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

Authors
Kim, Na RaeChae, Yang SeokLim, Weon JeongCho, Seong Jin
Issue Date
2011
Publisher
KOREAN SOCIETY PATHOLOGISTS
Keywords
Hepatocyte growth factor; c-met; Meningioma; Neoplasm recurrence; local; Reverse transcription polymerase chain reaction
Citation
KOREAN JOURNAL OF PATHOLOGY, v.45, no.5, pp.463 - 468
Indexed
SCIE
SCOPUS
KCI
Journal Title
KOREAN JOURNAL OF PATHOLOGY
Volume
45
Number
5
Start Page
463
End Page
468
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/115037
DOI
10.4132/KoreanJPathol.2011.45.5.463
ISSN
1738-1843
Abstract
Background: 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.
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