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NUB1,一种干扰素诱导蛋白,通过细胞周期调控介导肾细胞癌细胞的抗增殖作用和细胞凋亡。

NUB1, an interferon-inducible protein, mediates anti-proliferative actions and apoptosis in renal cell carcinoma cells through cell-cycle regulation.

机构信息

Department of Urology, Osaka City University Graduate School of Medicine, 1-4-3, Asahimachi, Abeno-ku, Osaka, Japan.

出版信息

Br J Cancer. 2010 Mar 2;102(5):873-82. doi: 10.1038/sj.bjc.6605574. Epub 2010 Feb 16.

Abstract

BACKGROUND

NEDD8 ultimate buster 1 (NUB1) is an interferon (IFN)-inducible protein that downregulates NEDD8 expression and its conjugation system. Although overexpression of NUB1 induces a growth-inhibitory effect in cells, the mechanisms underlying the anti-mitogenic actions of NUB1 in cancer cells remain uncertain. We investigated the anti-cancer effects of NUB1 in human renal cell carcinoma (RCC) cells.

METHODS

Nine human RCC cells were used for this study. The proliferation of RCC cells exposed to IFN-alpha was measured by water-soluble tetrazolium salt assay. The expression level of NUB1 in cells was measured by quantitative reverse transcriptase PCR or western blot analysis. Apoptosis and cell-cycle analysis were performed by flow cytometry. Silencing of NUB1 was performed using a small interfering RNA.

RESULTS

Both NUB1 messenger RNA and protein were significantly induced by IFN-alpha in seven out of nine selected RCC cell lines, and the NUB1 expressions induced by IFN-alpha correlated positively with cell growth inhibition. Overexpression of NUB1 remarkably induced S-phase transition during cell cycle and apoptosis in IFN-alpha-resistant A498 cells, in which NUB1 is not induced by IFN-alpha. The expression levels of two cell-cycle regulator proteins, cyclin E and p27, were increased under the aforementioned conditions. The knockdown of NUB1 enhanced cell proliferation of IFN-alpha-resistant A498 cells and suppressed IFN-alpha-induced growth inhibition in IFN-alpha-sensitive 4TUHR cells.

CONCLUSION

NUB1 may be a key factor involved not only in cell growth inhibition by IFN-alpha in RCC cells but also in the anti-cancer effect against IFN-alpha-resistant RCC cells.

摘要

背景

NEDD8 终极破解酶 1(NUB1)是一种干扰素(IFN)诱导蛋白,可下调 NEDD8 的表达及其缀合系统。虽然 NUB1 的过表达会在细胞中诱导生长抑制作用,但 NUB1 在癌细胞中的抗有丝分裂作用的机制尚不清楚。我们研究了 NUB1 在人肾细胞癌(RCC)细胞中的抗癌作用。

方法

本研究使用了 9 个人 RCC 细胞系。通过水溶性四唑盐法测量暴露于 IFN-α的 RCC 细胞的增殖。通过定量逆转录酶 PCR 或 Western blot 分析测量细胞中 NUB1 的表达水平。通过流式细胞术进行细胞凋亡和细胞周期分析。使用小干扰 RNA 进行 NUB1 沉默。

结果

在 9 个人 RCC 细胞系中,有 7 种细胞系中 IFN-α显著诱导了 NUB1 的信使 RNA 和蛋白表达,IFN-α 诱导的 NUB1 表达与细胞生长抑制呈正相关。过表达 NUB1 可在 IFN-α 耐药的 A498 细胞中显著诱导细胞周期的 S 期转变和细胞凋亡,而 IFN-α 不能诱导 A498 细胞中 NUB1 的表达。在上述情况下,两种细胞周期调节蛋白,细胞周期蛋白 E 和 p27 的表达水平增加。NUB1 的敲低增强了 IFN-α 耐药的 A498 细胞的增殖,并抑制了 IFN-α 敏感的 4TUHR 细胞中 IFN-α 诱导的生长抑制。

结论

NUB1 可能是一个关键因素,不仅参与了 IFN-α 在 RCC 细胞中抑制细胞生长的作用,而且参与了针对 IFN-α 耐药的 RCC 细胞的抗癌作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d42/2833260/fb72b67c6637/6605574f1.jpg

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