Publication:
Tenascin in meningioma: Expression is correlated with anaplasia, vascular endothelial growth factor expression, and peritumoral edema but not with tumor border shape

dc.contributor.authorsKilic, T; Bayri, Y; Ozduman, K; Acar, M; Diren, S; Kurtkaya, O; Ekinci, G; Bugra, K; Sav, A; Ozek, MM; Pamir, MN
dc.date.accessioned2022-03-12T17:00:44Z
dc.date.accessioned2026-01-10T16:54:01Z
dc.date.available2022-03-12T17:00:44Z
dc.date.issued2002
dc.description.abstractOBJECTIVE: Tenascin is an extracellular matrix glycoprotein that is expressed-during embryogenesis, inflammation, angiogenesis, and carcinogenesis. The aim of this study was to investigate how tenascin expression relates to histological grade, angiogenesis, and radiological finding's in meningiomas. METHODS: Twenty typical, atypical, and 5 malignant meningiomas were studied retrospectively. Tenascin expression and vascular endothelial growth factor (VEGF) expression in the tumor tissue were, investigated by immunohistochemistry. tenascin messenger ribonucleic acid expression, was, also studied by comparative reverse transcriptase-polymerase chain reaction. Magnetic resonance images from each case were assessed, for peritumoral edema and tumor border shape. RESULTS: the atypical and malignant meningiomas showed higher levels of tenascin expression than the typical meningiomas. The more sensitive messenger ribonucleic acid-based methods confirmed. this, finding. Tenascin expression was correlated with peritumoral edema and VEGF expression but not with tumor border shape. In the 13 tumors with marked tenascin expression, edema was Grade 0 in one, Grade 1 in three, and Grade 2 in nine specimens. In the same 13 tumors, VEGF expression was Grade 1 in five and Grade 2 in eight specimens, and the findings,for tumor border shape were Grade 0 in Seven, Grade 1 in four, and Grade 2 in two specimens. CONCLUSION: In meningiomas tenascin expression is correlated with anaplasia, tumor-associated edema, and VEGF expression but not with tumor border shape. This protein may play a role in the neoplastic and/or angiogenic processes in atypical and malignant meningiomas and may thus be a potential target for meningioma therapy.
dc.identifier.doi10.1227/01.NEU.0000017466.25827.18
dc.identifier.eissn1524-4040
dc.identifier.issn0148-396X
dc.identifier.pubmed12182416
dc.identifier.urihttps://hdl.handle.net/11424/227333
dc.identifier.wosWOS:000176611700039
dc.language.isoeng
dc.publisherOXFORD UNIV PRESS INC
dc.relation.ispartofNEUROSURGERY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectangiogenesis
dc.subjectextracellular matrix
dc.subjectmeningioma
dc.subjectperitumoral edema
dc.subjecttenascin
dc.subjectHUMAN BRAIN-TUMORS
dc.subjectGLIOMA CELL-LINES
dc.subjectEXTRACELLULAR-MATRIX
dc.subjectFACTOR RECEPTORS
dc.subjectMALIGNANT GLIOMAS
dc.subjectC EXPRESSION
dc.subjectIN-VITRO
dc.subjectINTRACRANIAL MENINGIOMAS
dc.subjectHUMAN ASTROCYTOMAS
dc.subjectMOLECULAR-BIOLOGY
dc.titleTenascin in meningioma: Expression is correlated with anaplasia, vascular endothelial growth factor expression, and peritumoral edema but not with tumor border shape
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage192
oaire.citation.issue1
oaire.citation.startPage183
oaire.citation.titleNEUROSURGERY
oaire.citation.volume51

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