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下调 CXCL1 抑制结直肠肝转移瘤的生长。

Down-regulation of CXCL1 inhibits tumor growth in colorectal liver metastasis.

机构信息

Department of General Pathology, University of Heidelberg, Im Neuenheimer Feld 220/221, 69120 Heidelberg, Germany.

出版信息

Cytokine. 2012 Jan;57(1):46-53. doi: 10.1016/j.cyto.2011.10.019. Epub 2011 Nov 29.

Abstract

As part of ongoing studies to obtain a global picture of invasion related events in colorectal liver metastases, here, we report our findings on gene expression of the pro-angiogenic subgroup of chemokines, the CXCL-ELR+ chemokines. Apart from their pro-angiogenic and chemoattractant function, these chemokines appear to also contribute to tumor cell transformation, growth and invasion. In our nude mouse model of colorectal liver metastases, we found CXCL1,2,3,5 and 8 (IL-8) to be up-regulated in the tumor cells of the invasion front as compared to the tumor cells in the inner parts of the tumor. ShRNA mediated down-regulation of the most prominently up-regulated group member, CXCL1/gro-alpha resulted in inhibition of cell viability, invasion and proliferation. In vivo, down-regulation of CXCL1 resulted in a nearly complete prevention of tumor growth in nude mice. Mechanistically, auto-regulatory mechanisms involving NF-kappaB and Akt appear to be involved in pro-tumorigenic functions of CXCL1.

摘要

作为正在进行的研究的一部分,旨在获得结直肠癌肝转移中与侵袭相关事件的全球图像,在此,我们报告了我们关于促血管生成亚群趋化因子(CXCL-ELR+趋化因子)基因表达的发现。除了它们的促血管生成和趋化作用外,这些趋化因子似乎还促进肿瘤细胞的转化、生长和侵袭。在我们的结直肠癌肝转移裸鼠模型中,与肿瘤内部的肿瘤细胞相比,我们发现 CXCL1、2、3、5 和 8(IL-8)在侵袭前沿的肿瘤细胞中上调。通过 shRNA 介导的最显著上调的群组成员 CXCL1/gro-alpha 的下调导致细胞活力、侵袭和增殖的抑制。在体内,CXCL1 的下调导致裸鼠肿瘤生长几乎完全被阻止。从机制上讲,涉及 NF-κB 和 Akt 的自动调节机制似乎参与了 CXCL1 的促肿瘤发生功能。

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