Involvement of CELSR3 hypermethylation in primary oral squamous cell carcinoma
Background: Promoter hypermethylation is a frequent epigenetic mechanism for gene transcription repression in cancer and is one of the hallmarks of the disease. Cadherin EGF LAG seven-pass G-type receptor 3 (CELSR3) contributes to cell contact-mediated communication. Dysregulation of promoter methyl...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Asian Pacific Organization for Cancer Prevention
2016
|
Subjects: | |
Online Access: | View Fulltext in Publisher View in Scopus |
LEADER | 03224nam a2200577Ia 4500 | ||
---|---|---|---|
001 | 10.7314-APJCP.2016.17.1.219 | ||
008 | 220120s2016 CNT 000 0 und d | ||
020 | |a 15137368 (ISSN) | ||
245 | 1 | 0 | |a Involvement of CELSR3 hypermethylation in primary oral squamous cell carcinoma |
260 | 0 | |b Asian Pacific Organization for Cancer Prevention |c 2016 | |
520 | 3 | |a Background: Promoter hypermethylation is a frequent epigenetic mechanism for gene transcription repression in cancer and is one of the hallmarks of the disease. Cadherin EGF LAG seven-pass G-type receptor 3 (CELSR3) contributes to cell contact-mediated communication. Dysregulation of promoter methylation has been reported in various cancers. Objectives: The objectives of this study were to investigate the CELSR3 hypermethylation level in oral squamous cell carcinomas (OSCCs) using methylation-sensitive high-resolution melting analysis (MS-HRM) and to correlate CELSR3 methylation with patient demographic and clinicopathological parameters. Materials and Methods: Frozen tissue samples of healthy subjects' normal mucosa and OSCCs were examined with regard to their methylation levels of the CELSR3 gene using MS-HRM. Results: MS-HRM analysis revealed a high methylation level of CELSR3 in 86% of OSCC cases. Significant correlations were found between CELSR3 quantitative methylation levels with patient ethnicity (P=0.005), age (P=0.024) and pathological stages (P=0.004). A moderate positive correlation between CELSR3 and patient age was also evident (R=0.444, P=0.001). Conclusions: CELSR3 promoter hypermethylation may be an important mechanism involved in oral carcinogenesis. It may thus be used as a biomarker in OSCC prognostication. | |
650 | 0 | 4 | |a Biomarker |
650 | 0 | 4 | |a Biomarkers, Tumor |
650 | 0 | 4 | |a cadherin |
650 | 0 | 4 | |a Cadherins |
650 | 0 | 4 | |a Carcinoma, Squamous Cell |
650 | 0 | 4 | |a cell surface receptor |
650 | 0 | 4 | |a CELSR3 |
650 | 0 | 4 | |a Celsr3 protein, human |
650 | 0 | 4 | |a DNA |
650 | 0 | 4 | |a DNA methylation |
650 | 0 | 4 | |a DNA Methylation |
650 | 0 | 4 | |a DNA, Neoplasm |
650 | 0 | 4 | |a female |
650 | 0 | 4 | |a Female |
650 | 0 | 4 | |a gene expression regulation |
650 | 0 | 4 | |a Gene Expression Regulation, Neoplastic |
650 | 0 | 4 | |a genetics |
650 | 0 | 4 | |a human |
650 | 0 | 4 | |a Humans |
650 | 0 | 4 | |a Hypermethylation |
650 | 0 | 4 | |a male |
650 | 0 | 4 | |a Male |
650 | 0 | 4 | |a middle aged |
650 | 0 | 4 | |a Middle Aged |
650 | 0 | 4 | |a Mouth Neoplasms |
650 | 0 | 4 | |a mouth tumor |
650 | 0 | 4 | |a Oral squamous cell carcinoma |
650 | 0 | 4 | |a promoter region |
650 | 0 | 4 | |a Promoter Regions, Genetic |
650 | 0 | 4 | |a Receptors, Cell Surface |
650 | 0 | 4 | |a squamous cell carcinoma |
650 | 0 | 4 | |a tumor marker |
700 | 1 | 0 | |a Abraham, T.M. |e author |
700 | 1 | 0 | |a Froemming, G.R.A. |e author |
700 | 1 | 0 | |a Khor, G.H. |e author |
700 | 1 | 0 | |a Lin, T.K. |e author |
700 | 1 | 0 | |a Zain, R.B. |e author |
773 | |t Asian Pacific Journal of Cancer Prevention |x 15137368 (ISSN) |g 17 1, 219-223 | ||
856 | |z View Fulltext in Publisher |u https://doi.org/10.7314/APJCP.2016.17.1.219 | ||
856 | |z View in Scopus |u https://www.scopus.com/inward/record.uri?eid=2-s2.0-84957976334&doi=10.7314%2fAPJCP.2016.17.1.219&partnerID=40&md5=1cc023df70045e5f0d584c1349df8bdd |