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1.
Front Immunol ; 14: 1128352, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37090737

RESUMO

Introduction: People with hazardous alcohol use are more susceptible to viral, bacterial, and fungal infections due to the effect of alcohol on immune system cell function. Metabolized ethanol reduces NAD+ to NADH, affecting critical metabolic pathways. Here, our aim was to investigate whether alcohol is metabolized by bone marrow cells and if it impacts the metabolic pathways of leukocyte progenitor cells. This is said to lead to a qualitative and quantitative alteration of key metabolites which may be related to the immune response. Methods: We addressed this aim by using C57BL/6 mice under chronic ethanol administration and evaluating the metabolomic profile of bone marrow total cells by gas chromatography-coupled mass spectrometry (GC-MS). Results: We identified 19 metabolites. Our data demonstrated that chronic ethanol administration alters the metabolomic profile in the bone marrow, resulting in a statistically diminished abundance of five metabolites in ethanol-treated animals: uracil, succinate, proline, nicotinamide, and tyrosine. Discussion: Our results demonstrate for the first time in the literature the effects of alcohol consumption on the metabolome content of hematopoietic tissue and open a wide range of further studies to investigate mechanisms by which alcohol compromises the cellular function of the immune system.


Assuntos
Medula Óssea , Etanol , Camundongos , Animais , Camundongos Endogâmicos C57BL , Etanol/farmacologia , Metabolômica/métodos , Metaboloma
2.
Med. oral patol. oral cir. bucal (Internet) ; 26(3): e292-e298, May. 2021. tab, ilus
Artigo em Inglês | IBECS | ID: ibc-224506

RESUMO

Background: Among the oral potentially malignant disorders, leukoplakia stands out as the most prevalent. Thepurpose of this study was to analyse the clinical-pathological features of oral leukoplakia in groups of patientsfrom three major pathology centers in two different regions of Brazil, in order to determine which factors wouldbe associated to the clinical risk of malignant transformation.Material and Methods: A total of 148 patients was analyzed, and data regarding gender, age, site, classification ofthe clinical subtype, harmful habits such as use of tobacco and alcohol, time of evolution and presence of dyspla-sia were collected. The association between risk factors and malignant transformation was investigated using thechi-square test and Fischer's exact test for correlation of variables. A significance level of 5% (p≤0.05) was used.Results: The mean age of the patients was 60 years, and 56% were female. Most of the lesions (34,5%) were lo-cated in the lateral and ventral regions of the tongue. Of the 148 patients, ninety had clinical follow-up. Malignanttransformation occurred in 13 patients (8.8%), with an average of 44 months of follow up.Conclusions: Non-smoker, nonhomogeneous clinical presentation, location at the tongue, and the presence of highdegree of dysplasia were statistically relevant factors associated with a higher risk of transformation transformation.(AU)


Assuntos
Humanos , Masculino , Feminino , Leucoplasia Oral/complicações , Leucoplasia Oral/diagnóstico , Leucoplasia Oral/patologia , Carcinoma de Células Escamosas , Estudos Retrospectivos , Brasil , Saúde Bucal , Patologia Bucal , Medicina Bucal , Cirurgia Bucal , Fatores de Risco
3.
J Periodontal Res ; 55(3): 426-431, 2020 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-31943216

RESUMO

BACKGROUND AND OBJECTIVE: Epigenetic events, as the DNA methylation, may be related to development of inflammatory diseases. Due to the important role of host's response in the pathogenesis of periodontitis, the purpose of the present study was to investigate the methylation profile of genes related to immune response in gingival tissues from patients with generalized periodontitis (GP) compared to healthy individuals. METHODS: Gingival tissues were collected from 20 individuals with GP and 20 healthy individuals. Genomic DNA was extracted and submitted to enzymatic digestions. An initial screening using a panel of genes involved with the response immune was performed in pools containing six samples of each group. Genes that presented different levels of methylation between the groups were selected for individual assays for validation. RESULTS: The array results showed an unmethylated profile in the majority of genes evaluated in both groups. MALT1, LTB, and STAT5 genes presented a profile of partial methylation in the control compared with GP group. Validation individual assays using a larger number of samples (n = 20, each group) confirmed the hypomethylation of STAT5 in the GP group compared with control group (P < .001). CONCLUSION: Generalized periodontitis is associated with hypomethylation of the STAT5 gene. Further studies are necessary to evaluate the functional impact these findings.


