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锌指和同源框 2 抑制肝癌细胞增殖并下调细胞周期蛋白 A 和 E 的表达。

Zinc fingers and homeoboxes 2 inhibits hepatocellular carcinoma cell proliferation and represses expression of Cyclins A and E.

机构信息

Key Laboratory for Experimental Teratology of Ministry of Education and Institute of Immunology, Shandong University School of Medicine, Jinan, Shandong, People's Republic of China.

出版信息

Gastroenterology. 2012 Jun;142(7):1559-70.e2. doi: 10.1053/j.gastro.2012.02.049. Epub 2012 Mar 6.

Abstract

BACKGROUND & AIMS: Zinc-fingers and homeoboxes 2 (ZHX2) represses transcription of several genes associated with liver cancer. However, little is known about the role of ZHX2 in the development of hepatocellular carcinoma (HCC). We investigated the mechanisms by which ZHX2 might affect proliferation of HCC cells.

METHODS

We overexpressed and knocked down ZHX2 in HCC cells and analyzed the effects on proliferation, colony formation, and the cell cycle. We also analyzed the effects of ZHX2 overexpression in growth of HepG2.2.15 tumor xenografts in nude mice. Chromatin immunoprecipitation and luciferase reporter assays were used to measure binding of ZHX2 target promoters. Levels of ZHX2 in HCC samples were evaluated by immunohistochemistry.

RESULTS

ZHX2 overexpression significantly reduced proliferation of HCC cells and growth of tumor xenografts in mice; it led to G1 arrest and reduced levels of Cyclins A and E in HCC cell lines. ZHX2 bound to promoter regions of CCNA2 (which encodes Cyclin A) and CCNE1 (which encodes Cyclin E) and inhibited their transcription. Knockdown of Cyclin A or Cyclin E reduced the increased proliferation mediated by ZHX2 knockdown. Nuclear localization of ZHX2 was required for it to inhibit proliferation of HCC cells in culture and in mice. Nuclear localization of ZHX2 was reduced in human HCC samples, even in small tumors (diameter, <5 cm), compared with adjacent nontumor tissues. Moreover, reduced nuclear levels of ZHX2 correlated with reduced survival times of patients, high levels of tumor microvascularization, and hepatocyte proliferation.

CONCLUSIONS

ZHX2 inhibits HCC cell proliferation by preventing expression of Cyclins A and E, and reduces growth of xenograft tumors in mice. Loss of nuclear ZHX2 might be an early step in the development of HCC.

摘要

背景与目的

锌指和同源盒蛋白 2(ZHX2)抑制与肝癌相关的几个基因的转录。然而,ZHX2 在肝细胞癌(HCC)发展中的作用知之甚少。我们研究了 ZHX2 影响 HCC 细胞增殖的机制。

方法

我们在 HCC 细胞中过表达和敲低 ZHX2,并分析对增殖、集落形成和细胞周期的影响。我们还分析了 ZHX2 过表达对裸鼠 HepG2.2.15 肿瘤异种移植生长的影响。染色质免疫沉淀和荧光素酶报告基因检测用于测量 ZHX2 靶启动子的结合。免疫组织化学评估 HCC 样本中的 ZHX2 水平。

结果

ZHX2 过表达显著降低 HCC 细胞的增殖和小鼠肿瘤异种移植的生长;它导致 G1 期阻滞,并降低 HCC 细胞系中细胞周期蛋白 A 和 E 的水平。ZHX2 结合到 CCNA2(编码细胞周期蛋白 A)和 CCNE1(编码细胞周期蛋白 E)的启动子区域,并抑制它们的转录。敲低细胞周期蛋白 A 或细胞周期蛋白 E 可降低 ZHX2 敲低介导的增殖增加。ZHX2 在培养物中和小鼠中抑制 HCC 细胞增殖需要其核定位。与相邻非肿瘤组织相比,人 HCC 样本中的 ZHX2 核定位减少,甚至在小肿瘤(直径<5cm)中也是如此。此外,核 ZHX2 水平降低与患者生存时间缩短、肿瘤微血管化程度高和肝细胞增殖有关。

结论

ZHX2 通过防止细胞周期蛋白 A 和 E 的表达来抑制 HCC 细胞增殖,并减少小鼠异种移植肿瘤的生长。核 ZHX2 的丢失可能是 HCC 发展的早期步骤。

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