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细胞周期蛋白A和细胞周期蛋白依赖性激酶2激酶活性通过肿瘤坏死因子-α和干扰素-α联合治疗被抑制。

Cyclin A and Cdk2 kinase activity are suppressed by combined treatment with tumor necrosis factor-alpha and interferon-alpha.

作者信息

Satomoto K, Haisa M, Naomoto Y, Tanaka N, Orita K

机构信息

First Department of Surgery, Okayama University Medical School, Japan.

出版信息

Biochem Biophys Res Commun. 1995 Aug 24;213(3):1115-21. doi: 10.1006/bbrc.1995.2242.

Abstract

We previously reported that combined treatment with tumor necrosis factor-alpha (TNF-alpha) and interferon-alpha (IFN-alpha) showed a synergistic antitumor effect via regulation of cell cycle progression in the S phase. Here, we investigated the effect of the combined treatment with TNF-alpha and IFN-alpha on cell cycle regulating protein in RPMI 4788 cells. Treatment with TNF-alpha or IFN-alpha alone showed no effect on these proteins, however, the combined treatment showed suppression of cyclin A protein and its associated kinase activity. Furthermore, although the combined treatment inhibited Cdk2 kinase activity, the amount of Cdk2 protein was not affected. These results suggested that TNF-alpha and IFN-alpha work together to suppress cyclin A and Cdk2 kinase activity and to inhibit cell cycle progression in the S phase.

摘要

我们之前报道过,肿瘤坏死因子-α(TNF-α)和干扰素-α(IFN-α)联合治疗通过调控S期细胞周期进程显示出协同抗肿瘤作用。在此,我们研究了TNF-α和IFN-α联合治疗对RPMI 4788细胞中细胞周期调节蛋白的影响。单独使用TNF-α或IFN-α治疗对这些蛋白没有影响,然而,联合治疗显示出对细胞周期蛋白A蛋白及其相关激酶活性的抑制作用。此外,尽管联合治疗抑制了Cdk2激酶活性,但Cdk2蛋白的量并未受到影响。这些结果表明,TNF-α和IFN-α共同作用以抑制细胞周期蛋白A和Cdk2激酶活性,并抑制S期细胞周期进程。

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