Evaluation of p16 hypermethylation in oral submucous fibrosis: A quantitative and comparative analysis in buccal cells and saliva using real-time methylation-specific polymerase chain reaction
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作者:
Kaliyaperumal, Subadra
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Sri Ramachandra Univ, Fac Dent Sci, Dept Oral Med & Radiol, Madras, Tamil Nadu, IndiaSri Ramachandra Univ, Fac Dent Sci, Dept Oral Med & Radiol, Madras, Tamil Nadu, India
Kaliyaperumal, Subadra
[1
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Sankarapandian, Sathasivasubramanian
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Sri Ramachandra Univ, Fac Dent Sci, Dept Oral Med & Radiol, Madras, Tamil Nadu, IndiaSri Ramachandra Univ, Fac Dent Sci, Dept Oral Med & Radiol, Madras, Tamil Nadu, India
Sankarapandian, Sathasivasubramanian
[1
]
机构:
[1] Sri Ramachandra Univ, Fac Dent Sci, Dept Oral Med & Radiol, Madras, Tamil Nadu, India
Aims: The aim of this study was to quantitatively investigate the hypermethylation of p16 gene in buccal cells and saliva of oral submucous fibrosis (OSMF) patients using real-time quantitative methylation-specific polymerase chain reaction (PCR) and to compare the values of two methods. Subjects and Methods: A total of 120 samples were taken from 60 subjects selected for this study, of which 30 were controls and 30 patients were clinically and histopathologically diagnosed with OSMF. In both groups, two sets of samples were collected, one directly from the buccal cells through cytobrush technique and the other through salivary rinse. We analyzed the samples for the presence of p16 hypermethylation using quantitative real-time PCR. Results: In OSMF, the hypermethylation status of p16 in buccal cells was very high (93.3%) and in salivary samples, it was partially methylated (50%). However, no hypermethylation was found in controls suggesting that significant quantity of p16 hypermethylation was present in buccal cells and saliva in OSMF. Conclusions: This study indicates that buccal cell sampling may be a better method for evaluation than the salivary samples. It signifies that hypermethylation of p16 is an important factor to be considered in epigenetic alterations of normal cells to oral precancer, i.e. OSMF.
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301 Mil Hosp, Chinese PLA Gen Hosp, Urinary, Beijing, Peoples R China301 Mil Hosp, Chinese PLA Gen Hosp, Urinary, Beijing, Peoples R China
Li, H.
Liang, Y.
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Genetron Hlth Beijing Technol Co Ltd, Dept Translat Med, Beijing, Peoples R China301 Mil Hosp, Chinese PLA Gen Hosp, Urinary, Beijing, Peoples R China
Liang, Y.
Ma, T.
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Genetron Hlth Beijing Technol Co Ltd, Dept Translat Med, Beijing, Peoples R China301 Mil Hosp, Chinese PLA Gen Hosp, Urinary, Beijing, Peoples R China
Ma, T.
Ma, X.
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301 Mil Hosp, Chinese PLA Gen Hosp, Urinary, Beijing, Peoples R China301 Mil Hosp, Chinese PLA Gen Hosp, Urinary, Beijing, Peoples R China
Ma, X.
Zheng, Q.
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Genetron Hlth Beijing Technol Co Ltd, Dept R&D, Beijing, Peoples R China301 Mil Hosp, Chinese PLA Gen Hosp, Urinary, Beijing, Peoples R China
Zheng, Q.
Xu, Y.
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301 Mil Hosp, Chinese PLA Gen Hosp, Urinary, Beijing, Peoples R China301 Mil Hosp, Chinese PLA Gen Hosp, Urinary, Beijing, Peoples R China
机构:
Gadjah Mada Univ, Dept Pharmaceut Chem, Sekip Utara 55281, Yogyakarta, IndonesiaGadjah Mada Univ, Dept Pharmaceut Chem, Sekip Utara 55281, Yogyakarta, Indonesia
Kurniasih, Kholif Sholehah, I
Hikmah, Nurull
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Gadjah Mada Univ, Dept Pharmaceut Chem, Sekip Utara 55281, Yogyakarta, IndonesiaGadjah Mada Univ, Dept Pharmaceut Chem, Sekip Utara 55281, Yogyakarta, Indonesia
Hikmah, Nurull
Erwanto, Yuny
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Gadjah Mada Univ, Fac Anim Sci, Div Anim Prod Technol, Jl Fauna 3, Bulaksumur 55281, Yogyakarta, Indonesia
Gadjah Mada Univ, IHIS, Sekip Utara 55281, Yogyakarta, IndonesiaGadjah Mada Univ, Dept Pharmaceut Chem, Sekip Utara 55281, Yogyakarta, Indonesia