C-FOS/C-JUN转录因子在非小细胞肺癌中的共表达

Cancer diagnosis & prognosis Pub Date : 2025-01-03 eCollection Date: 2025-01-01 DOI:10.21873/cdp.10406
Konstantinos Manios, Aristeidis Chrysovergis, Vasileios Papanikolaou, Evangelos Tsiambas, Maria Adamopoulou, Athanasios Stamatelopoulos, Κonstantinos Vachlas, Sotirios Papouliakos, Pavlos Pantos, George Agrogiannis, Andreas C Lazaris, Efthymios Kyrodimos, Periklis Tomos, Nikolaos Kavantzas
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引用次数: 0

摘要

背景/目的:重要的转录因子,包括c-Fos(基因座:14q24.3)和c-Jun(基因座:1p32-p31),调节细胞稳态,防止异常信号转导到细胞核。它们的过度激活似乎与非小细胞肺癌(nsclc)的侵袭性表型有关。在本研究中,我们的目的是共同分析c-FOS/c-JUN蛋白在一系列非小细胞肺癌中的表达与相应的临床病理特征之间的关系。材料与方法:选择50组石蜡包埋的NSCLC组织切片(n=50),分别包括腺癌(n=25)和鳞状细胞癌(n=25)。对c-FOS/c-JUN标志物进行免疫细胞化学(IHC)检测。还进行了数字图像分析(DIA),以客观地评估所检查蛋白质的相应免疫染色强度水平。结果:所有组织样品均有不同水平的蛋白表达。高染色强度分别为34/50(68%)和24/50(48%)。C-FOS过表达与分期相关(p=0.033),而C-JUN过表达与NSCLC组织类型相关(p=0.05),与最大肿瘤直径相关(p=0.046)。结论:C-FOS/C-JUN共过激活在非小细胞肺癌中经常观察到,在恶性肿瘤表型(晚期,转移潜力增加)的侵袭性中发挥潜在的核心作用。针对这些转录因子的新型药物的开发和实施是基于特定遗传特征和蛋白质谱在非鳞状细胞癌患者中应用靶向治疗策略的一种有希望的方法。
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Impact of C-FOS/C-JUN Transcriptional Factors Co-Expression in Non-small Cell Lung Carcinoma.

Background/aim: Significant transcription factors - including c-Fos (gene locus: 14q24.3) and c-Jun (gene locus: 1p32-p31) - regulate cell homeostasis preventing abnormal signal transduction to nucleus. Their over-activation seems to be associated with an aggressive phenotype in non-small cell lung carcinomas (NSCLCs). In the current study, our aim was to co-analyze c-FOS/c-JUN protein expression in a series of NSCLCs correlating them to the corresponding clinico-pathological features.

Materials and methods: A set of fifty (n=50) paraffin embedded NSCLC tissue sections were selected comprising of adenocarcinomas (n=25) and squamous cell carcinomas (n=25), respectively. Immunocytochemistry (IHC) for the c-FOS/c-JUN markers was implemented. Digital image analysis (DIA) was also performed for evaluating objectively the corresponding immunostaining intensity levels of the examined proteins.

Results: All the examined tissue samples expressed the markers in different protein levels. High staining intensity levels were detected in 34/50 (68%) and 24/50 (48%), respectively. C-FOS over expression was statistically significant correlated to stage (p=0.033), whereas C-JUN over expression was associated with NSCLC histotype (p=0.05) and with maximum tumor diameter (p=0.046).

Conclusion: C-FOS/C-JUN co- over activation is observed frequently in NSCLC, playing potentially a central role in the aggressiveness of the malignancy's phenotype (advanced stage, increased metastatic potential). Development and implementation of novel agents that target these transcription factors is a promising approach for applying targeted therapeutic strategies in NSCC patients based on specific genetic signatures and protein profiles.

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