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SOX18是子宫颈癌细胞系中刺猬信号通路的一个新靶基因。

SOX18 Is a Novel Target Gene of Hedgehog Signaling in Cervical Carcinoma Cell Lines.

作者信息

Petrovic Isidora, Milivojevic Milena, Popovic Jelena, Schwirtlich Marija, Rankovic Branislava, Stevanovic Milena

机构信息

Laboratory for Human Molecular Genetics, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, P.O.BOX 23, 11000 Belgrade, Serbia.

出版信息

PLoS One. 2015 Nov 20;10(11):e0143591. doi: 10.1371/journal.pone.0143591. eCollection 2015.

Abstract

Although there is much evidence showing functional relationship between Hedgehog pathway, in particular Sonic hedgehog, and SOX transcription factors during embryonic development, scarce data are available regarding their crosstalk in cancer cells. SOX18 protein plays an important role in promoting tumor angiogenesis and therefore emerged as a promising potential target in antiangiogenic tumor therapy. Recently it became evident that expression of SOX18 gene in tumors is not restricted to endothelium of accompanying blood and lymphatic vessels, but in tumor cells as well.In this paper we have identified human SOX18 gene as a novel target gene of Hedgehog signaling in cervical carcinoma cell lines. We have presented data showing that expression of SOX18 gene is regulated by GLI1 and GLI2 transcription factors, final effectors of Hedgehog signaling, and that modulation of Hedgehog signaling activity in considerably influence SOX18 expression. We consider important that Hedgehog pathway inhibitors reduced SOX18 expression, thus showing, for the first time, possibility for manipulationwith SOX18 gene expression. In addition, we analyzed the role of SOX18 in malignant potential of cervical carcinoma cell line, and showed that its overexpression has no influence on cells proliferation and viability, but substantially promotes migration and invasion of cells in vitro. Pro-migratory effect of SOX18 suggests its role in promoting malignant spreading, possibly in response to Hedgehog activation.

摘要

尽管有大量证据表明在胚胎发育过程中刺猬信号通路,尤其是音猬因子,与SOX转录因子之间存在功能关系,但关于它们在癌细胞中的相互作用的数据却很少。SOX18蛋白在促进肿瘤血管生成中起重要作用,因此成为抗血管生成肿瘤治疗中一个有前景的潜在靶点。最近很明显,SOX18基因在肿瘤中的表达不仅限于伴随的血管和淋巴管内皮细胞,在肿瘤细胞中也有表达。在本文中,我们已确定人类SOX18基因是子宫颈癌细胞系中刺猬信号的一个新的靶基因。我们提供的数据表明,SOX18基因的表达受刺猬信号的最终效应因子GLI1和GLI2转录因子调控,并且刺猬信号活性的调节对SOX18表达有显著影响。我们认为重要的是,刺猬信号通路抑制剂降低了SOX18的表达,从而首次表明了调控SOX18基因表达的可能性。此外,我们分析了SOX18在子宫颈癌细胞系恶性潜能中的作用,结果表明其过表达对细胞增殖和活力没有影响,但在体外显著促进了细胞的迁移和侵袭。SOX18的促迁移作用表明它在促进恶性扩散中发挥作用,可能是对刺猬信号激活的反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7d1/4654472/1323a6378cab/pone.0143591.g001.jpg

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