ShRNA-mediated knock-down of CXCL8 inhibits tumor growth in colorectal liver metastasis

被引:32
作者
Kumar, Abhishek [1 ]
Cherukumilli, Madhuri [2 ]
Mahmoudpour, Seyed Hamidreza [1 ,3 ]
Brand, Karsten [4 ]
Bandapalli, Obul Reddy [1 ]
机构
[1] German Canc Res Ctr, Div Mol Genet Epidemiol, Neuenheimer Feld 580, D-69120 Heidelberg, Germany
[2] Mol Med Partnetship Unit DKFZ, Neuenheimer Feld 350, D-69120 Heidelberg, Germany
[3] Johannes Gutenberg Univ Mainz, Univ Med Ctr, IMBEI, Mainz, Germany
[4] Inst Pathol, Neuenheimer Feld 220, D-69120 Heidelberg, Germany
关键词
CXCL8; IL-8; Colorectal cancer; Invasion front; Liver metastasis; CXC chemokines; CXCR2; CANCER CELLS; IN-VITRO; PROSTATE-CANCER; INVASION FRONT; INTERLEUKIN-8; ANGIOGENESIS; EXPRESSION; IL-8; PROGRESSION; APOPTOSIS;
D O I
10.1016/j.bbrc.2018.04.144
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
CXCL8 belongs to proinflammatory chemokines that are predominantly involved in neutrophil chemotaxis and degranulation. Several studies have suggested that secretion of CXCL8 from cancer cells have a profound effect on tumor microenvironment. In this study, in continuation to our previous work of understanding the global picture of invasion related genes in colorectal liver metastases, we clearly show an up-regulation of CXCL8 expression in the tumor cells at the invasion front as compared to the tumor cells in the inner parts of the tumor. Furthermore, ShRNA mediated down-regulation of CXCL8 resulted in inhibition of cell proliferation, viability and invasion in vitro and a near complete growth reduction of tumor in vivo. We showed that CXCL8 secreted by tumor cells at the invasion front were able to promote migration through angiogenesis by upregulating VEGFA and invasion via the AKT/GSK beta/beta-catenin/ MMP7 pathway by upregulating BCL-2 confirming the key role of CXCL8 during tumor progression. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:731 / 737
页数:7
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