4.3 Article

Gene Expression Signatures in the Peripheral Blood After Radiosurgery of Human Cerebral Arteriovenous Malformations

Journal

STRAHLENTHERAPIE UND ONKOLOGIE
Volume 186, Issue 2, Pages 91-98

Publisher

URBAN & VOGEL
DOI: 10.1007/s00066-010-2034-4

Keywords

Arteriovenous malformation; Radiosurgery; Gene expression; Angiogenesis; Molecular markers

Funding

  1. German Cancer Aid (Deutsche Krebshilfe)
  2. DFG National Priority Research [SPP1190]
  3. NASA NSCOR [NNJ04HJ12G]
  4. German Federal Ministry of Research and Technology [03NU-K004A/C]
  5. Tumor Center Heidelberg-Mannheim

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To unravel biological mechanisms potentially resulting in the obliteration process after radiosurgery (RS) of human cerebral arteriovenous malformations (AVMs) by investigating molecular signatures on the transcriptomic level in peripheral blood of patients. Venous blood samples were obtained at definite points of time before and after RS. The samples were tested for radiation-induced changes regarding biological markers (mRNA) using cDNA and oligo-microarray technology. The corresponding expression profiles were correlated with clinical data and obliteration signs in radiologic imaging. The proof of principle that RS outcome can be successfully correlated with transcriptomics of cellular blood components as disease parameter was demonstrated. The authors identified 76 differentially regulated genes (p < 0.001) after RS. Interestingly, in particular genes with known roles in antiangiogenic and procoagulative pathways were identified as potentially relevant. In particularly, the authors found a significant downregulation of neuropilin-2, protein C inhibitor and cyclin-dependent kinase 6. They also found that low pretreatment blood mRNA levels of TLR4 (toll-like receptor 4) and STAT3 (signal transducer and activator of transcription 3) correlated with fast obliteration of AVMs. The authors report on a novel technique for molecular biological analysis of blood from patients with cerebral AVM treated with RS. Differential regulation of genes in peripheral blood was successfully correlated with RS and time to obliteration of AVMs. The identified genes indicate a potential new methodology to monitor RS, which may result in an individualized therapy and optimized follow-up.

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