RESUMEN
Background and Objectives: PIN1 is overexpressed in several human cancers, including prostate cancer, breast cancer, and oral squamous carcinomas. Juglone (J), derived from walnut, was reported to selectively inhibit PIN1 by modifying its sulfhydryl groups. In this study, the potential effects of juglone, also known as PIN1 inhibitor, on oral cancer and carcinogenesis were investigated at the molecular level. Materials and Methods: 4-Nitroquinoline N-oxide (4-NQO) was used to create an oral cancer model in animals. Wistar rats were divided into five groups: Control, NQO, Juglone, NQO+J, and NQO+J*. The control group received the basal diet and tap water throughout the experiment. The NQO group received 4-NQO for 8 weeks in drinking water only. The Juglone group was administered intraperitoneally in a juglone solution for 10 weeks (1 mg/kg/day). The NQO+J group received 4-NQO in drinking water for 8 weeks, starting 1 week after the cessation of 4-NQO treatment. They were then administered intraperitoneally in a juglone solution for 10 weeks. (1 mg/kg/day). NQO+J* group: received 4 NQO for 8 weeks in drinking water and administered intraperitoneally in a juglone solution for 10 weeks (1 mg/kg/day). They were sacrificed at the end of the 22-week experimental period. The tongue tissues of the rats were isolated after the experiment, morphological changes were investigated by histological examinations, and the molecular apoptotic process was investigated by rt-qPCR and western blot. Results: Histological results indicate that tumors are formed in the tongue tissue with 4-NQO, and juglone treatment largely corrects the epithelial changes that developed with 4-NQO. It has been determined that apoptotic factors p53, Bax, and caspases are induced by the effect of juglone, while antiapoptotic factors such as Bcl-2 are suppressed. However, it was observed that the positive effects were more pronounced in rats given juglone together with 4-NQO. Conclusions: The use of PIN1 inhibitors such as juglone in place of existing therapeutic approaches might be a promising and novel approach to the preservation and treatment of oral cancer and carcinogenesis. However, further research is required to investigate the practical application of such inhibitors.
Asunto(s)
4-Nitroquinolina-1-Óxido , Modelos Animales de Enfermedad , Neoplasias de la Boca , Naftoquinonas , Ratas Wistar , Animales , Naftoquinonas/farmacología , Naftoquinonas/uso terapéutico , 4-Nitroquinolina-1-Óxido/toxicidad , Ratas , Neoplasias de la Boca/inducido químicamente , Neoplasias de la Boca/patología , Masculino , Peptidilprolil Isomerasa de Interacción con NIMA/metabolismo , Apoptosis/efectos de los fármacos , Carcinogénesis/efectos de los fármacosRESUMEN
BACKGROUND: Persistent primary teeth (PPT) may occur due to various local factors, or it may develop due to general factors such as systemic diseases and syndromes. Since eruption and dental development are two different processes, it is important to investigate both processes to determine the actual cause of delayed tooth eruption. The study aimed to evaluate the dental development of a group of Turkish children with multiple PPT using the Willems dental age estimation method. STUDY DESIGN: Digital panoramic radiographs of children and adolescents aged between 9 and 15 years were retrieved, assessed and categorized. A total of 80 radiographs of patients with more than one PPT were selected and matched with children without PPT. Dental age was calculated using the method of Willems et al. All analyses were conducted using the SPSS statistical software. The statistical significance was set at 0.05. RESULTS: The permanent tooth development of children with multiple PPT could be delayed by 0.5-4 years compared to healthy ones. A strong positive correlation was found between the number of PPT and deviation for both females and males (p < 0.001). CONCLUSION: In conclusion, we found that permanent tooth development of children with multiple PPT could be delayed compared to healthy ones. In addition, as the number of PPT increased, the difference between chronological age and dental age also increased, especially in males.