TRIM11 expression in non-small cell lung cancer is associated with poor prognosis

被引:0
|
作者
Kuempers, Christiane [1 ]
Jagomast, Tobias [2 ]
Paulsen, Finn -Ole [1 ,3 ]
Heidel, Carsten [1 ,4 ]
Bohnet, Sabine [2 ]
Schierholz, Stefanie [5 ]
Reischl, Markus [6 ]
Dreyer, Eva [1 ]
Olchers, Till [7 ,9 ]
Kirfel, Jutta
Reck, Martin [1 ,7 ,9 ]
Perner, Sven [8 ]
机构
[1] Univ Hosp Schleswig Holstein, Inst Pathol, Campus Luebeck,Ratzeburger Allee 160,Bldg V50, D-23538 Lubeck, Germany
[2] Univ Hosp Schleswig Holstein, Med Clin 3, Pulmonol, Campus Luebeck, Lubeck, Germany
[3] Univ Med Ctr Hamburg Eppendorf, Dept Oncol Hematol & Bone Marrow Transplantat, Div Pneumol, Hamburg, Germany
[4] Sana Hosp, Dept Haematol & Oncol, Lubeck, Germany
[5] Med Univ Schleswig Holstein, Dept Surg, Campus Luebeck, Lubeck, Germany
[6] Karlsruhe Inst Technol, Inst Automat & Appl Informat, Campus Luebeck, Karlsruhe, Germany
[7] LungenClin Grosshansdorf, Dept Thorac Oncol, Grosshansdorf, Germany
[8] Inst Hematopathol Hamburg, Hamburg, Germany
[9] German Ctr Lung Res DZL, Airway Res Ctr North ARCN, Grosshansdorf, Germany
关键词
TRIM11; NSCLC; Prognostic; Biomarker; Immunohistochemistry; PROMOTES PROLIFERATION; INVASION; MIGRATION; PROTEINS; EMT;
D O I
10.14670/HH-18-647
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
. Background. Despite promising results of targeted therapy approaches, non -small cell lung cancer (NSCLC) remains the leading cause of cancer-related death. Tripartite motif containing 11 (TRIM11) is part of the TRIM family of proteins, playing crucial roles in tumor progression. TRIM11 serves as an oncogene in various cancer types and has been reported to be associated with a poor prognosis. In this study, we aimed to investigate the protein expression of TRIM11 in a large NSCLC cohort and to correlate its expression with comprehensive clinico-pathological data. Methods. Immunohistochemical staining of TRIM11 was performed on a European cohort of NSCLC patients (n=275) including 224 adenocarcinomas and 51 squamous cell carcinomas. Protein expression was categorized according to staining intensity as absent, low, moderate and high. To dichotomize samples, absent and low expression was defined as weak and moderate and high expression was defined as high. Results were correlated with clinico-pathological data. Results. TRIM11 was significantly more highly expressed in NSCLC than in normal lung tissue and significantly more highly expressed in squamous cell carcinomas than in adenocarcinomas. We found a significantly worse 5-year overall survival for patients who highly expressed TRIM11 in NSCLC. Conclusions. High TRIM11 expression is linked with a poor prognosis and might serve as a promising novel prognostic biomarker for NSCLC. Its assessment could be implemented in future routine diagnostic workup.
引用
收藏
页码:437 / 446
页数:10
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