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Expression of Hepatocyte Growth Factor/c-met by RT-PCR in Meningiomas

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dc.contributor.authorKim, Na Rae-
dc.contributor.authorChae, Yang Seok-
dc.contributor.authorLim, Weon Jeong-
dc.contributor.authorCho, Seong Jin-
dc.date.accessioned2021-09-07T21:55:10Z-
dc.date.available2021-09-07T21:55:10Z-
dc.date.created2021-06-14-
dc.date.issued2011-
dc.identifier.issn1738-1843-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/115037-
dc.description.abstractBackground: Hepatocyte growth factor (HGF) is a potent mitogenic cytokine. C-met protein, which is known to be the HGF receptor has transmembrane tyrosine kinase activity and is encoded by the c-met oncogene. The HGF/c-met signaling pathway may play various roles in the carcinogenesis of various organs. Methods: We examined HGF and c-met mRNA expression by utilizing reverse transcription polymerase chain reaction on 40 surgically resected intracranial meningiomas (25 benign, 10 atypical, and 5 anaplastic cases). Results: An HGF overexpression was detected in 28%, 50%, and 80% of the benign, atypical and anaplastic meningiomas, respectively; a high expression of HGF or the coexpression of HGF/c-met was detected in the high grade meningiomas (the atypical and anaplastic cases, p = 0.046, p = 0.014). An HGF expression was statistically significant in the recurrent meningiomas (p = 0.003), and HGF expression was significantly lower than c-met mRNA expression in benign meningiomas (p = 0.034). Conclusions: There was no correlation between histologic subtypes and HGF/c-met expression. Determination of HGF expression can be used as a molecular predictor for recurrence of meningioimas. These results suggest that HGF and c-met expression in meningiomas may be associated with anaplastic progression.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherKOREAN SOCIETY PATHOLOGISTS-
dc.subjectFACTOR SCATTER FACTOR-
dc.subjectFACTOR/SCATTER FACTOR HGF/SF-
dc.subjectRECEPTOR C-MET-
dc.subjectPREDICT RECURRENCE-
dc.subjectOVEREXPRESSION-
dc.subjectMOTILITY-
dc.subjectGLIOMAS-
dc.subjectBENIGN-
dc.subjectPOTENT-
dc.subjectMIB-1-
dc.titleExpression of Hepatocyte Growth Factor/c-met by RT-PCR in Meningiomas-
dc.typeArticle-
dc.contributor.affiliatedAuthorChae, Yang Seok-
dc.identifier.doi10.4132/KoreanJPathol.2011.45.5.463-
dc.identifier.scopusid2-s2.0-84856655644-
dc.identifier.wosid000297157100003-
dc.identifier.bibliographicCitationKOREAN JOURNAL OF PATHOLOGY, v.45, no.5, pp.463 - 468-
dc.relation.isPartOfKOREAN JOURNAL OF PATHOLOGY-
dc.citation.titleKOREAN JOURNAL OF PATHOLOGY-
dc.citation.volume45-
dc.citation.number5-
dc.citation.startPage463-
dc.citation.endPage468-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART001596681-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaPathology-
dc.relation.journalWebOfScienceCategoryPathology-
dc.subject.keywordPlusFACTOR SCATTER FACTOR-
dc.subject.keywordPlusFACTOR/SCATTER FACTOR HGF/SF-
dc.subject.keywordPlusRECEPTOR C-MET-
dc.subject.keywordPlusPREDICT RECURRENCE-
dc.subject.keywordPlusOVEREXPRESSION-
dc.subject.keywordPlusMOTILITY-
dc.subject.keywordPlusGLIOMAS-
dc.subject.keywordPlusBENIGN-
dc.subject.keywordPlusPOTENT-
dc.subject.keywordPlusMIB-1-
dc.subject.keywordAuthorHepatocyte growth factor-
dc.subject.keywordAuthorc-met-
dc.subject.keywordAuthorMeningioma-
dc.subject.keywordAuthorNeoplasm recurrence-
dc.subject.keywordAuthorlocal-
dc.subject.keywordAuthorReverse transcription polymerase chain reaction-
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