OCT-4 and DAZL expression in precancerous lesions of the human uterine cervix.

J Obstet Gynaecol Res

Laboratory of Stem Cells, Division of Reproductive Medicine, Alexandra Maternity Hospital, Athens, Greece; 1st Department of Obstetrics and Gynecology, Medical School, University of Athens, Athens, Greece.

Published: May 2015

AI Article Synopsis

  • The study aimed to assess the expression of OCT-4 and DAZL in cervical cells affected by HPV and CIN compared to normal cells.
  • OCT-4 was found to be upregulated in HPV-infected cells and showed a trend towards significance in CIN lesions, while DAZL was not expressed in any of the samples.
  • The findings suggest that OCT-4 could be a potential marker for early cervical carcinogenesis, warranting further research into its use for screening and treatment.

Article Abstract

Aim: To determine whether octamer-binding transcription factor 4 (OCT-4) and deleted in azoospermia like (DAZL) are expressed among cells with human papilloma virus (HPV) infection and cervical intraepithelial neoplasia (CIN) lesions and quantify their relative expression when compared with normal cervical cultures.

Methods: Cervical cells derived from normal cell cultures, HPV lesions and CIN lesions were cultured in Dulbecco's modified Eagle's medium supplemented with 20% amniotic fluid and 5 ng/mL basic fibroblast growth factor at 37°C and humidified 10% CO2 in air. Real-time polymerase chain reaction (PCR) was carried out using G6PD as a reference. We used REST for statistical analysis of real-time PCR.

Results: Whereas DAZL was not expressed either in normal cultures or HPV and CIN lesions, OCT-4 was expressed in all examined cell lines. Moreover its relative expression was significantly upregulated among cultures of HPV-infected cells (RE, 11.003; 95%CI: 0.054-36 704.527, P = 0.042), an observation that was also close to statistical significance among cultures of CIN lesions (P = 0.066).

Conclusion: The relative expression of OCT-4 is upregulated during the early, preinvasive stages of cervical carcinogenesis. Future studies should investigate its potential as a screening marker and as a possible target of therapy.

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Source
http://dx.doi.org/10.1111/jog.12640DOI Listing

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