Assuntos
Metilação de DNA , Periodontite/genética , Periodontite/imunologia , Fator de Transcrição STAT5/genética , Estudos de Casos e Controles , Gengiva , Humanos , Regiões Promotoras Genéticas
4.
Artigo em Inglês | MEDLINE | ID: mdl-29472118

RESUMO

OBJECTIVES: The odontogenic keratocyst (OKC) is an aggressive odontogenic cyst that has a high recurrence rate. Apart from PTCH1 mutations, few molecular alterations are described in OKCs. Low expression of microRNAs (miRNAs) miR-15a and/or miR-16-1 in association with increased expression of their target, Bcl-2, have been previously found in OKC. In humans, MIR15A and MIR16-1 are clustered at chromosome position 13 q14, and loss of heterozygosity (LOH) at this locus occurs in different tumors. We aimed to determine whether deletion at 13 q14 is a potential mechanism leading to miR-15a/16-1 aberrant expression in OKC. METHODS: Genomic DNA was extracted from 15 formalin-fixed, paraffin-embedded microdissected OKC cases. The polymorphic DNA markers D13S272 and D13S273 on chromosome 13 q14.3, around MIR15A/MIR16-1, were amplified by polymerase chain reaction. LOH was examined by capillary electrophoresis DNA-fragment analysis. RESULTS: The D13S272 marker had no LOH in 12 informative cases, whereas 2 out of 9 informative cases (22%) had LOH at the D13S273 marker. CONCLUSIONS: An LOH event at MIR15A/MIR16-1 locus is not common in OKC. The mechanism underlying the regulation of miR-15a and miR-16-1 expression in OKC remains to be determined.


Assuntos
Perda de Heterozigosidade , MicroRNAs/genética , Cistos Odontogênicos/genética , Tumores Odontogênicos/genética , Proteínas Proto-Oncogênicas c-bcl-2/genética , Adolescente , Adulto , Cromossomos Humanos Par 13 , Fragmentação do DNA , Eletroforese Capilar , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Cistos Odontogênicos/patologia , Tumores Odontogênicos/patologia , Reação em Cadeia da Polimerase
5.
Pathobiology ; 79(1): 18-23, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22236544

RESUMO

OBJECTIVE: To investigate the DNMT3B (C46359T) polymorphism and immunoexpression of DNMT3b and DNMT1 in oral lichen planus (OLP) compared to a control group. METHODS: We aimed to investigate the DNMT3B (C46359T) polymorphism and immunoexpression of DNMT3b and DNMT1 in OLP (n = 32), comparing it with oral mucosa (control; n = 24). The DNMT3B (C46359T) polymorphism was analyzed using the RFLP-PCR and DNMT1, and DNMT3a proteins were identified using immunohistochemistry. We also compared the DNMT3B expression in OLP and oral inflammatory fibrous hyperplasia (OIFH), another oral inflammatory disease. Differences between the groups were determined by specific statistical analyses. RESULTS: The CT genotype of DNMT3B was associated with OLP development (p = 0.012). Increased expression of DNMT3B and DNMT1 was observed in OLP compared to the control group (p = 0.014 and p = 0.001, respectively). A significant increase in DNMT3B protein levels was observed in the genotype CT in DNMT3B (C46359T) polymorphisms (p = 0.045). No DNMT3B expression differences between OLP and OIFH were observed. CONCLUSIONS: Our data show that the DNMT3B (C46359T) polymorphism is associated with OLP development. Furthermore, increased expression of the enzyme DNMT3B, an epigenetic-associated protein, is present in OLP.


