Please use this identifier to cite or link to this item: https://repository.unej.ac.id/xmlui/handle/123456789/106573
Title: Enhanced Expression of Podoplanin in Oral Carcinomas in situ and Squamous Cell Carcinomas
Authors: FUNAYAMA, Akinori
CHENG, Jun
MARUYAMA, Satoshi
YAMAZAKI, Manabu
KOBAYASHI, Takanori
SYAFRIADI, Mei
KUNDU, Sukalyan
SHINGAKI, Susumu
SAITO, Chikara
SAKU, Takashi
Keywords: CARCINOMA IN SITU
D2-40
EPHITELIAL DYSPLASIA
ORAL MUCOSA
PODOPLANIN
SQUAMOUS CELL CARCINOMA
Issue Date: 8-Feb-2011
Publisher: Pathobiology
Abstract: Objective: Podoplanin, a known lymphatic endothelial cell marker, has been reported to be expressed in various types of cancer. To elucidate the expression of podoplanin in precancerous lesions, we examined the immunohistochemical profiles of podoplanin in oral squamous epithelial lesions. Method: We studied a total of 298 foci of squamous cell carcinoma (SCC), carcinoma in situ (CIS), epithelial dysplasia, and hyperplastic and/or normal epithelial lesions by immunohistochemistry using D2-40. Results: There was no positivity for podoplanin in normal or hyperplastic epithelia, while all of the CIS and SCC foci stained positive. Approximately one third of the mild dysplasia foci (10 of 36 foci, 28%) and 80% of moderate dysplasia foci (78/98) showed grade 1 positive reactions (positive only in the 1st layer). Grade 2 reactions (up to 4th layer) were seen in 4 of 98 moderate dysplasia foci (4%), 29 of 74 CIS foci (39%), and 3 of 30 SCC foci (10%). Grade 3 reactions (to more than 5th layer) were found in 35 (47%) CIS foci and 26 (87%) SCC foci. Conclusions: The relationship between the present histological categorization and podoplanin grade was statistically significant. D2- 40 expression is considered to be related to the severity of oral precancerous lesions.
Gov't Doc #: Kodeprodi#1610101#KedokteranGigi
0029056802
URI: http://repository.unej.ac.id/xmlui/handle/123456789/106573
Appears in Collections:LSP-Jurnal Ilmiah Dosen



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.