Impact TMPRSS2-ERG Molecular Subtype on Prostate Cancer Recurrence

被引:14
作者
Kobelyatskaya, Anastasiya A. [1 ,2 ]
Pudova, Elena A. [1 ]
Snezhkina, Anastasiya, V [1 ]
Fedorova, Maria S. [1 ]
Pavlov, Vladislav S. [1 ]
Guvatova, Zulfiya G. [1 ]
Savvateeva, Maria, V [1 ]
Melnikova, Nataliya, V [1 ]
Dmitriev, Alexey A. [1 ]
Trofimov, Dmitry Y. [3 ]
Sukhikh, Gennady T. [3 ]
Nyushko, Kirill M. [4 ]
Alekseev, Boris Y. [4 ]
Razin, Sergey, V [2 ]
Krasnov, George S. [1 ]
Kudryavtseva, Anna, V [1 ]
机构
[1] Russian Acad Sci, Engelhardt Inst Mol Biol, Moscow 119991, Russia
[2] Russian Acad Sci, Inst Gene Biol, Moscow 119334, Russia
[3] Minist Hlth Russian Federat, Natl Med Res Ctr Obstet, Gynecol & Perinatol, Moscow 117997, Russia
[4] Minist Hlth Russian Federat, Natl Med Res Radiol Ctr, Moscow 125284, Russia
来源
LIFE-BASEL | 2021年 / 11卷 / 06期
基金
俄罗斯科学基金会;
关键词
prostate cancer; TMPRSS2-ERG molecular subtype; tumor recurrence; gene expression; RNA-Seq; BIOCHEMICAL RECURRENCE; EXPRESSION ANALYSIS; GENES; PROGNOSIS; PACKAGE; FUSION; ERG; GNL3;
D O I
10.3390/life11060588
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Currently, seven molecular subtypes of prostate cancer (PCa) are known, the most common of which being the subtype characterized by the presence of the TMPRSS2-ERG fusion transcript. While there is a considerable amount of work devoted to the influence of this transcript on the prognosis of the disease, data on its role in the progression and prognosis of PCa remain controversial. The present study is devoted to the analysis of the association between the TMPRSS2-ERG transcript and the biochemical recurrence of PCa. The study included two cohorts: the RNA-Seq sample of Russian patients with PCa (n = 72) and the TCGA-PRAD data (n = 203). The results of the analysis of the association between the TMPRSS2-ERG transcript and biochemical recurrence were contradictory. The differential expression analysis (biochemical recurrence cases versus biochemical recurrence-free) and the gene set enrichment analysis revealed a list of genes involved in major cellular pathways. The GNL3, QSOX2, SSPO, and SYS1 genes were selected as predictors of the potential prognostic model (AUC = 1.000 for a cohort of Russian patients with PCa and AUC = 0.779 for a TCGA-PRAD cohort).
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页数:11
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