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TRIM59作为一种新型分子生物标志物用于预测非小细胞肺癌患者的预后。

TRIM59 as a novel molecular biomarker to predict the prognosis of patients with NSCLC.

作者信息

Lou Ming, Gao Zhaojia, Zhu Tao, Mao Xiaoliang, Wang Yeming, Yuan Kai, Tong Jichun

机构信息

Department of Thoracic Surgery, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, Jiangsu 213003, P.R. China.

Department of Heart and Lung Disease, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, Jiangsu 213003, P.R. China.

出版信息

Oncol Lett. 2020 Feb;19(2):1400-1408. doi: 10.3892/ol.2019.11199. Epub 2019 Dec 10.

Abstract

As a member of the tripartite motif family, tripartite motif-containing protein 59 (TRIM59) serves as an E3 ubiquitin ligase in various cellular processes, including intracellular signaling, development, apoptosis, protein quality control, innate immunity, autophagy and carcinogenesis. The present study aimed to investigate the expression and prognostic value of TRIM59 in patients with non-small cell lung cancer (NSCLC). Expression of TRIM59 in patients with NSCLC was measured by immunohistochemistry in tissue microarrays. Datasets from The Cancer Genome Atlas (TCGA) were used to further verify the expression level of TRIM59 in NSCLC, lung adenocarcinoma and lung squamous cell carcinoma (LUSC). The prognostic value of TRIM59 in NSCLC was also analyzed. Immunohistochemistry revealed that TRIM59 was primarily located in the cytoplasm of tumor cells. Analysis of TCGA datasets revealed that TRIM59 was more highly expressed in tumor tissues than in normal tissues (P<0.0001). Furthermore, the TRIM59 expression level was associated with tumor differentiation (P=0.012), while no association was observed between TRIM59 expression and any other clinicopathological parameters. However, the average overall survival rate of patients with NSCLC in the high TRIM59 expression group was significantly lower than that in the low expression group (P=0.014), especially in patients with LUSC (P=0.016) and patients with poor differentiation (P=0.033). The multivariate analysis indicated that high TRIM59 expression is an independent prognostic factor in patients with NSCLC (P=0.018) and was associated with poor prognosis in patients with NSCLC. Therefore, TRIM59 may serve as a novel molecular biomarker to predict the prognosis of patients with NSCLC.

摘要

作为三重基序家族的成员,含三重基序蛋白59(TRIM59)在多种细胞过程中作为E3泛素连接酶发挥作用,这些过程包括细胞内信号传导、发育、凋亡、蛋白质质量控制、固有免疫、自噬和肿瘤发生。本研究旨在调查TRIM59在非小细胞肺癌(NSCLC)患者中的表达及预后价值。通过组织芯片免疫组化法检测NSCLC患者中TRIM59的表达。来自癌症基因组图谱(TCGA)的数据集用于进一步验证TRIM59在NSCLC、肺腺癌和肺鳞状细胞癌(LUSC)中的表达水平。还分析了TRIM59在NSCLC中的预后价值。免疫组化显示TRIM59主要位于肿瘤细胞的细胞质中。对TCGA数据集的分析显示,TRIM59在肿瘤组织中的表达高于正常组织(P<0.0001)。此外,TRIM59表达水平与肿瘤分化相关(P=0.012),而未观察到TRIM59表达与任何其他临床病理参数之间存在关联。然而,TRIM59高表达组NSCLC患者的平均总生存率显著低于低表达组(P=0.014),尤其是LUSC患者(P=0.016)和低分化患者(P=0.033)。多因素分析表明,TRIM59高表达是NSCLC患者的独立预后因素(P=0.018),且与NSCLC患者的不良预后相关。因此,TRIM59可能作为预测NSCLC患者预后的新型分子生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/938e/6956412/579372b0ba70/ol-19-02-1400-g00.jpg

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