VEGF-D expression correlates with colorectal cancer aggressiveness and is downregulated by cetuximab

被引:60
作者
Moehler, Markus [1 ]
Firings, Christian [1 ]
Mueller, Annett [1 ]
Gockel, Ines [2 ]
Schimanski, Carl C. [1 ]
Biesterfeld, Stefan [3 ]
Galle, Peter R. [1 ]
Holtmann, Martin H. [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Dept Med 1, D-55101 Mainz, Germany
[2] Johannes Gutenberg Univ Mainz, Dept Gen & Abdominal Surg, D-55101 Mainz, Germany
[3] Johannes Gutenberg Univ Mainz, Inst Pathol, D-55101 Mainz, Germany
关键词
human colorectal cancer; lymphangiogenesis; vascular endothelial growth factor-C; vascular endothelial growth factor-D; epidermal growth factor receptor;
D O I
10.3748/wjg.14.4156
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To gain mechanistic insights into the role played by epidermal growth factor receptor (EGFR) in the regulation of vascular endothelial growth factors (VEGFs) in colorectal cancer (CRC). METHODS: The impact of high-level expression of the growth factor receptors EGFR and VEGF receptor (VEGFR)3 and the VEGFR3 ligands VEGF-C and VEGF-D on disease progression and prognosis in human CRC was investigated in 108 patients using immunohistochemistry. Furthermore, the expression of the lymphangiogenic factors in response to the modulation of EGFR signalling by the EGFR-targeted monoclonal antibody cetuximab was investigated at the mRNA and protein level in human SW480 and SW620 CRC cell lines and a mouse xenograft model. RESULTS: Human CRC specimens and cell lines displayed EGFR, VEGF-C and VEGF-D expression with varying intensities. VEGF-C expression was associated with histological grade. Strong expression of VEGF-D was significantly associated with lymph node metastases and linked to a trend for decreased survival in lymph node-positive patients. EGFR blockade with cetuximab resulted in a significant decrease of VEGF-D expression in vitro and in vivo. CONCLUSION: In conclusion, the expression of VEGF-D in colorectal tumours is significantly associated with lymphatic involvement in CRC patients and such expression might be blocked effectively by cetuximab. (C) 2008 The WIG Press. All rights reserved.
引用
收藏
页码:4156 / 4167
页数:12
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