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阴-阳 1 通过调控 SOX2OT-SOX2 轴抑制胰腺导管腺癌细胞增殖和肿瘤生长。

Yin Yang-1 suppresses pancreatic ductal adenocarcinoma cell proliferation and tumor growth by regulating SOX2OT-SOX2 axis.

机构信息

Pancreas Center, Department of General Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, PR China; Pancreas Institute of Nanjing Medical University, Nanjing 210029, PR China.

Department of Biochemistry, Nanjing University of Chinese Medicine, Nanjing 210023, PR China.

出版信息

Cancer Lett. 2017 Nov 1;408:144-154. doi: 10.1016/j.canlet.2017.08.032. Epub 2017 Sep 1.

Abstract

The transcription regulator Yin Yang-1 (YY1) serves as a tumor suppressor in pancreatic ductal adenocarcinoma (PDAC). However, the function of YY1 in proliferation of PDAC cells remains to be clarified. In this study, we found that overexpression of YY1 suppressed proliferation and decreased the expression of long non-coding RNA (lncRNA) SOX2OT and its potential target gene SOX2 in PDAC cells. Luciferase reporter, electrophoretic mobility shift (EMSA), and chromatin immunoprecipitation (ChIP) assays revealed binding of YY1 to the SOX2OT promoter. Moreover, YY1 suppressed PDAC cell proliferation through SOX2OT transcriptional inhibition and subsequent decreased SOX2 expression. In addition, YY1 expression was statistically negatively correlated with SOX2OT and SOX2 expression in PDAC tissues and lower level expression of SOX2OT predicted better outcome in PDAC patients. These results confirmed the anti-proliferation effect of YY1 on PDAC cells, which was associated with SOX2 down-regulation in a SOX2OT-dependent mechanism. Although other undiscovered mechanisms may be involved in the YY1-mediated tumor suppression role, the present study suggests that SOX2OT may act as a tumor promotor in PDAC and may represent a valuable diagnostic and therapeutic target.

摘要

转录调节因子 Yin Yang-1(YY1)在胰腺导管腺癌(PDAC)中作为肿瘤抑制因子发挥作用。然而,YY1 在 PDAC 细胞增殖中的功能仍有待阐明。在本研究中,我们发现 YY1 的过表达抑制了 PDAC 细胞的增殖,并降低了长链非编码 RNA(lncRNA)SOX2OT 及其潜在靶基因 SOX2 的表达。荧光素酶报告基因、电泳迁移率变动分析(EMSA)和染色质免疫沉淀(ChIP)实验揭示了 YY1 与 SOX2OT 启动子的结合。此外,YY1 通过抑制 SOX2OT 的转录和随后降低 SOX2 的表达来抑制 PDAC 细胞的增殖。此外,YY1 的表达与 PDAC 组织中 SOX2OT 和 SOX2 的表达呈统计学负相关,并且 SOX2OT 表达水平较低预示着 PDAC 患者的预后较好。这些结果证实了 YY1 对 PDAC 细胞的抗增殖作用,这与 SOX2OT 依赖机制下调 SOX2 有关。尽管 YY1 介导的肿瘤抑制作用可能涉及其他未发现的机制,但本研究表明 SOX2OT 可能在 PDAC 中作为肿瘤促进因子发挥作用,并可能代表有价值的诊断和治疗靶标。

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