Oncotarget

Research Papers:

NHERF1 regulates the progression of colorectal cancer through the interplay with VEGFR2 pathway

Yanan Gu, Hefen Yu, Chengcheng Hao, Tracey A Martin, Rachel Hargest, Junqi He, Shan Cheng and Wen G Jiang _

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Oncotarget. 2017; 8:7753-7765. https://doi.org/10.18632/oncotarget.13949

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Abstract

Yanan Gu1,2,*, Hefen Yu1,2,*, Chengcheng Hao1,2, Tracey A Martin2,3, Rachel Hargest2,3, Junqi He1,2, Shan Cheng1,2, Wen G Jiang1,2,3

1Department of Biochemistry and Molecular Biology, Capital Medical University, Beijing 100069, China

2Beijing Key Laboratory of Cancer & Metastasis Research, Capital Medical University, Beijing 100069, China

3Cardiff China Medical Research Collaborative, Cardiff University School of Medicine, Heath Park, Cardiff CF14 4XN, UK

*These authors contributed equally to this work

Correspondence to:

Shan Cheng, email: [email protected]

Wen G Jiang, email: [email protected]

Keywords: colorectal cancer, NHERF1, VEGFR, hypoxia, PDZ protein

Received: September 20, 2016     Accepted: December 01, 2016     Published: December 15, 2016

ABSTRACT

The oncogenic role of ectopic expression of Na+/H+ exchanger regulatory factor 1 (NHERF1) was recently suggested in colorectal cancer, where it was implicated in playing a role in the tumor hypoxia microenvironment. Here we showed that a high level expression of NHERF1 was found in colorectal cancer tissues and that the expression of NHERF1 was positively correlated with VEGFR2 expression. The prognostic value of VEGFR2 expression in colorectal cancer relied on the expression of NHERF1. The up-regulation of NHERF1 induced by the exposure to hypoxia in colon cancer cells depended on the activation of VEGFR2 signaling. NHERF1 in turn inhibited the activation of VEGFR2 signaling which could be regulated by the interaction between NHERF1 and VEGFR2, resulting in the reduction of migration and invasion of colon cancer cells. These results suggest a dynamic interplay between NHERF1 and VEGFR2 signaling in colorectal cancer, which could explain the contribution of NHERF1 to the regulation of tumor cell responses to the hypoxia microenvironment.


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