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

被引:67
作者
Bandapalli, Obul R. [1 ]
Ehrmann, Franziska [1 ]
Ehemann, Volker [1 ]
Gaida, Matthias [1 ,2 ]
Macher-Goeppinger, Stephan [1 ]
Wente, Moritz [2 ]
Schirmacher, Peter [1 ]
Brand, Karsten [1 ]
机构
[1] Univ Heidelberg, Dept Gen Pathol, D-69120 Heidelberg, Germany
[2] Univ Heidelberg, Dept Surg, D-69120 Heidelberg, Germany
关键词
Chemokines; Colorectal liver metastasis; CXCL1; Nude mouse; PROSTATE-CANCER CELLS; TISSUE INHIBITOR; CONSTITUTIVE EXPRESSION; GENE-EXPRESSION; INVASION FRONT; CHEMOKINES; MELANOMA; COLON; CARCINOMA; METALLOPROTEINASES-1;
D O I
10.1016/j.cyto.2011.10.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:46 / 53
页数:8
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