非小细胞肺癌中EGFR水平与SATB1和emt促进因子的表达相关

IF 1.7 4区 医学 Q4 ONCOLOGY
Natalia Glatzel-Plucinska, Aleksandra Piotrowska, Mateusz Olbromski, Adam Rzechonek, Marzenna Podhorska-Okolow, Piotr Dziegiel
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引用次数: 0

摘要

背景/目的:表皮生长因子受体(EGFR)的表达在非小细胞肺癌(NSCLC)的诊断和治疗中起着关键作用。因此,确定可能影响EGFR水平的因素具有重要意义。有研究表明,Special AT-rich Binding Protein 1 (SATB1)可作为EGFR基因转录的正调控因子;然而,这种关系尚未在非小细胞肺癌中得到证实。本研究的目的是研究临床NSCLC样本中EGFR和SATB1在蛋白和mRNA水平表达之间的潜在关联,并将这些发现与患者的临床病理数据进行评估。材料与方法:研究对象为239例NSCLC临床样本。我们分析了EGFR、SATB1、SLUG、SNAIL、Twist1、N-cadherin、E-cadherin和Ki67蛋白的水平,以及EGFR和SATB1 mrna的表达。方法包括免疫组织化学(IHC)和显色原位杂交(CISH)。结果:NSCLC细胞核中EGFR蛋白表达与SATB1水平(Spearman’s R=0.504, p≤0.0001)、emt促进因子SLUG (R=0.343, p≤0.01)、SNAIL (R=0.129, p≤0.05)、Twist1 (R=0.249, p≤0.001)的表达均呈正相关。在癌细胞细胞质中表达的EGFR蛋白也观察到类似的关系。此外,EGFR mRNA表达与NSCLC患者生存率相关。在腺癌(ACs)中,高EGFR mRNA表达(>0.24 mRNA拷贝/细胞)与较好的总生存率相关(p=0.015),而在鳞状细胞癌(LSCCs)中,高EGFR mRNA表达(>0.05 mRNA拷贝/细胞)与较差的患者预后相关(p=0.046)。结论:NSCLC细胞核和细胞质中EGFR蛋白的表达与SATB1、SLUG、SNAIL、Twist1蛋白的表达呈正相关。EGFR mRNA表达的预后意义取决于肿瘤组织学,在AC和LSCC样本中存在显著差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EGFR Levels in NSCLC Are Associated With Expression of SATB1 and EMT-promoting Factors.

Background/aim: Epidermal growth factor receptor (EGFR) expression plays a key role in the diagnosis and treatment of non-small cell lung cancer (NSCLC). Therefore, identifying factors that may influence EGFR levels is of significant interest. Some studies have suggested that Special AT-rich Binding Protein 1 (SATB1) could act as a positive regulator of EGFR gene transcription; however, this relationship has not yet been confirmed in NSCLC. The aim of this study was to examine the potential association between EGFR and SATB1 expression at both the protein and mRNA levels in clinical NSCLC samples, and to evaluate these findings in relation to patients' clinicopathological data.

Materials and methods: The study was conducted on 239 NSCLC clinical samples. We analyzed the level of EGFR, SATB1, SLUG, SNAIL, Twist1, N-cadherin, E-cadherin, and Ki67 proteins, as well as the expression of EGFR and SATB1 mRNAs. The methods used included immunohistochemistry (IHC) and chromogenic in situ hybridization (CISH).

Results: EGFR protein expression in the nuclei of NSCLC cells was positively associated both with the SATB1 level (Spearman's R=0.504; p≤0.0001) and with the expression of EMT-promoting factors SLUG (R=0.343; p≤0.01), SNAIL (R=0.129; p≤0.05), and Twist1 (R=0.249; p≤0.001). Similar relationships were observed also for the EGFR protein expressed in the cytoplasm of cancer cells. Moreover, it was revealed that EGFR mRNA expression was associated with NSCLC patient survival. In adenocarcinomas (ACs), high EGFR mRNA expression (>0.24 mRNA copies/cell) was correlated with significantly better overall survival (p=0.015), whereas in squamous cell carcinomas (LSCCs), high EGFR mRNA levels (>0.05 mRNA copies/cell) were associated with poor patients' prognosis (p=0.046).

Conclusion: EGFR protein expression in the nuclei and cytoplasm of NSCLC cells was positively associated with the expression of SATB1, SLUG, SNAIL, and Twist1 proteins. The prognostic significance of EGFR mRNA expression was dependent on tumor histology and differed significantly between the AC and LSCC samples.

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来源期刊
Anticancer research
Anticancer research 医学-肿瘤学
CiteScore
3.70
自引率
10.00%
发文量
566
审稿时长
2 months
期刊介绍: ANTICANCER RESEARCH is an independent international peer-reviewed journal devoted to the rapid publication of high quality original articles and reviews on all aspects of experimental and clinical oncology. Prompt evaluation of all submitted articles in confidence and rapid publication within 1-2 months of acceptance are guaranteed. ANTICANCER RESEARCH was established in 1981 and is published monthly (bimonthly until the end of 2008). Each annual volume contains twelve issues and index. Each issue may be divided into three parts (A: Reviews, B: Experimental studies, and C: Clinical and Epidemiological studies). Special issues, presenting the proceedings of meetings or groups of papers on topics of significant progress, will also be included in each volume. There is no limitation to the number of pages per issue.
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