Pan-cancer experimental characteristic of human transcriptional patterns connected with telomerase reverse transcriptase (TERT) gene expression status

被引:0
作者
Drobyshev, Aleksey [1 ,2 ]
Modestov, Alexander [2 ]
Suntsova, Maria [1 ,2 ]
Poddubskaya, Elena [2 ,3 ]
Seryakov, Alexander [4 ]
Moisseev, Aleksey [2 ]
Sorokin, Maksim [1 ,2 ]
Tkachev, Victor [5 ]
Zakharova, Galina [2 ]
Simonov, Aleksander [2 ]
Zolotovskaia, Marianna A. [1 ,2 ,6 ]
Buzdin, Anton [1 ,2 ,6 ,7 ]
机构
[1] Endocrinol Res Ctr, Moscow, Russia
[2] IM Sechenov First Moscow State Med Univ, Inst Personalized Oncol, Moscow, Russia
[3] Clin Ctr Vitamed, Moscow, Russia
[4] Med Holding SM Clin, Moscow, Russia
[5] Oncobox LLC, Moscow, Russia
[6] Moscow Ctr Adv Studies 20, Moscow, Russia
[7] Shemyakin & Ovchinnikov Inst Bioorgan Chem, Moscow, Russia
基金
俄罗斯科学基金会;
关键词
TERT promoter C228T and C250T mutations; reverse transcriptase; differential gene expression analysis; RNA sequencing; pathway activation profiling; pan-cancer investigation; MESSENGER-RNA EXPRESSION; PROMOTER MUTATIONS; SYSTEMATIC ANALYSIS; B-CELLS; C-MYC; LENGTH; ACTIVATION; ASSOCIATION; MECHANISM; MAINTENANCE;
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The TERT gene encodes the reverse transcriptase subunit of telomerase and is normally transcriptionally suppressed in differentiated human cells but reactivated in cancers where its expression is frequently associated with poor survival prognosis. Here we experimentally assessed the RNA sequencing expression patterns associated with TERT transcription in 1039 human cancer samples of 27 tumor types. We observed a bimodal distribution of TERT expression where similar to 27% of cancer samples did not express TERT and the rest showed a bell-shaped distribution. Expression of TERT strongly correlated with 1443 human genes including 103 encoding transcriptional factor proteins. Comparison of TERT- positive and negative cancers showed the differential activation of 496 genes and 1975 molecular pathways. Therein, 32/38 (84%) of DNA repair pathways were hyperactivated in TERT+ cancers which was also connected with accelerated replication, transcription, translation, and cell cycle progression. In contrast, the level of 40 positive cell cycle regulator proteins and a set of epithelial-to-mesenchymal transition pathways was specific for the TERT- group suggesting different proliferation strategies for both groups of cancer. Our pilot study showed that the TERT+ group had similar to 13% of cancers with C228T or C250T mutated TERT promoter. However, the presence of promoter mutations was not associated with greater TERT expression compared with other TERT+ cancers, suggesting parallel mechanisms of its transcriptional activation in cancers. In addition, we detected a decreased expression of L1 retrotransposons in the TERT+ group, and further decreased L1 expression in promoter mutated TERT+ cancers. TERT expression was correlated with 17 genes encoding molecular targets of cancer therapeutics and may relate to differential survival patterns of TERT- positive and negative cancers.
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页数:22
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