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Stat3 通过上调微小 RNA-370 抑制 Wilms 瘤中 WTX 的表达。

Stat3 inhibits WTX expression through up-regulation of microRNA-370 in Wilms tumor.

机构信息

Department of Surgery, Childrens' Hospital Affiliated to Soochow University, Soochow University, Suzhou 215003, PR China.

出版信息

FEBS Lett. 2013 Mar 18;587(6):639-44. doi: 10.1016/j.febslet.2013.01.012. Epub 2013 Jan 17.

Abstract

Wilms tumor (WT) is a genetically heterogeneous childhood kidney tumor. Several genetic mutations have been identified in WT patients, including inactivation of WTX, somatic stabilizing CTNNB1, and p53 mutations. However, the molecular mechanisms in tumorigenesis remain largely unexplored. Stat3 is a transcription factor that can promote oncogenesis. Stat3 activation is commonly viewed as crucial for multiple tumor proliferation and metastasis. We show that Stat3 is highly activated in Wilms tumor tissues compared to those in adjacent tissues. IL-6 treatment or transfection of a constitutively activated Stat3 in G401 cells promotes cell proliferation. At the molecular level, we further elucidate that Stat3 inhibits WTX expression through up-regulation of microRNA-370. Our results suggest that Stat3/miR-370/WTX regulatory axis might be a critical mechanism in Wilms tumor cells.

摘要

肾母细胞瘤(WT)是一种遗传异质性的儿童肾肿瘤。在 WT 患者中已经鉴定出几种基因突变,包括 WTX 的失活、体细胞稳定 CTNNB1 和 p53 突变。然而,肿瘤发生的分子机制在很大程度上仍未得到探索。Stat3 是一种转录因子,可以促进致癌作用。Stat3 的激活通常被认为对多种肿瘤的增殖和转移至关重要。我们发现,与相邻组织相比,Stat3 在 Wilms 肿瘤组织中高度激活。IL-6 处理或在 G401 细胞中转染组成型激活的 Stat3 可促进细胞增殖。在分子水平上,我们进一步阐明 Stat3 通过上调 microRNA-370 抑制 WTX 的表达。我们的结果表明,Stat3/miR-370/WTX 调节轴可能是 Wilms 肿瘤细胞中的一个关键机制。

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