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Proteomic profiling of cerebrospinal fluid identifies prostaglandin D2 synthase as a putative biomarker for pediatric medulloblastoma: A pediatric brain tumor consortium study

  • Meena U. Rajagopal
  • , Yetrib Hathout
  • , Tobey J. MacDonald
  • , Mark W. Kieran
  • , Sri Gururangan
  • , Susan M. Blaney
  • , Peter Phillips
  • , Roger Packer
  • , Heather Gordish-Dressman
  • , Brian R. Rood

Research output: Contribution to journalArticlepeer-review

57 Scopus citations

Abstract

The aims of this study were to demonstrate the feasibility of centrally collecting and processing high-quality cerebrospinal fluid (CSF) samples for proteomic studies within a multi-center consortium and to identify putative biomarkers for medulloblastoma in CSF. We used 2-DE to investigate the CSF proteome from 33 children with medulloblastoma and compared it against the CSF proteome from 25 age-matched controls. Protein spots were subsequently identified by a combination of in-gel tryptic digestion and MALDI-TOF TOF MS analysis. On average, 160 protein spots were detected by 2-DE and 76 protein spots corresponding to 25 unique proteins were identified using MALDI-TOF. Levels of prostaglandin D2 synthase (PGD2S) were found to be six-fold decreased in the tumor samples versus control samples (p<0.00001). These data were further validated using ELISA. Close examination of PGD2S spots revealed the presence of complex sialylated carbohydrates at residues Asn78 and Asn87. Total PGD2S levels are reduced six-fold in the CSF of children with medulloblastoma most likely representing a host response to the presence of the tumor. In addition, our results demonstrate the feasibility of performing proteomic studies on CSF samples collected from patients at multiple institutions within the consortium setting.

Original languageEnglish
Pages (from-to)935-943
Number of pages9
JournalProteomics
Volume11
Issue number5
DOIs
StatePublished - Mar 5 2011

Keywords

  • 2-DE
  • Biomedicine
  • CSF proteomics
  • Medulloblastoma
  • Prostaglandin synthase

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