TRIM16 transcription factor in prostate cancer

被引:0
|
作者
Spirina, L. V. [1 ,2 ]
Gorbunov, A. K. [1 ]
Kondakova, I. V. [1 ]
Slonimskaya, E. M. [1 ,2 ]
Usynin, E. A. [1 ]
Tarasenko, N. V. [2 ,3 ]
机构
[1] RAS, TNRMC, Canc Res Inst, 5 Kooperativny Str, Tomsk 634050, Russia
[2] SSMU, 2 Moscow Trakt, Tomsk 634050, Russia
[3] RAS, TNRMC, Res Inst Med Genet, 10 Naberezhnaya R Ushayki Str, Tomsk 634050, Russia
来源
BYULLETEN SIBIRSKOY MEDITSINY | 2018年 / 17卷 / 03期
关键词
prostate cancer; transcription factor TRIM16; AR; ER alpha; ER beta;
D O I
10.20538/1682-0363-2018-3-122-130
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of this investigation was to reveal the expression TRIM16, ER alpha, ER beta and AR in prostate cancer tissues compared to benign hyperplasia and clinical and morphological parameters. Materials and methods. Fifty patients with locally advanced prostate cancer with T2-3N0M0 and twenty patients with benign hyperplasia were included in the study. Prostate cancer patients were divided into subgroups according the Gleason score. Nine patients had Gleason score of 6, eighteen patients had 7 Gleason score, seven patients got 8 Gleason score and seven patients got 9 Gleason score. PSA level was from 4 to 100 ng/ml. TRIM16, ER alpha, ER beta and AR expression was determined by PCR in real time. Results. Increase of TRIM16 expression in prostate cancers was accompanied by high AR and ER alpha expression. The onco-suppressor ER beta was not changed in cancer tissues compared to benign hyperplasia. The Gleason score level was dependent on AR/ER beta relation. Associations between the PSA, AR, ER beta and TRIM16 were found in prostate cancers. Conclusion. Transcription factor TRIM16 participated in prostate cancer development. The connection between the ER and AR expression and clinical and morphological factors was found.
引用
收藏
页码:122 / 130
页数:9
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