The G Protein-Coupled Receptor GALR2 Promotes Angiogenesis in Head and Neck Cancer

被引：32

作者：

Banerjee, Rajat ^{[1
]}

Van Tubergen, Elizabeth A. ^{[1
]}

Scanlon, Christina S. ^{[1
]}

Vander Broek, Robert ^{[1
]}

Lints, Joel P. ^{[1
]}

Liu, Min ^{[1
]}

Russo, Nickole ^{[1
]}

Inglehart, Ronald C. ^{[1
]}

Wang, Yugang ^{[1
]}

Polverini, Peter J. ^{[1
]}

Kirkwood, Keith L. ^{[3
]}

D'Silva, Nisha J. ^{[1
,2
]}

机构：

[1] Univ Michigan, Sch Dent, Dept Periodont & Oral Med, Ann Arbor, MI 48109 USA

[2] Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA

[3] Med Univ S Carolina, Dept Craniofacial Biol, Columbia, SC USA

来源：

MOLECULAR CANCER THERAPEUTICS | 2014年 / 13卷 / 05期

关键词：

ENDOTHELIAL GROWTH-FACTOR; TUMOR PROGRESSION; CARCINOMA-CELLS; GALANIN; INTERLEUKIN-6; ACTIVATION; INHIBITION; SECRETION; PROLIFERATION; MECHANISMS;

D O I：

10.1158/1535-7163.MCT-13-0904

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Squamous cell carcinoma of the head and neck (SCCHN) is an aggressive disease with poor patient survival. Galanin receptor 2 (GALR2) is a G protein-coupled receptor that induces aggressive tumor growth in SCCHN. The objective of this study was to investigate the mechanism by which GALR2 promotes angiogenesis, a critical oncogenic phenotype required for tumor growth. The impact of GALR2 expression on secretion of proangiogenic cytokines in multiple SCCHN cell lines was investigated by ELISA and in vitro angiogenesis assays. Chemical inhibitor and genetic knockdown strategies were used to understand the key regulators. The in vivo impact of GALR2 on angiogenesis was investigated in mouse xenograft, chick chorioallantoic membrane, and the clinically relevant mouse orthotopic floor-of-mouth models. GALR2 induced angiogenesis via p38-MAPK-mediated secretion of proangiogenic cytokines, VEGF, and interleukin-6 (IL-6). Moreover, GALR2 activated small-GTP-protein, RAP1B, thereby inducing p38-mediated inactivation of tristetraprolin (TTP), which functions to destabilize cytokine transcripts. This resulted in enhanced secretion of proangiogenic cytokines and angiogenesis in vitro and in vivo. In SCCHN cells overexpressing GALR2, inactivation of TTP increased secretion of IL-6 and VEGF, whereas inhibition of p38 activated TTP and decreased cytokine secretion. Here, we report that GALR2 stimulates tumor angiogenesis in SCCHN via p38-mediated inhibition of TTP with resultant enhanced cytokine secretion. Given that p38 inhibitors are in clinical use for inflammatory disorders, GALR2/p38-mediated cytokine secretion may be an excellent target for new adjuvant therapy in SCCHN. (C) 2014 AACR.

引用

页码：1323 / 1333

页数：11

共 56 条

[1] Relationship between circulating serum soluble interleukin-6 receptor and the angiogenic cytokines basic fibroblast growth factor and vascular endothelial growth factor in multiple myeloma [J].