Granulocyte colony-stimulating factor receptor signals for β 1-integrin expression and adhesion in bladder cancer

Abstract

Objectives To examine the association of granulocyte colony-stimulating factor (G-CSF) and G-CSF receptor (G-CSFR) expression with increased β 1-integrin expression and determine the ability of autocrine G-CSFR signaling to promote bladder cancer cell adhesion by way of β 1-integrin. β 1-integrin is expressed at higher levels in more invasive bladder carcinoma cells and participates in the process of tissue invasion. Cancer cell invasion and metastasis in some ways mimic normal neutrophil behavior. In neutrophils, G-CSF acts through its receptor to enhance adhesion and migration. A significant fraction of bladder carcinoma has been reported to express both G-CSF and G-CSFR. Methods We examined bladder carcinoma tissue samples obtained from segmental or radical cystectomy specimens for expression of G-CSF, G-CSFR, and β 1-integrin using reverse transcriptase-polymerase chain reaction, Western blot, and immunohistochemical methods. We determined the G-CSFR–mediated β 1-integrin adhesion using a static adhesion assay and the bladder cancer cell line 5637. Results Eleven of 14 bladder cancer samples expressed G-CSFR. All 11 G-CSFR positive tumors also expressed G-CSF, and the G-CSF/G-CSFR positive tumors had elevated β 1-integrin protein levels. All but one G-CSFR negative tumor demonstrated low β 1-integrin protein levels. In four G-CSF/G-CSFR positive tumors for which distant urothelium was available for examination, G-CSF, G-CSFR, and β 1-integrin expression was also increased. In the 5637 cell line, we demonstrated G-CSFR–mediated upregulation of β 1-integrin–dependent adhesion to fibronectin and laminin. Conclusions G-CSF/G-CSFR expression in some bladder cancers appears to be an early event during malignant transformation that increases β 1-integrin expression and adhesion and thereby may promote tissue invasion.