Your browser doesn't support javascript.
loading
Relative Expression of OCT4, SOX2 and NANOG in Oral Squamous Cell Carcinoma Versus Adjacent Non- Tumor Tissue.
Baghai Naini, Fereshteh; Aminishakib, Pouyan; Abdollahi, Alireza; Hodjat, Mahshid; Mohammadpour, Hadiseh; Kardouni Khoozestani, Neda.
Afiliação
  • Baghai Naini F; Department of Oral and Maxillofacial Pathology, Faculty of Dentistry, Tehran University of Medical Science, Tehran, Iran. Email: nkardouni@sina.tums.ac.ir
  • Aminishakib P; Dental Research Center, Dentistry Research Institute,Tehran University of Medical Sciences, Tehran, Iran.
  • Abdollahi A; Department of Oral and Maxillofacial Pathology, Faculty of Dentistry, Tehran University of Medical Science, Tehran, Iran. Email: nkardouni@sina.tums.ac.ir
  • Hodjat M; Department of Pathology, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.
  • Mohammadpour H; Dental Research Center, Dentistry Research Institute,Tehran University of Medical Sciences, Tehran, Iran.
  • Kardouni Khoozestani N; Iran National Tumor Bank, Cancer Institute, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.
Asian Pac J Cancer Prev ; 20(6): 1649-1654, 2019 06 01.
Article em En | MEDLINE | ID: mdl-31244283
ABSTRACT

Objective:

Oral squamous cell carcinoma (OSCC) accounts for over 90% of oral neoplasms. Finding molecular markers for predicting prognosis is a high priority. The core transcription factors, OCT4, SOX2, and NANOG that regulate embryonic stem cell pluripotency have been implicated in progression of various malignancies. The predictive value of these markers and their role in the development of OSCC is still controversial. In this study, we therefore evaluated their expression in OSCCs and adjacent non-tumor tissue.

Methods:

A total of 60 frozen tumor and adjacent non-tumor tissue samples from 30 patients with OSCC were examined using quantitative reverse transcription polymerase chain reaction (qRT-PCR). Clinical and pathological data of patients including tumor stage, lymph node metastasis and tumor grade were also recorded.

Results:

Expression of SOX2 was significantly higher in adjacent non-tumor as compared to tumor tissue (P=0.04). No statistically significant differences were found for expression of OCT4 (P=0.50) and NANOG (P=0.68). Also, there was no significant association between expression of OCT4, SOX2, and NANOG and clinical or pathological data (P>0.05), although slightly higher values were noted in patients without lymph node metastasis.

Conclusion:

Based on the present data, decreased expression of SOX2 is correlated with carcinogenesis in the oral cavity and development of OSCC.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Bucais / Carcinoma de Células Escamosas / Biomarcadores Tumorais / Fator 3 de Transcrição de Octâmero / Fatores de Transcrição SOXB1 / Proteína Homeobox Nanog Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Bucais / Carcinoma de Células Escamosas / Biomarcadores Tumorais / Fator 3 de Transcrição de Octâmero / Fatores de Transcrição SOXB1 / Proteína Homeobox Nanog Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article