Assuntos
DNA (Citosina-5-)-Metiltransferases/genética , DNA (Citosina-5-)-Metiltransferases/metabolismo , Líquen Plano Bucal/genética , Polimorfismo de Nucleotídeo Único , Proteínas Repressoras/metabolismo , Adolescente , Adulto , Idoso , DNA (Citosina-5-)-Metiltransferases/imunologia , DNA Metiltransferase 3A , Feminino , Frequência do Gene/genética , Humanos , Imuno-Histoquímica , Líquen Plano Bucal/metabolismo , Masculino , Pessoa de Meia-Idade , Mucosa Bucal/metabolismo , Proteínas Repressoras/imunologia , Adulto Jovem
6.
Rev. cuba. estomatol ; 47(3): 347-354, jul.-sep. 2010.
Artigo em Espanhol | LILACS, CUMED | ID: lil-584512

RESUMO

El carcinoma escamocelular es la neoplasia maligna más común en la cavidad bucal. Los sitios anatómicos más frecuentemente afectados son el labio inferior, los bordes laterales de lengua y el suelo de la boca. Su etiología es multifactorial, aunque está íntimamente relacionada con factores ambientales como el tabaquismo y el alcoholismo. El cuadro clínico se caracteriza generalmente por la presencia de placas blancas, placas eritematosas, placas entre eritematosas y blancas, úlceras de bordes levantados y masas exofíticas. El tratamiento consiste en la extirpación quirúrgica, la radioterapia, quimioterapia o ambos tratamientos. Este artículo presenta un caso de carcinoma escamocelular bucal en un paciente del sexo masculino, de 70 años de edad. En el mismo se describen los hallazgos clínicos, histopatológicos y el tratamiento correspondiente del caso. El diagnóstico precoz y correcto posibilitó la cura en este caso(AU)


The squamocellular carcinoma is a malignant neoplasm commonest in the buccal cavity. The more frequently involved anatomical sites are the lower lip, the tongue's lateral edges and the mouth floor. Its etiology is multifactor although it is closely related to smoking and alcoholism. Clinical picture is generally characterized by the presence of different types of white, erythematous, between erythematous and white plaques, ulcers with raised edges and exophytic masses. Treatment includes surgical removal, radiotherapy, chemotherapy or both. In present paper the case of a man aged 70 presenting with buccal squamous carcinoma describing the clinical, and the histopathologic findings and its corresponding treatment. The early and appropriate diagnosis allowed the cure of this case(AU)


Assuntos
Humanos , Masculino , Idoso , Carcinoma de Células Escamosas/etiologia , Boca/lesões , Carcinoma de Células Escamosas/tratamento farmacológico , Diagnóstico Precoce
7.
Pathobiology ; 76(3): 136-40, 2009 May.
Artigo em Inglês | MEDLINE | ID: mdl-19468253

RESUMO

OBJECTIVE: Salivary gland neoplasms pathogenesis has not been well established. DNA methylation occurs when methyl groups are added to cytosine nucleotides in specific areas of the gene by the enzyme DNA methyltransferase (DNMT). This chemical modification can alter gene expression without altering DNA sequence. While DNMT3a is mostly involved in de novo methylation, DNMT1 acts as a maintenance methyltransferase. We aimed to investigate the immunoexpression of DNMT3a and DNMT1 in minor salivary gland neoplasms, comparing it with normal tissue. MATERIAL: Forty-four formalin-fixed and paraffin-embedded samples of pleomorphic adenoma, adenoid cystic carcinoma, mucoepidermoid carcinoma and polymorphous low-grade adenocarcinoma were included in the study. The DNMT1 and DNMT3a proteins were identified by using a highly sensitive polymer-based system. RESULTS: Positive nuclear and cytoplasmic labeling for DNMT1 was observed in all samples, including the controls. Positive nuclear labeling for DNMT3a was found only in few neoplasms: 1 pleomorphic adenoma (9.0%), 2 adenoid cystic carcinoma (16.6%) and 1 mucoepidermoid (9.0%) cases. CONCLUSION: Our results were not able to demonstrate a clear correlation between DNMT1 and DNMT3a immunoexpression and salivary gland neoplasms development.


