Your browser doesn't support javascript.
loading
Retrospective case-control study of correlation between MTHFR gene and OSCC risk in North India.
Naqvi, Hena; Ahmad, Mohammad Kaleem; Hussain, Syed Rizwan; Gupta, Shalini; Waseem, Mohammad; Mahdi, Abbas Ali.
Afiliación
  • Naqvi H; Molecular Cell Biology Lab, Department of Biochemistry, King George's Medical University, Lucknow, Uttar Pradesh, 226 003, India.
  • Ahmad MK; Molecular Cell Biology Lab, Department of Biochemistry, King George's Medical University, Lucknow, Uttar Pradesh, 226 003, India. kaleembaksh@gmail.com.
  • Hussain SR; Molecular Cell Biology Lab, Department of Biochemistry, King George's Medical University, Lucknow, Uttar Pradesh, 226 003, India.
  • Gupta S; Department of Oral Pathology & Microbiology, King George's Medical University, Lucknow, Uttar Pradesh, 226 003, India.
  • Waseem M; Molecular Cell Biology Lab, Department of Biochemistry, King George's Medical University, Lucknow, Uttar Pradesh, 226 003, India.
  • Mahdi AA; Molecular Cell Biology Lab, Department of Biochemistry, King George's Medical University, Lucknow, Uttar Pradesh, 226 003, India.
Clin Oral Investig ; 21(6): 1929-1934, 2017 Jul.
Article en En | MEDLINE | ID: mdl-27774577
BACKGROUND: Oral squamous cell carcinoma (OSCC) occurrence appears to be the number one among all cancers in India. Folate is a methyl donor during DNA methylation, as it provides substrate for methylenetetrahydrofolate reductase (MTHFR) to convert 5,10-MTHF to 5-MTHF and subsequently metabolizes it to methionine. The purpose of this study was to identify MTHFR C677T gene polymorphism in patients with OSCC. MATERIALS AND METHODS: A total of 350 OSCC cases and 350 healthy controls participated in this study. MTHFR C677T single-nucleotide polymorphism was evaluated by PCR-RFLP. RESULTS: In the present study, MTHFR gene 677CC, CT, and TT genotype frequencies of the total OSCC cases were 74.8; 19.4 and 5.71; and 88.5, 9.42, and 2.0 % in controls. The average frequency of the MTHFR 677T allele was 15.4 % in OSCC cases compared to 6.71 % in the controls. The CT genotype occurrence prevailed more in patients than controls in contrast to TT genotype, although both the genotypes were statistically significant for OSCC. Moreover, we found that T allele was significant in cases of smoking and tobacco chewing. CONCLUSIONS: In this study, we found that the homozygous mutant T allele appeared to have significantly higher risk of OSCC especially in late stages and therefore supporting in OSCC susceptibility and its progression.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Boca / Carcinoma de Células Escamosas / Polimorfismo de Nucleótido Simple / Metilenotetrahidrofolato Reductasa (NADPH2) Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Clin Oral Investig Asunto de la revista: ODONTOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: India

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Boca / Carcinoma de Células Escamosas / Polimorfismo de Nucleótido Simple / Metilenotetrahidrofolato Reductasa (NADPH2) Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Clin Oral Investig Asunto de la revista: ODONTOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: India