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抗精神病药物氟奋乃静是一种新的 PI3K 抑制剂,也是一种治疗肺癌的潜在抗癌药物。

The antipsychotic agent flupentixol is a new PI3K inhibitor and potential anticancer drug for lung cancer.

机构信息

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

Department of Urology, the 1st Affiliated Hospital of Kunming Medical University, Kunming, China.

出版信息

Int J Biol Sci. 2019 Jun 2;15(7):1523-1532. doi: 10.7150/ijbs.32625. eCollection 2019.

Abstract

: The phosphatidylinositol 3-kinase (PI3K)/AKT signaling pathway is hyperactivated in lung cancer and regulates a broad range of cellular processes, including proliferation, survival, angiogenesis, and metastasis. Thus PI3K is considered a promising target for therapy. To date, PI3K inhibitors have not been approved for lung cancer. Recent studies showed that the antipsychotic agent flupentixol induced apoptosis of lung cancer cell, however the anti-tumor mechanism of flupentixol remains unclear. : (1) The idock software simulated the molecular docking between the PI3Kα protein and flupentixol. (2) Inhibition of PI3Kα by the flupentixol was examined by kinase assays. (3) The cytotoxicity of flupentixol on the NSCLC cell lines was tested by MTT assays. (4) We treated A549 and H661 cells with flupentixol and then measured the percentage of apoptotic cells by the Annexin V/PI analysis. (5) We investigated the effect of flupentixol on the expression of critical PI3K/AKT signaling pathway proteins, further analyzed on the cleavage of PARP and caspase-3 by Western blotting. (6) BALB/C nude mice were subcutaneously injected with A549 cells to evaluate the effect of flupentixol on the growth of lung carcinoma. : Structural analysis of the predicted binding conformation suggested that flupentixol docks to the ATP binding pocket of PI3Kα. Kinase assays demonstrate that flupentixol indeed inhibited the PI3Kα kinase activity. Flupentixol exhibited cytotoxicity in lung cancer cell lines A549 and H661 in a dose- and time-dependent manner. Furthermore, flupentixol more strongly inhibited the phosphorylation of AKT (T308 and S473) and the expression of its downstream target gene Bcl-2 than two known PI3K inhibitors (BYL719 and BKM120). Flupentixol induced apoptosis as measured by PARP and caspase-3 cleavage. Finally, flupentixol significantly suppressed A549 xenograft growth in BALB/C nude mice. : Flupentixol could be docked to the PI3Kα protein and specifically inhibit the PI3K/AKT pathway and survival of lung cancer cells and . As an old drug, flupentixol is a new PI3K inhibitor that may be used for the treatment of lung cancers.

摘要

: 磷脂酰肌醇 3-激酶(PI3K)/AKT 信号通路在肺癌中过度激活,调节多种细胞过程,包括增殖、存活、血管生成和转移。因此,PI3K 被认为是一种有前途的治疗靶点。迄今为止,PI3K 抑制剂尚未被批准用于肺癌。最近的研究表明,抗精神病药氟哌啶醇诱导肺癌细胞凋亡,但其抗肿瘤机制尚不清楚。 : (1) 使用 idock 软件模拟 PI3Kα 蛋白和氟哌啶醇之间的分子对接。(2) 通过激酶测定法检测氟哌啶醇对 PI3Kα 的抑制作用。(3) 通过 MTT 测定法检测氟哌啶醇对 NSCLC 细胞系的细胞毒性。(4) 用氟哌啶醇处理 A549 和 H661 细胞,然后通过 Annexin V/PI 分析测定凋亡细胞的百分比。(5) 通过 Western blot 进一步分析氟哌啶醇对关键 PI3K/AKT 信号通路蛋白表达的影响,分析 PARP 和 caspase-3 的裂解情况。(6) 将 BALB/C 裸鼠皮下注射 A549 细胞,评估氟哌啶醇对肺癌生长的影响。 : 预测结合构象的结构分析表明,氟哌啶醇与 PI3Kα 的 ATP 结合口袋结合。激酶测定表明氟哌啶醇确实抑制了 PI3Kα 激酶活性。氟哌啶醇以剂量和时间依赖的方式在肺癌细胞系 A549 和 H661 中表现出细胞毒性。此外,氟哌啶醇比两种已知的 PI3K 抑制剂(BYL719 和 BKM120)更强烈地抑制 AKT(T308 和 S473)的磷酸化和下游靶基因 Bcl-2 的表达。氟哌啶醇诱导 PARP 和 caspase-3 裂解的细胞凋亡。最后,氟哌啶醇显著抑制 BALB/C 裸鼠中 A549 异种移植物的生长。 : 氟哌啶醇可与 PI3Kα 蛋白结合,并特异性抑制 PI3K/AKT 通路和肺癌细胞的存活。作为一种老药,氟哌啶醇可能成为一种新的 PI3K 抑制剂,用于治疗肺癌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f0e/6643147/e8976a0f6525/ijbsv15p1523g001.jpg

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