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1.
Arch Oral Biol ; 110: 104627, 2020 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-31862643

RESUMEN

OBJECTIVE: To evaluate the immunoexpression of DNA base excision repair (BER) [apurinic/apyrimidinic endonuclease 1 (APE-1), X-ray repair cross complementing 1 (XRCC-1)] and nucleotide excision repair (NER) [xeroderma pigmentosum complementation group (XPF)] proteins in benign epithelial odontogenic lesions with different biological behaviors. DESIGN: Thirty solid ameloblastomas, 30 non-syndromic odontogenic keratocysts (NSOKCs), 29 syndromic odontogenic keratocysts (SKOCs), 30 dentigerous cysts (DCs) and 20 dental follicles (DFs) were evaluated quantitatively for APE-1, XRCC-1 and XPF through immunohistochemistry. RESULTS: Nuclear expression of APE-1 was significantly higher in NSOKCs, SOKCs, and ameloblastomas in comparison to DCs (p < 0.001). Nuclear expression of XRCC-1 was higher in NSOKCs and SOKCs than in DCs (p < 0.05). At the nuclear level, XPF expression was higher in NSOKCs and SOKCs than in DCs and ameloblastomas (p < 0.05). A statistically significant higher expression of APE-1 (nuclear), XRCC-1 (nuclear), and XPF (nuclear and cytoplasmic) was found in all odontogenic lesion samples as compared to DFs (p < 0.05). For all lesions, there was a positive correlation between nuclear expression of APE-1 and XRCC-1 or XPF (p < 0.05). CONCLUSIONS: Our results suggest a potential involvement of APE-1, XRCC-1 and XPF proteins in the pathogenesis of benign epithelial odontogenic lesions, especially in those with more aggressive biological behavior, such as ameloblastomas, NSOKCs, and SOKCs. We also showed that the expression of APE-1 was positively correlated with the nuclear expression of XRCC-1 and XPF, which may suggest an interaction between the BER and NER pathways in all odontogenic lesions studied herein.


Asunto(s)
Ameloblastoma , Reparación del ADN , ADN-(Sitio Apurínico o Apirimidínico) Liasa , Proteínas de Unión al ADN , Quiste Dentígero , Quistes Odontogénicos , Proteína 1 de Reparación por Escisión del Grupo de Complementación Cruzada de las Lesiones por Rayos X , Ameloblastoma/genética , ADN , ADN-(Sitio Apurínico o Apirimidínico) Liasa/metabolismo , Proteínas de Unión al ADN/metabolismo , Quiste Dentígero/genética , Expresión Génica , Humanos , Quistes Odontogénicos/genética , Proteína 1 de Reparación por Escisión del Grupo de Complementación Cruzada de las Lesiones por Rayos X/metabolismo
2.
Arch Oral Biol ; 56(11): 1256-63, 2011 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-21683340

RESUMEN

OBJECTIVE: Receptor activator of nuclear factor-κB (RANK), RANK ligand (RANKL) and osteoprotegerin (OPG) are members of the superfamily of ligands and receptors of tumour necrosis factor family involved in bone metabolism. The formation, differentiation and activity of osteoclasts are regulated by these proteins. To clarify the roles of osteoclast regulatory factors in cystic expansion of odontogenic cysts, expression of these proteins were analysed in radicular and dentigerous cysts. DESIGN: The immunohistochemistry expression of these biomarkers were evaluated and measured in lining epithelium and fibrous capsule of the radicular (n=20) and dentigerous cysts (n=20). RESULTS: A similar expression in lining epithelium was observed in the lesions. The fibrous capsule of dentigerous cyst showed a higher content of RANK-positive and RANKL-positive cells than fibrous capsule of radicular cyst. In the lining epithelium the RANKL/OPG ratio showed higher numbers of OPG-positive than RANKL-positive cells, whereas fibrous capsule of the cysts had a tendency to present a similar expression (OPG=RANKL). CONCLUSION: Ours findings indicate the presence of RANK, RANKL and OPG in cysts. Moreover, increased expression of OPG compared to RANKL in the lining epithelium could contribute to the differential bone resorption activity in theses lesions.


Asunto(s)
Quiste Dentígero/metabolismo , Enfermedades Mandibulares/metabolismo , Enfermedades Maxilares/metabolismo , Osteoprotegerina/biosíntesis , Ligando RANK/biosíntesis , Quiste Radicular/metabolismo , Receptor Activador del Factor Nuclear kappa-B/biosíntesis , Adolescente , Adulto , Niño , Quiste Dentígero/genética , Epitelio/metabolismo , Femenino , Humanos , Inmunohistoquímica , Masculino , Enfermedades Mandibulares/genética , Enfermedades Maxilares/genética , Persona de Mediana Edad , Osteoclastos/metabolismo , Quiste Radicular/genética , Adulto Joven
3.
J Craniofac Surg ; 20(6): 2036-40, 2009 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-19881373

RESUMEN

Cysts are considered as nonneoplastic benign lesions that, when present for a long period of time, can cause some discomfort, especially related to the treatment form. Among the types of cysts of the maxilla, the dentigerous cyst (DC) presents substances between the dental follicle and the crown of the tooth with high potential for resorption, and the odontogenic keratocyst tumor (OKT) characterizes for its noticed rapid growth pattern and the possibility to develop carcinomas in the lesion wall. The DC is the most common type among the developing odontogenic cystic lesions, while the OKT represents 10% of these lesions. The prevalence of the OKT found in the current study was superior to the DC, opposing data of the evaluated literature, as well as the predominance in relation to the age group. Dentigerous cyst cases were found mostly in younger individuals, whereas the OKT was observed mainly in individuals between the third and fourth decades of life. This fact reflects the fragility of these features while establishing the presumptive diagnosis and insinuates the strong relation with a probable genetic predisposition. In relation to sex and race, the findings in this article were similar to those found in the literature, highlighting the possibility of a hormonal involvement. However, the anatomopathologic examination remains essential to define the main diagnosis of the lesions observed by means of imaging examinations, providing for safer diagnoses to plan the treatment.


Asunto(s)
Quiste Dentígero/epidemiología , Neoplasias Maxilomandibulares/epidemiología , Tumores Odontogénicos/epidemiología , Adolescente , Adulto , Edad de Inicio , Anciano , Brasil/epidemiología , Transformación Celular Neoplásica , Niño , Quiste Dentígero/complicaciones , Quiste Dentígero/genética , Femenino , Predisposición Genética a la Enfermedad , Humanos , Incidencia , Neoplasias Maxilomandibulares/complicaciones , Neoplasias Maxilomandibulares/genética , Masculino , Persona de Mediana Edad , Tumores Odontogénicos/complicaciones , Tumores Odontogénicos/genética , Prevalencia , Estudios Retrospectivos , Razón de Masculinidad , Diente Impactado/etiología , Adulto Joven
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