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EZH2 是一种非小细胞肺癌的新型预后生物标志物。

Enhancer of zeste homolog 2 is a novel prognostic biomarker in nonsmall cell lung cancer.

机构信息

Department of Respiratory Medicine, Saitama Medical University International Medical Center, Saitama, Japan.

出版信息

Cancer. 2012 Mar 15;118(6):1599-606. doi: 10.1002/cncr.26441. Epub 2011 Aug 11.

Abstract

BACKGROUND

Enhancer of zeste homolog 2 (EZH2) epigenetically silences many genes through the trimethylation of histone H3 lysine 27 and is implicated in tumor growth, invasion, and metastasis. However, its role in lung cancer has not been well characterized. The objective of the current study was to elucidate the role of EZH2 in nonsmall cell lung cancer (NSCLC) by investigating both clinical samples and cell lines.

METHODS

An immunohistochemical analysis of EZH2 expression was performed in samples from patients with stage I NSCLC to investigate the association of EZH2 expression levels with clinicopathologic variables. An in vitro cell growth assay and a Matrigel invasion assay also were conducted in the EZH2-expressing NSCLC cell lines A549 and H1299 after knocking down EZH2 expression by using an EZH2-specific short-hairpin RNA.

RESULTS

The immunohistochemical analysis classified stage I NSCLC samples (n = 106) into a negative EZH2 expression group (n = 40; 37.7%) and a positive EZH2 expression group (n = 66; 62.3%). Positive EZH2 expression was associated significantly with larger tumor size (P = .014). Kaplan-Meier survival analyses and log-rank tests demonstrated that patients whose samples were classified into the positive EZH2 expression group had a significantly shorter overall survival (P = .015). Experiments in the NSCLC cell lines revealed that the knockdown of EZH2 expression reduced the tumor growth rate and invasive activity.

CONCLUSIONS

The current results indicated that EZH2 promotes progression and invasion of NSCLC, and its expression is a novel prognostic biomarker in NSCLC.

摘要

背景

EZH2 通过组蛋白 H3 赖氨酸 27 的三甲基化使许多基因沉默,从而促进肿瘤生长、侵袭和转移,与肿瘤的发生发展密切相关。然而,EZH2 在非小细胞肺癌(NSCLC)中的作用尚未得到充分的描述。本研究旨在通过研究临床标本和细胞系来阐明 EZH2 在 NSCLC 中的作用。

方法

对 I 期 NSCLC 患者的标本进行 EZH2 表达的免疫组织化学分析,以研究 EZH2 表达水平与临床病理变量的关系。在 EZH2 表达的 NSCLC 细胞系 A549 和 H1299 中,通过 EZH2 特异性短发夹 RNA 敲低 EZH2 表达,进行体外细胞生长测定和 Matrigel 侵袭测定。

结果

免疫组织化学分析将 I 期 NSCLC 标本(n=106)分为 EZH2 阴性表达组(n=40,37.7%)和 EZH2 阳性表达组(n=66,62.3%)。EZH2 阳性表达与肿瘤较大显著相关(P=0.014)。Kaplan-Meier 生存分析和对数秩检验表明,将标本分为 EZH2 阳性表达组的患者总生存率显著降低(P=0.015)。在 NSCLC 细胞系中的实验表明,EZH2 表达的下调降低了肿瘤的生长速度和侵袭活性。

结论

EZH2 促进了 NSCLC 的进展和侵袭,其表达是 NSCLC 的一种新的预后生物标志物。

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