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Identification of new octamer transcription factor 1‐target genes upregulated in castration‐resistant prostate cancer

机译:鉴定在去势抵抗性前列腺癌中上调的新八聚体转录因子1-靶基因

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摘要

Octamer transcription factor 1 ( 1) is an androgen receptor ( )‐interacting partner and regulates the expression of target genes in prostate cancer cells. However, the function of 1 in castration‐resistant prostate cancer ( ) is not fully understood. In the present study, we used 22Rv1 cells as ‐positive model cells to analyze the role of 1 in . We showed that 1 knockdown suppressed cell proliferation and migration of 22Rv1 cells. Using microarray analysis, we identified four and 1‐target genes, disks large‐associated protein 5 ( 5), kinesin family member 15 ( 15), non‐ condensin I complex subunit G ( ), and 80 kinetochore complex component ( 2) in 22Rv1 cells. We observed that knockdown of 5 and 2 suppresses growth and migration of 22Rv1 cells. Furthermore, immunohistochemical analysis showed that positive expression of 5 in prostate cancer specimens is related to poor cancer‐specific survival rates of patients. Notably, enhanced expression of 5 was observed in tissues of patients. Thus, our findings suggest that these four genes regulated by the / 1 complex could have an important role in progression.
机译:Octamer转录因子1(1)是雄激素受体()的相互作用伴侣,调节前列腺癌细胞中靶基因的表达。然而,1在去势抵抗性前列腺癌中的功能尚不完全清楚。在本研究中,我们使用22Rv1细胞作为阳性模型细胞来分析1在血管生成中的作用。我们表明1组合式抑制细胞增殖和22Rv1细胞迁移。通过微阵列分析,我们鉴定了四个和1个靶基因,盘大相关蛋白5(5),驱动蛋白家族成员15(15),非凝集素I复杂亚基G()和80个动粒体复杂成分(2)。 22Rv1细胞。我们观察到敲低5和2抑制22Rv1细胞的生长和迁移。此外,免疫组织化学分析显示,前列腺癌标本中5的阳性表达与患者癌症特异性生存率低有关。值得注意的是,在患者的组织中观察到了5表达的增强。因此,我们的发现表明,受/ 1复合物调节的这四个基因可能在进展中起重要作用。

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