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用具有抗增殖活性的海洋生物碱阿普亭处理生殖细胞瘤细胞的蛋白质组学分析。

Proteomic profiling of germ cell cancer cells treated with aaptamine, a marine alkaloid with antiproliferative activity.

机构信息

Department of Oncology, Haematology and Bone Marrow Transplantation, Section Pneumology, Hubertus Wald-Tumorzentrum, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

出版信息

J Proteome Res. 2012 Apr 6;11(4):2316-30. doi: 10.1021/pr300170p. Epub 2012 Mar 28.

DOI:10.1021/pr300170p
PMID:22409352
Abstract

Aaptamine is a marine compound isolated from the sponge Aaptos aaptos showing antiproliferative properties via an undefined mode of action. We analyzed the effects of aaptamine treatment on the proliferation and protein expression of the pluripotent human embryonal carcinoma cell line NT2. Effects on proliferation, cell cycle distribution, and induction of apoptosis were analyzed. At lower concentrations, including the IC50 of 50 μM, aaptamine treatment resulted in a G2/M phase cell cycle arrest, whereas at higher concentrations, induction of apoptosis was seen. Differentially expressed proteins were assessed by 2D-PAGE and mass spectrometry, followed by verification and analysis of protein modifications of the most significantly up- and down-regulated proteins. Aaptamine treatment at the IC50 for 48 h resulted in alteration of 10 proteins, of which five each showed up- and down-regulation. Changes in the 2D map were frequently noticed as a result of post-transcriptional modifications, e.g., of the hypusine modification of the eukaryotic initiation factor 5A (eIF5A). Observed alterations such as increased expression of CRABP2 and hypusination of eIF5A have previously been identified during differentiation of pluripotent cells. For the first time, we describe changes in protein expression caused by aaptamine, providing valuable information regarding the mode of action of this compound.

摘要

阿朴胺是一种从海绵 Aaptos aaptos 中分离出来的海洋化合物,具有通过未定义的作用模式抑制增殖的特性。我们分析了阿朴胺处理对多能人胚癌细胞系 NT2 增殖和蛋白质表达的影响。分析了增殖、细胞周期分布和细胞凋亡的诱导。在较低浓度下,包括 50 μM 的 IC50,阿朴胺处理导致 G2/M 期细胞周期阻滞,而在较高浓度下,诱导细胞凋亡。通过 2D-PAGE 和质谱分析评估差异表达蛋白,然后验证和分析最显著上调和下调蛋白的蛋白修饰。阿朴胺处理 48 小时的 IC50 导致 10 种蛋白质发生改变,其中每种蛋白质分别上调和下调。由于转录后修饰,例如真核起始因子 5A (eIF5A) 的 hypusine 修饰,经常注意到 2D 图谱的变化。在多能细胞分化过程中,已经观察到了诸如 CRABP2 表达增加和 eIF5A 的 hypusination 等变化。这是首次描述阿朴胺引起的蛋白质表达变化,为该化合物的作用模式提供了有价值的信息。

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