Durślewicz Justyna, Jóźwicki Jakub, Klimaszewska-Wiśniewska Anna, Zielińska Aleksandra, Antosik Paulina, Grzanka Dariusz, Braun Marcin
Department of Clinical Pathomorphology, Faculty of Medicine, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University, Torun, Poland.
Department of Pathology, Chair of Oncology, Medical University of Lodz, Lodz, Poland.
Discov Oncol. 2022 Oct 15;13(1):106. doi: 10.1007/s12672-022-00568-0.
The present study aimed to investigate expression levels and prognostic significance of RUVBL1 and HNRNPU in stage I and II non-small-cell lung cancer (NSCLC) patients. Therefore, we evaluated immunohistochemical staining of RUVBL1 and HNRNPU, as well as RNA-seq data from public sources, and the results were evaluated concerning overall survival (OS) and clinicopathological features. We found that RUVBL1 and HNRNPU proteins and mRNA levels were higher in tumor tissues as compared to adjacent/normal tissues. RUVBL1 (p = 0.013) and HNRNPU (p = 0.021) high protein levels were independent prognostic factors for poor OS. Also, the multivariate analysis in the TCGA dataset revealed that high RUVBL1 (p = 0.064) and HNRNPU (p = 0.181) mRNA levels were not significantly associated with prognosis. However, the co-expression status of these markers (R + H +) was independently associated with poor OS both in the TCGA dataset (p = 0.027) and in our cohort (p = 0.001). In conclusion, combined and individual expression of RUVBL1 and HNRNPU proteins, as well as R + H + mRNA status, may serve as potential prognostic biomarkers for NSCLC. This study adds to the previous observations that RUVBL1 and HNRNPU might be novel and promising therapeutic targets and markers for prognostic evaluation.
本研究旨在调查RUVBL1和HNRNPU在I期和II期非小细胞肺癌(NSCLC)患者中的表达水平及预后意义。因此,我们评估了RUVBL1和HNRNPU的免疫组织化学染色以及来自公共数据库的RNA测序数据,并根据总生存期(OS)和临床病理特征对结果进行了评估。我们发现,与癌旁/正常组织相比,肿瘤组织中RUVBL1和HNRNPU蛋白及mRNA水平更高。RUVBL1(p = 0.013)和HNRNPU(p = 0.021)的高蛋白水平是OS较差的独立预后因素。此外,TCGA数据集中的多变量分析显示,RUVBL1(p = 0.064)和HNRNPU(p = 0.181)的高mRNA水平与预后无显著相关性。然而,在TCGA数据集(p = 0.027)和我们的队列(p = 0.001)中,这些标志物的共表达状态(R + H +)均与较差的OS独立相关。总之,RUVBL1和HNRNPU蛋白的联合及单独表达以及R + H + mRNA状态可能作为NSCLC潜在的预后生物标志物。本研究补充了之前的观察结果,即RUVBL1和HNRNPU可能是用于预后评估的新型且有前景的治疗靶点和标志物。