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Aberrant NRP-1 expression serves as predicator of metastatic endometrial and lung cancers
Author(s) -
Imoh S. Okon,
Ding Ye,
Kathleen A. Coughlan,
Qiongxin Wang,
Ping Song,
Doris M. Benbrook,
Ming-Hui Zou
Publication year - 2015
Publication title -
oncotarget
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.373
H-Index - 127
ISSN - 1949-2553
DOI - 10.18632/oncotarget.6699
Subject(s) - cancer research , medicine , hepatocyte growth factor , neuropilin 1 , endometrial cancer , biomarker , growth factor , in vivo , lung cancer , vascular endothelial growth factor , cell culture , lung , cell growth , receptor , cancer , oncology , biology , vegf receptors , genetics , biochemistry , microbiology and biotechnology
Neuropilin-1 (NRP-1) has emerged as an important driver of tumor-promoting phenotypes of human malignancies. However, incomplete knowledge exists as to how this single-pass transmembrane receptor mediates pleiotropic tumor-promoting functions. The purpose of this study was to evaluate NRP-1 expression and metastatic properties in 94 endometrial cancer and matching serum specimens and in a lung cancer cell line. We found that NRP-1 expression significantly correlated with increased tumoral expression of vascular endothelial growth factor 2 (VEGFR2) and serum levels of hepatocyte growth factor (HGF) and cell growth-stimulating factor (C-GSF). Tumoral NRP-1 also was positively associated with expression of NEDD9, a pro-metastatic protein. In the highly metastatic lung cancer cell line (H1792), stable LKB1 depletion caused increased migration in vitro and accentuated NRP-1 and NEDD9 expression in vivo. Our findings demonstrate that perturbed expression of these targets correlate with metastatic potential of endometrial and lung tumors, providing clinically-relevant biomarker applications for diagnostic and therapeutic targeting.

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