TY - JOUR
T1 - An altered keratinocyte phenotype in oral submucous fibrosis
T2 - Correlation of keratin K17 expression with disease severity
AU - Lalli, Anand
AU - Tilakaratne, Wanninayake M.
AU - Ariyawardana, Anura
AU - Fitchett, Caroline
AU - Leigh, Irene M.
AU - Hagi-Pavli, Eleni
AU - Cruchley, Alan T.
AU - Parkinson, E.Kenneth
AU - Teh, Muy-Teck
AU - Fortune, Farida
AU - Waseem, Ahmad
N1 - MEDLINE® is the source for the MeSH terms of this document.
PY - 2008
Y1 - 2008
N2 - Oral submucous fibrosis (OSF) is characterized by abnormal collagen metabolism in the submucosal connective tissue. Its influence on the overlying epithelium is not known but about 14% of OSF cases undergo malignant transformation to squamous cell carcinoma indicating association with abnormality of the epithelium. Here, we have defined the keratin expression profile, by immunohistochemistry and quantitative image analysis, using a panel of 22 anti-keratin monoclonal antibodies on 28 OSF samples. We observed an increase of K1 and K10 in the suprabasal layers, induction of K6 in the basal layer and complete loss of K19 in the epithelium. Furthermore, there was increased K17 expression in the suprabasal layers, which correlated with disease severity. In a subset of the most severe OSF cases (14%), K17 expression was completely lost in the basal layer which might define them to be at most risk to undergo malignant transformation. There was no detectable expression of K8, K18, K7 and K9 and the expression of K4, K13, K14, K15 and K16 did not change in OSF. We propose that the altered keratin profiles could be useful as histological diagnostic markers and provide important insights into the pathogenesis of the disease and its predisposition to malignancy.
AB - Oral submucous fibrosis (OSF) is characterized by abnormal collagen metabolism in the submucosal connective tissue. Its influence on the overlying epithelium is not known but about 14% of OSF cases undergo malignant transformation to squamous cell carcinoma indicating association with abnormality of the epithelium. Here, we have defined the keratin expression profile, by immunohistochemistry and quantitative image analysis, using a panel of 22 anti-keratin monoclonal antibodies on 28 OSF samples. We observed an increase of K1 and K10 in the suprabasal layers, induction of K6 in the basal layer and complete loss of K19 in the epithelium. Furthermore, there was increased K17 expression in the suprabasal layers, which correlated with disease severity. In a subset of the most severe OSF cases (14%), K17 expression was completely lost in the basal layer which might define them to be at most risk to undergo malignant transformation. There was no detectable expression of K8, K18, K7 and K9 and the expression of K4, K13, K14, K15 and K16 did not change in OSF. We propose that the altered keratin profiles could be useful as histological diagnostic markers and provide important insights into the pathogenesis of the disease and its predisposition to malignancy.
UR - http://www.scopus.com/inward/record.url?scp=40449137031&partnerID=8YFLogxK
U2 - 10.1111/j.1600-0714.2007.00609.x
DO - 10.1111/j.1600-0714.2007.00609.x
M3 - Article
AN - SCOPUS:40449137031
SN - 0904-2512
VL - 37
SP - 211
EP - 220
JO - Journal of Oral Pathology and Medicine
JF - Journal of Oral Pathology and Medicine
IS - 4
ER -