Skip to main content
Log in

Radiation-induced Blood–brain Barrier Damage in Astrocytoma: Relation to Elevated Gelatinase B and Urokinase

  • Published:
Journal of Neuro-Oncology Aims and scope Submit manuscript

Abstract

Successful management of brain tumors prolongs life, raising the risk of delayed injury secondary to the treatment. Radiation therapy, a mainstay of brain tumor treatment, can damage the cerebral blood vessels. Acutely a breakdown of the blood–brain barrier (BBB) may be seen, but fibrosis complicates radiation injury in the chronic phase. Matrix metalloproteinases (MMPs) and plasminogen activators are two matrix-degrading proteolytic enzymes, which are induced by radiation. They disrupt the basal lamina around cerebral capillaries and open the BBB. We report a patient with an astrocytoma managed by partial resection and external beam irradiation to maximal tolerable doses. The patient later developed malignant brain edema shortly after stereotactic radiosurgery. Tissue obtained during surgical debulking to control the edema showed very high levels of gelatinase B (92 kDa type IV collagenase) and urokinase-type plasminogen activator (uPA). Tumor cells were absent from the biopsy and subsequent autopsy specimens, but necrosis with fibrosis of the blood vessels was seen. If abnormal matrix enzyme function participates in the expression of radiation injury, then inhibitors to such enzymes may provide one strategy for controlling cerebrovascular damage after therapeutic brain radiation.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Dropcho EJ: Central nervous system injury by therapeutic irradiation. Neurol Clin 9: 969–988, 1991

    PubMed  Google Scholar 

  2. Duffey P, Chari G, Cartlidge NE, ShawPJ: Progressive deterioration of intellect and motor function occurring several decades after cranial irradiation. A new facet in the clinical spectrum of radiation encephalopathy. Arch Neurol 53: 814–818, 1996

    PubMed  Google Scholar 

  3. Al-Mefty O, Kersh JE, Routh A, Smith RR: The long-term side effects of radiation therapy for benign brain tumors in adults. J Neurosurg 73: 502–512, 1990

    PubMed  Google Scholar 

  4. DeAngelis LM, Delattre JY, Posner JB: Radiation-induced dementia in patients cured of brain metastases. Neurology 39: 789–796, 1989

    PubMed  Google Scholar 

  5. Marra A, Giuffre R: Late cerebral radionecrosis. Eur Neurol 1: 234–246, 1968

    PubMed  Google Scholar 

  6. Curnes JT, LasterDW, Ball MR, Moody DM, Witcofski RL: Magnetic resonance imaging of radiation injury to the brain. AJNR 7: 389–394, 1986

    Google Scholar 

  7. Delattre JY, Shapiro WR, Posner JB: Acute effects of lowdose cranial irradiation on regional capillary permeability in experimental brain tumors. J Neurolo Sci 90: 147–153, 1989

    Google Scholar 

  8. Rosenberg GA: Matrix metalloproteinases in brain injury. J Neurotr 12: 833–842, 1995

    Google Scholar 

  9. Matrisian LM: Metalloproteinases and their inhibitors in matrix remodeling. Trends Genet 6: 121–125, 1990

    PubMed  Google Scholar 

  10. Rosenberg GA, Kornfeld M, Estrada E, Kelley RO, Liotta LA, Stetler-Stevenson WG: TIMP-2 reduces proteolytic opening of blood-brain barrier by type IV collagenase. Brain Res 576: 203–207, 1992

    PubMed  Google Scholar 

  11. Reich R, Thompson EW, Iwamoto Y, et al.: Effects of inhibitors of plasminogen activator, serine proteinases, and collagenase IV on the invasion of basement membranes by metastatic cells. Cancer Res 48: 3307–3312, 1988

    PubMed  Google Scholar 

  12. Gijbels K, Galardy RE, Steinman L: Reversal of experimental autoimmune encephalomyelitis with a hydroxamate inhibitor of matrix metalloproteases. J Clin Invest 94: 2177–2182, 1994

    PubMed  Google Scholar 

  13. Rosenberg GA, Navratil M, Barone F, Feuerstein G: Proteolytic cascade enzymes increase in focal cerebral ischemia in rat. J Cereb Blood Flow Metab 16: 360–366, 1996

    PubMed  Google Scholar 

  14. Anthony DC, Ferguson B, Matyzak MK, Miller KM, Esiri MM, Perry VH: Differential matrix metalloproteinase expression in cases of multiple sclerosis and stroke. Neuropathology Appl Neurobiol 23: 406–415, 1997

    Google Scholar 

  15. Perry VH, Anthony DC, Bolton SJ, Brown HC: The bloodbrain barrier and the inflammatory response. Mol Med Today 3: 335–341, 1997

