CXCR4 and SDF-1 Production Are Stimulated by Hepatocyte Growth Factor and Promote Glioma Cell Invasion

Abstract

Background: Hepatocyte growth factor (HGF) and its receptor play an important role in the formation and progression of glioma and can promote tumor proliferation. In this study, we investigated the ability of HGF to promote the proliferation and invasion of U251n cells; we also tested the effects of HGF on stromal cell-derived factor 1 (SDF1) and CXCR4 mRNA expression. Methods: We measured the effect of HGF on the proliferation of U251n cells using enzyme-linked immunosorbent assays (ELISAs) to detect incorporated bromodeoxyuridine (BrdU) as a marker of DNA synthesis. The effects of HGF and SDF-1 on U251n cell invasion and proliferation were measured using the inhibitors K252a to c-Met and AMD3100 to CXCR4. SDF-1 and CXCR4 mRNA and protein expression were measured using quantitative polymerase chain reaction (PCR) and fluorescence-activated cell sorter (FACS) analysis. Small interfering (si)RNAs were also used to down-regulate HGF and c-Met expression in U251n cells. Results: HGF significantly increased U251n cell proliferation and invasion in a dose-dependent manner; K252a blocked this. AMD3100 blocked invasion but not proliferation. CXCR4 and SDF-1 mRNAs were up-regulated when cells were treated with HGF. CXCR4 and SDF-1 mRNA levels and HGF and c-Met protein levels were down-regulated after cells were transfected with siRNAs. Conclusions: HGF has a direct effect on glioma cell proliferation and invasion. HGF up-regulates SDF-1 and CXCR4 mRNA expression and contributes to cell invasion.

CXCR4 antagonist inhibits perineural invasion of adenoid cystic carcinoma

“…The same was observed in the preclinical murine model in which the size of the tumour did not show statistically significant difference between the two groups. The finding is compatible with observation in other studies, in which AMD3100 has been shown to inhibit invasion but not proliferation in other neoplasia 27 28. Although CXCR4 has been associated with tumour growth, CXCR4/SDF-1 interaction has been more implicated with tumour locomotion, invasion and metastasis, which in part can explain the results of our finding.…”

CXCR4 Antagonism Attenuates the Cardiorenal Consequences of Mineralocorticoid Excess

“…One potential explanation is that the decrease in lymphocyte accumulation in AMD3465-treated mice reduced the tissue levels of cytokines, which can upregulate SDF-1. 43 By contrast, there was no change in the expression of SDF1 mRNA in the kidney at 6 weeks. This finding is possibly explained by previous observations in other experimental paradigms that the effect of CXCR4 antagonists on SDF-1 expression appears to be variable over time.…”

Serine Protease Inhibitor Kunitz-Type 2 Is Downregulated in Myelodysplastic Syndromes and Modulates Cell–Cell Adhesion

“…The screening of SDF-1 was carried out by real-time PCR since HGF upregulates SDF-1 mRNA expression [13]. The treatment of nontransduced cells and shControl cells with recombinant HGF resulted in an increased expression of SDF-1 mRNA similar to the shSPINT2 cells (Fig.…”