Assuntos
DNA (Citosina-5-)-Metiltransferases/biossíntese , Neoplasias das Glândulas Salivares/metabolismo , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Biomarcadores Tumorais/metabolismo , DNA (Citosina-5-)-Metiltransferase 1 , Metilação de DNA , DNA Metiltransferase 3A , Feminino , Humanos , Imuno-Histoquímica , Masculino , Pessoa de Meia-Idade , Glândulas Salivares Menores/metabolismo , Glândulas Salivares Menores/patologia , Adulto Jovem
8.
Med. oral patol. oral cir. bucal (Internet) ; 14(2): 62-68, feb. 2009. graf, tab
Artigo em Inglês | IBECS | ID: ibc-61616

RESUMO

Introduction: This study was designed to investigate the effect of oral HSV-1 shedding on the survival of allogeneichematopoietic stem cell transplanted (allo-HSCT) patients.Methods: One hundred nineteen allo-HSCT patients were included in the study and divided in three groups: beforetransplant, 100 days after transplant and 1 year of allo-HSCT. Healthy volunteers matched by age and genderwere also selected. Oral swabs were performed and the nested PCR was used to detect HSV-1 presence in the oralmucosa. In statistical analysis, chi-square test was used to test the distribution of HSV1 shedding among the threegroups. Time to death after allo-HSCT was displayed by means of the Kaplan-Meier method and the results werecompared by the log-rank test. Cox proportional hazards multivariate model was used to evaluate the survival.Results: We observed that HSV-1 shedding was similar at different points after allo-HSCT. However, HSV-1 sheddingbefore allo-HSCT was associated with worst survival rates after allo-HSCT in multivariate analysis.Conclusion: Our data demonstrates that HSV-1 shedding in oral mucosa before transplant is associated with worstsurvival rate of allo-HSCT patients (AU)


Assuntos
Humanos , Masculino , Feminino , Lactente , Pré-Escolar , Criança , Adolescente , Adulto , Pessoa de Meia-Idade , Transplante de Células-Tronco Hematopoéticas/mortalidade , Herpesvirus Humano 1/isolamento & purificação , Mucosa Bucal/virologia , Taxa de Sobrevida
9.
Med. oral patol. oral cir. bucal (Internet) ; 12(3): 233-234, may.2007. ilus
Artigo em En | IBECS | ID: ibc-054799

RESUMO

No disponible


Idiopathic osteosclerosis (IO) is described as a localized no expansible radiopacity with unknown etiology. The IO is generally asymptomatic and could appear as round, elliptical or irregular in shape. The internal aspect is usually uni- formly radiopaque. IO should be distinguished from condensing osteitis of dental origin, or other alveolar bone related radiopacities such as periapical cemental dysplasia. This condition may cause changes in tooth position or problems during orthodontic treatment. The purpose of the present study is to report a case of tooth resorption caused by ectopic eruption rote caused by IO. This condition represents a rare complication of IO


Assuntos
Feminino , Adulto , Humanos , Doenças Mandibulares/complicações , Osteosclerose/complicações , Reabsorção da Raiz/etiologia , Dente Pré-Molar , Doenças Mandibulares , Osteosclerose , Reabsorção da Raiz , Erupção Dentária , Dente Impactado
10.
Med. oral patol. oral cir. bucal (Internet) ; 11(1): 44-46, ene. 2006. ilus
Artigo em Es | IBECS | ID: ibc-042627

RESUMO

Describimos un caso clínico de varices en la mucosa yugal que fue tratado con escleroterapia. El agente esclerosante usado fue oleato de monoetanolamina. Después de la tercera sesión las varices desparecieron y la paciente mejoro


We reported a case of varicosities in the buccal mucosa treated with sclerotherapy. The sclerosant agent used was the monoethanolamineoleate. After three sessions the lesions disappeared and the patient is follow-up


Assuntos
Feminino , Pessoa de Meia-Idade , Humanos , Doenças da Boca/terapia , Mucosa Bucal/irrigação sanguínea , Soluções Esclerosantes/administração & dosagem , Varizes/terapia , Ácidos Oleicos/administração & dosagem , Endotélio Vascular , Injeções Intravenosas
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