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核干细胞因子的过表达促进口腔鳞状细胞癌的恶性进展并导致预后不良。

Overexpression of nucleostemin contributes to an advanced malignant phenotype and a poor prognosis in oral squamous cell carcinoma.

作者信息

Yoshida R, Nakayama H, Nagata M, Hirosue A, Tanaka T, Kawahara K, Nakagawa Y, Matsuoka Y, Sakata J, Arita H, Hiraki A, Shinohara M, Ito T

机构信息

Department of Oral and Maxillofacial Surgery, Kumamoto University Graduate School of Life Sciences, Honjo 1-1-1, Chuo-ku, Kumamoto 860-8556, Japan.

Department of Pathology and Experimental Medicine, Kumamoto University Graduate School of Life Sciences, Honjo 1-1-1, Chuo-ku, Kumamoto 860-8556, Japan.

出版信息

Br J Cancer. 2014 Dec 9;111(12):2308-15. doi: 10.1038/bjc.2014.539. Epub 2014 Oct 14.

Abstract

BACKGROUND

Nucleostemin (NS) is essential for the maintenance of stem cell properties, the functions of which remain poorly understood in cancer cells. The purpose of this study was to explore the impact of NS on malignancy and its clinical significance in oral squamous cell carcinoma (OSCC) patients.

METHODS

We investigated the effects of NS on the proliferation and invasion of OSCC using NS-overexpressing or -knockdown OSCC cells. We assessed the activation of the STAT3 (signal transducer and activator of transcription 3) signalling pathway and the downstream targets in the cells with different expression levels of NS. An immunohistochemical analysis of NS was also performed in 54 OSCC patients who were treated with preoperative chemoradiotherapy and surgery.

RESULTS

The overexpression of NS significantly enhanced the proliferation and invasive potential of OSCC cells. On the other hand, downregulation of NS suppressed the invasiveness of the cells. The alterations of these malignant phenotypes were associated with the activation of STAT3 signalling and its downstream targets. An immunohistochemical analysis demonstrated that a high NS tumour expression level significantly correlated with an advanced T-stage and N-stage. Furthermore, a Cox regression analysis revealed that the NS status (hazard ratio, 9.09; P=0.002) was a significant progression factor for OSCC patients.

CONCLUSIONS

Our results suggest that targeting NS may provide a promising treatment for highly malignant OSCC.

摘要

背景

核干细胞因子(NS)对于维持干细胞特性至关重要,但其在癌细胞中的功能仍知之甚少。本研究旨在探讨NS对口腔鳞状细胞癌(OSCC)患者恶性程度的影响及其临床意义。

方法

我们使用过表达或敲低NS的OSCC细胞研究NS对OSCC增殖和侵袭的影响。我们评估了不同NS表达水平的细胞中信号转导和转录激活因子3(STAT3)信号通路及其下游靶点的激活情况。还对54例接受术前放化疗和手术治疗的OSCC患者进行了NS的免疫组化分析。

结果

NS的过表达显著增强了OSCC细胞的增殖和侵袭潜能。另一方面,NS的下调抑制了细胞的侵袭性。这些恶性表型的改变与STAT3信号及其下游靶点的激活有关。免疫组化分析表明,NS在肿瘤中的高表达水平与晚期T分期和N分期显著相关。此外,Cox回归分析显示,NS状态(风险比,9.09;P=0.002)是OSCC患者的一个显著进展因素。

结论

我们的结果表明,靶向NS可能为高恶性OSCC提供一种有前景的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b458/4264447/999df031da54/bjc2014539f1.jpg

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