    PubMed  Google Scholar 

  16. Clark AW, Krekoski CA, Bou S-S, Chapman KR, Edwards DR: Increased gelatinase A (MMP-2) and gelatinase B (MMP-9) activities in human brain after focal ischemia. Neurosci Lett 238: 53–56, 1997

    PubMed  Google Scholar 

  17. Yong VW, Kerkoski CA, Forsyth PA, Bell R, Edwards DR: Matrix metalloproteinases and diseases of the CNS. TINS 21: 75–80, 1998

    PubMed  Google Scholar 

  18. Sawaya R, Tofilon PJ, Mohanam S, Ali-Osman F, Liotta LA, Stetler-Stevenson WG, Rao JS: Induction of tissue-type plasminogen activator and 72-kDa type-IV collagenase by ionizing radiation in rat astrocytes. Int J Cancer 56: 214–218, 1994

    PubMed  Google Scholar 

  19. Rosenberg GA, Dencoff JE, McGuire PG, Liotta LA, Stetler-Stevenson WG: Injury-induced 92-kDa gelatinase and urokinase expression in rat brain. Lab Invest 71: 417–422, 1994

    PubMed  Google Scholar 

  20. Maruiwa H, Sasaguri Y, Shigemori M, Hirohata M, Morimatsu M: A role of matrix metalloproteinases produced by glioma cells. Int J Onc 3: 1083–1088, 1993

    Google Scholar 

  21. Nakagawa T, Kubota T, Kabuto M, Sato K, Kawano H, Hayakawa T, Okada Y: Production of matrix metalloproteinases and tissue inhibitor of metalloproteinases-1 by human brain tumors. J Neurosurg 81: 69–77, 1994

    PubMed  Google Scholar 

  22. Rao JS, Steck PA, Mohanam S, Stetler-Stevenson WG, Liotta LA, Sawaya R. Elevated levels of M(r) 92,000 type IV collagenase in human brain tumors. Cancer Res 53: 2208–2211, 1993

    PubMed  Google Scholar 

  23. Yamamoto M, Sawaya R, Mohanam S, et al.: Expression and localization of urokinase-type plasminogen activator in human astrocytomas in vivo. Cancer Res 54: 3656–3661, 1994

    PubMed  Google Scholar 

  24. Rosenberg GA, Dencoff JE, Correa NJ, Reiners M, Ford CC: Effect of steroids on CSF matrix metalloproteinases in multiple sclerosis: relation to blood–brain barrier injury. Neurology 46: 1626–1632, 1996

    PubMed  Google Scholar 

  25. Gijbels K, Masure S, Carton H, Opdenakker G: Gelatinase in the cerebrospinal fluid of patients with multiple sclerosis and other inflammatory neurological disorders. J Neuroimmunol 41: 29–34, 1992

    PubMed  Google Scholar 

  26. Stetler-Stevenson WG, Hewitt R, Corcoran M: Matrix metalloproteinases and tumor invasion: from correlation and causality to the clinic. Semin Cancer Biol 7: 147–154, 1996

    PubMed  Google Scholar 

  27. Sato H, Seiki M: Regulatory mechanism of 92 kDa type IV collagenase gene expression which is associated with invasiveness of tumor cells. Oncogene 8: 395–405, 1993

    PubMed  Google Scholar 

  28. Gottschall PE, Yu X, Bing B: Increased production of gelatinase B (matrix metalloproteinase-9) and interleukin-6 by activated rat microglia in culture. J Neurosci Res 42: 335–342, 1995

    PubMed  Google Scholar 

  29. Kureshi SA, Hofman FM, Schneider JH, Chin LS, Apuzzo MLJ, Hinton DR: Cytokine expression in radiationinduced delayed cerebral injury. Neurosurgery 35: 822–830, 1994

    PubMed  Google Scholar 

  30. D'Avella D, Cicciarello R, Albiero F, et al.: Quantitative study of blood–brain barrier permeability changes after experimental whole-brain radiation. Neurosurgery 30: 30–34, 1992

    PubMed  Google Scholar 

  31. Namba H, Irie T, Fukushi K, Iyo M, Hashimoto T, Ando K: Time courses of changes in cerebral blood flow and blood– brain barrier integrity by focal proton radiation in the rat. Neurol Res 18: 83–86, 1996

    PubMed  Google Scholar 

  32. CammerW, Bloom BR, NortonWT, Gordon S: Degradation of basic protein in myelin by neutral proteases secreted by stimulated macrophages: a possible mechanism of inflammatory demyelination. Proc Natl Acad Sci USA 75: 1554–1558, 1978

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Adair, J.C., Baldwin, N., Kornfeld, M. et al. Radiation-induced Blood–brain Barrier Damage in Astrocytoma: Relation to Elevated Gelatinase B and Urokinase. J Neurooncol 44, 283–289 (1999). https://doi.org/10.1023/A:1006337912345

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1006337912345

Navigation