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Pdcd4的作用可能具有细胞类型特异性:有证据表明,dUTPase水平的降低可能有助于其在Bon-1细胞中的肿瘤抑制活性。

The action of Pdcd4 may be cell type specific: evidence that reduction of dUTPase levels might contribute to its tumor suppressor activity in Bon-1 cells.

作者信息

Lankat-Buttgereit Brigitte, Lenschen Barbara, Schmidt Harald, Göke Rüdiger

机构信息

Clinical Research Unit for Gastrointestinal Endocrinology, University Hospital of Giessen and Marburg, Baldingerstrasse, Marburg, Germany.

出版信息

Apoptosis. 2008 Jan;13(1):157-64. doi: 10.1007/s10495-007-0153-x.

Abstract

Pdcd4 (programmed cell death protein 4) was identified as a gene up-regulated during apoptosis and, additionally, seems to have a function as a tumor suppressor. However, there are conflicting data concerning its role in programmed cell death and most results for its action as an inhibitor for neoplastic transformation are derived from experiments with epidermal cells. Therefore, we were interested to investigate if the action of Pdcd4 might be cell type specific. For that purpose we examined the expression of Pdcd4 and several other proteins in various tumor cell lines. We could not find any correlation of Pdcd4 levels and expression of proteins associated with cell cycle and/or apoptosis in different cell lines. Furthermore, we stably transfected two cell lines (Bon-1 and HCT116) to over-express Pdcd4 and analyzed protein expression. Although we found several regulated proteins none of these proteins were affected in both cell lines in the same manner. For instance, dUTPase expression was reduced in Bon-1 cells but not changed in HCT116 cells. This regulation might be important for the sensitivity of cells to anti-cancer drugs like inhibitors of thymidilate synthase. Therefore, we conclude that the function of Pdcd4 might be cell type specific. A role for Pdcd4 in apoptosis or as a tumor suppressor might be limited to certain cell types.

摘要

程序性细胞死亡蛋白4(Pdcd4)被鉴定为在细胞凋亡过程中上调的基因,此外,它似乎还具有肿瘤抑制功能。然而,关于其在程序性细胞死亡中的作用存在相互矛盾的数据,并且其作为肿瘤转化抑制剂作用的大多数结果来自表皮细胞实验。因此,我们感兴趣的是研究Pdcd4的作用是否可能具有细胞类型特异性。为此,我们检测了多种肿瘤细胞系中Pdcd4和其他几种蛋白质的表达。我们未发现不同细胞系中Pdcd4水平与细胞周期和/或凋亡相关蛋白质表达之间存在任何相关性。此外,我们稳定转染了两个细胞系(Bon-1和HCT116)以过表达Pdcd4并分析蛋白质表达。虽然我们发现了几种受调控的蛋白质,但这些蛋白质在两个细胞系中均未以相同方式受到影响。例如,dUTPase表达在Bon-1细胞中降低,但在HCT116细胞中未改变。这种调控可能对细胞对诸如胸苷酸合成酶抑制剂等抗癌药物的敏感性很重要。因此,我们得出结论,Pdcd4的功能可能具有细胞类型特异性。Pdcd4在细胞凋亡或作为肿瘤抑制因子中的作用可能仅限于某些细胞类型。

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