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鉴定N10-取代吩恶嗪为Akt信号通路的有效且特异性抑制剂。

Identification of N10-substituted phenoxazines as potent and specific inhibitors of Akt signaling.

作者信息

Thimmaiah Kuntebommanahalli N, Easton John B, Germain Glen S, Morton Christopher L, Kamath Shantaram, Buolamwini John K, Houghton Peter J

机构信息

Department of Chemistry, Western Illinois University, Macomb 61455, USA.

出版信息

J Biol Chem. 2005 Sep 9;280(36):31924-35. doi: 10.1074/jbc.M507057200. Epub 2005 Jul 11.

Abstract

A series of 30 N10-substituted phenoxazines were synthesized and screened as potential inhibitors of Akt. In cellular assays at 5 mum, 17 compounds inhibited insulin-like growth factor 1 (IGF-I)-stimulated phosphorylation of Akt (Ser-473) by at least 50% but did not inhibit IGF-I-stimulated phosphorylation of Erk-1/2 (Thr-202/Tyr-204). Substitutions at the 2-position (Cl or CF3) did not alter inhibitory activity, whereas N10-substitutions with derivatives having acetyl (20B) or morpholino (12B) side chain lost activity compared with propyl or butyl substituents (7B and 14B). Inhibition of Akt phosphorylation was associated with the inhibition of IGF-I stimulation of the mammalian target of rapamycin phosphorylation (Ser-2448 and Ser-2481), phosphorylation of p70 S6 kinase (Thr-389), and ribosomal protein S6 (Ser-235/236) in Rh1, Rh18, and Rh30 cell lines. The two most potent compounds 10-[4'-(N-diethylamino)butyl]-2-chlorophenoxazine (10B) and 10-[4'-[(beta-hydroxyethyl)piperazino]butyl]-2-chlorophenoxazine (15B) (in vitro, IC50 approximately 1-2 microM) were studied further. Inhibition of Akt phosphorylation correlated with inhibition of its kinase activity as determined in vitro after immunoprecipitation. Akt inhibitory phenoxazines did not inhibit the activity of recombinant phosphatidylinositol 3'-kinase, PDK1, or SGK1 but potently inhibited the kinase activity of recombinant Akt and Akt deltaPH, a mutant lacking the pleckstrin homology domain. Akt inhibitory phenoxazines blocked IGF-I-stimulated nuclear translocation of Akt in Rh1 cells and suppressed growth of Rh1, Rh18, and Rh30 cells (IC50 2-5 microM), whereas "inactive" derivatives were > or = 10-fold less potent inhibitors of cell growth. In contrast to rapamycin analogs, Akt inhibitory phenoxazines induced significant levels of apoptosis under serum-containing culture conditions at concentrations of agent consistent with Akt inhibition. Thus, the cellular responses to phenoxazine inhibitors of Akt appear qualitatively different from the rapamycin analogs. Modeling studies suggest inhibitory phenoxazines may bind in the ATP-binding site, although ATP competition studies were unable to distinguish between competitive and noncompetitive inhibition.

摘要

合成了一系列30种N10-取代的吩恶嗪,并作为Akt的潜在抑制剂进行筛选。在5μM的细胞试验中,17种化合物抑制胰岛素样生长因子1(IGF-I)刺激的Akt(Ser-473)磷酸化至少50%,但不抑制IGF-I刺激的Erk-1/2(Thr-202/Tyr-204)磷酸化。2-位(Cl或CF3)的取代不改变抑制活性,而与丙基或丁基取代基(7B和14B)相比,N10-用具有乙酰基(20B)或吗啉代(12B)侧链的衍生物取代则失去活性。Akt磷酸化的抑制与Rh1、Rh18和Rh30细胞系中IGF-I刺激的雷帕霉素哺乳动物靶标磷酸化(Ser-2448和Ser-2481)、p70 S6激酶(Thr-389)和核糖体蛋白S6(Ser-235/236)的抑制相关。对两种最有效的化合物10-[4'-(N-二乙氨基)丁基]-2-氯吩恶嗪(10B)和10-[4'-[(β-羟乙基)哌嗪基]丁基]-2-氯吩恶嗪(15B)(体外,IC50约为1-2μM)进行了进一步研究。免疫沉淀后体外测定,Akt磷酸化的抑制与其激酶活性的抑制相关。Akt抑制性吩恶嗪不抑制重组磷脂酰肌醇3'-激酶、PDK1或SGK1的活性,但能有效抑制重组Akt和Akt deltaPH(一种缺乏普列克底物蛋白同源结构域的突变体)的激酶活性。Akt抑制性吩恶嗪阻断IGF-I刺激的Akt在Rh1细胞中的核转位,并抑制Rh1、Rh18和Rh30细胞的生长(IC50为2-5μM),而“无活性”衍生物对细胞生长的抑制效力则低10倍或更多。与雷帕霉素类似物不同,Akt抑制性吩恶嗪在含血清培养条件下,在与Akt抑制一致的药物浓度下诱导显著水平的细胞凋亡。因此,细胞对Akt的吩恶嗪抑制剂的反应在性质上似乎与雷帕霉素类似物不同。模型研究表明,抑制性吩恶嗪可能结合在ATP结合位点,尽管ATP竞争研究无法区分竞争性抑制和非竞争性抑制。

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