抑制了 A549 肿瘤的生长。我们的研究结果表明,硝酸益康唑是一种新的 PI3K 抑制剂,是一种单独或与顺铂联合治疗肺癌的潜在药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f1/5740072/340d06d5fc5f/41598_2017_18178_Fig1_HTML.jpg

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