Journal of Neuro-Oncology

, Volume 86, Issue 1, pp 47–53 | Cite as

Production of angiogenic factors by human glioblastoma cells following activation of the G-protein coupled formylpeptide receptor FPR

  • Xiao-Hong Yao
  • Yi-Fang Ping
  • Jian-Hong Chen
  • Dai-Lun Chen
  • Cheng-Ping Xu
  • Jiang Zheng
  • Ji Ming Wang
  • Xiu-Wu Bian
Lab. Investigation-Human/Animal Tissue

Abstract

Activation of the formylpeptide receptor (FPR), a G-protein-coupled receptor, by its chemotactic peptide ligand N-formylmethionyl-leucyl-phenylalanine (fMLF) promotes the directional migration and survival of human glioblastoma cells. fMLF also stimulates glioblastoma cells to produce biologically active VEGF, an important angiogenic factor involved in tumor progression. In this study, we examined the capacity of FPR to regulate the production of another angiogenic factor, the chemokine IL-8 (CXCL8), in addition to its demonstrated ability to induce VEGF secretion by malignant glioma cells. We showed that the human glioblastoma cell line U87 secreted considerable levels of IL-8 (CXCL8) upon stimulation by the FPR agonist peptide fMLF. Tumor cells transfected with small interference (si)RNA targeting FPR failed to produce IL-8 as well as VEGF in response to fMLF. Glioblastoma cells bearing FPR siRNA exhibited reduced rate of tumorigenicity in nude mice and tumors formed by such tumor cells showed less active angiogenesis and lower level expression of both IL-8 and VEGF. These results suggest that FPR plays an important role in the angiogenesis of human malignant gliomas through increasing the production of angiogenic factors by FPR positive tumor cells.

Keywords

Angiogenesis Formylpeptide receptor Glioma Interleukin 8 (IL-8) Vascular endothelial growth factor (VEGF) 

Notes

Acknowledgments

This project was supported by grants from National Natural Science Foundation of China (NSFC, No. 30670804), the National Key Research Project of Basic Sciences of China (973 project, No. 2006CB708503) and the National High Technology Development Program (863 project, No. 2006 AA02Z475).

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Copyright information

© Springer Science+Business Media, LLC 2007

Authors and Affiliations

  • Xiao-Hong Yao
    • 1
  • Yi-Fang Ping
    • 1
  • Jian-Hong Chen
    • 1
  • Dai-Lun Chen
    • 1
  • Cheng-Ping Xu
    • 1
  • Jiang Zheng
    • 2
  • Ji Ming Wang
    • 3
  • Xiu-Wu Bian
    • 1
  1. 1.Institute of Pathology, Southwest HospitalThird Military Medical UniversityChongqingChina
  2. 2.Medical Research Center, Southwest HospitalThird Military Medical UniversityChongqingChina
  3. 3.Laboratory of Molecular Immunoregulation, Cancer and Inflammation Program, Center for Cancer ResearchNational Cancer Institute at FrederickFrederickUSA

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