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低剂量干扰素 α 增强组蛋白去乙酰化酶抑制对前列腺癌细胞生长和侵袭的抗肿瘤潜能。

Low dosed interferon alpha augments the anti-tumor potential of histone deacetylase inhibition on prostate cancer cell growth and invasion.

机构信息

Department of Urology, Goethe-University, Frankfurt am Main, Germany.

出版信息

Prostate. 2012 Dec 1;72(16):1719-35. doi: 10.1002/pros.22525. Epub 2012 Apr 2.

Abstract

We evaluated whether low-dosed interferon alpha (IFNa) may augment the anti-tumor potential of the histone deacetylase (HDAC)-inhibitor valproic acid (VPA) on prostate cancer cells in vitro and in vivo. PC-3, DU-145, or LNCaP prostate cancer cells were treated with VPA (1 mM), IFNa (200 U/ml), or with the VPA-IFNa combination. Tumor cell growth, cell cycle progression, and cell cycle regulating proteins were then investigated by the MTT assay, flow cytometry, and western blotting. Tumor cell adhesion to endothelium or to immobilized extracellular matrix proteins, as well as migratory properties of the cells, were evaluated. Integrin α and β adhesion molecules and alterations of cell signaling pathways were analyzed. Finally, effects of the drug treatment on prostate cancer growth in vivo were determined in the NOD/SCID mouse model. VPA reduced tumor cell adhesion, migration, and growth in vitro. A much stronger anti-cancer potential was evoked by the VPA-IFNa combination, although IFNa in itself did not block growth or adhesion. The same effect was seen when tumor growth was evaluated in vivo. Molecular analysis revealed distinct elevation of histone H3 acetylation caused by VPA which was further up-regulated by VPA-IFNa, whereas IFNa alone did not alter H3 acetylation. The combinatorial benefit became obvious in Akt phosphorylation, p21 and p27 and integrin α1, α3, and β1 expression. Application of low-dosed IFNa to a VPA based regimen profoundly boosts the anti-tumor properties of VPA. The combined use of VPA and low-dosed IFNa may therefore be an innovative option in treating advanced prostate cancer.

摘要

我们评估了低剂量干扰素 α(IFNa)是否可以增强组蛋白去乙酰化酶(HDAC)抑制剂丙戊酸(VPA)对前列腺癌细胞的抗肿瘤潜能,包括体外和体内实验。用 VPA(1mM)、IFNa(200U/ml)或 VPA-IFNa 联合处理 PC-3、DU-145 或 LNCaP 前列腺癌细胞。然后通过 MTT 测定法、流式细胞术和 Western blot 分析肿瘤细胞生长、细胞周期进程和细胞周期调节蛋白。评估肿瘤细胞对内皮细胞或固定细胞外基质蛋白的黏附以及细胞的迁移特性。分析整合素 α 和 β 黏附分子以及细胞信号通路的改变。最后,在 NOD/SCID 小鼠模型中评估药物处理对前列腺癌体内生长的影响。VPA 降低了肿瘤细胞在体外的黏附、迁移和生长。VPA-IFNa 联合使用可产生更强的抗癌潜力,尽管 IFNa 本身并不能阻止生长或黏附。在体内肿瘤生长评估中也观察到了相同的效果。分子分析显示 VPA 引起组蛋白 H3 乙酰化的明显升高,VPA-IFNa 进一步上调了这种升高,而 IFNa 本身不会改变 H3 乙酰化。在 Akt 磷酸化、p21 和 p27 以及整合素 α1、α3 和 β1 表达方面,联合治疗的益处变得明显。将低剂量 IFNa 应用于 VPA 方案可显著增强 VPA 的抗肿瘤特性。因此,联合使用 VPA 和低剂量 IFNa 可能是治疗晚期前列腺癌的一种创新选择。

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