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Divisions of Neuropathology [D. Z., D. C. M.] and Pediatric Pathology [J. C., M. A. G.], Department of Pathology; Departments of Pharmacology [D. R. F., J. D., M. G.] and Neurology [D. R. F.]; Brain Tumor Research Center [D. Z., D. R. F., D. C. M., M. G.]; the Kaplan Comprehensive Cancer Center [D. Z., D. C. M., M. G., M. A. G.], and the Clinical Research Center and Environmental Medicine [H. C.], New York University Medical Center, New York, New York 10016, and the Department of Pathology and Cell Biology, Thomas Jefferson University, Philadelphia, Pennsylvania 19107 [M. K.]
We investigated the expression and distribution of the extracellular matrix protein tenascin (TN) in 59 astrocytomas and 11 samples of normal brain by Western blot analysis and immunohistochemistry using antibodies against human TN. The tumors included 14 juvenile pilocytic astrocytomas (grade I), 13 low grade fibrillary astrocytomas (grade II), 8 anaplastic astrocytomas (grade III), and 24 glioblastomas multiforme (grade IV). Proliferation indices were calculated by computer-based image analysis after immunostaining with the MIB-1 antibody against the Ki-67 proliferation-associated antigen. Western blot analysis for TN on fresh frozen tumor tissue from 23 of the 59 astrocytomas indicated up to 4-fold higher TN expression in glioblastomas multiforme than in nontumorous control tissues. Enhanced intercellular expression of TN was observed by immunohistochemistry in glioblastomas multiforme. Moreover, TN immunostaining was consistently greater within and around the walls of hyperplastic blood vessels than nonhyperplastic vessels of both high grade tumors and juvenile pilocytic astrocytomas. Juvenile pilocytic astrocytomas with increased TN expression by Western blot analysis had vascular hyperplasia by light microscopy. Proliferation indices moderately correlated with tumor grade. Enhanced immunohistochemical expression of TN was associated with higher tumor grade with higher proliferation indices. The strong association of TN and vascular hyperplasia, regardless of tumor grade, suggests that TN may play a crucial role in angiogenesis.
1 This work was supported in part by NIH Grants (NS 31088 and CA 16087-17), by the Kaplan Comprehensive Cancer Center, and by the Children's Brain Tumor Foundation. Presented in part at the 83rd Annual Meeting of the United States-Canadian Academy of Pathology, March 1218, 1994, San Francisco, CA.
2 To whom requests for reprints should be addressed, at Department of Pathology, Division of Neuropathology, New York University Medical Center, 550 First Avenue, New York, NY 10016.
Received 8/19/94. Accepted 12/14/94.
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