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1.
Gut Liver ; 16(6): 942-951, 2022 11 15.
Artículo en Inglés | MEDLINE | ID: mdl-35611666

RESUMEN

Background/Aims: Chronic enteropathy associated with SLCO2A1 gene (CEAS), an inherited disease characterized by nonspecific intestinal ulcers, has emerged in the Japanese population via loss-of-function mutations in the SLCO2A1 gene. We aimed to investigate the clinical and genetic characteristics of Korean patients diagnosed with CEAS. Methods: From July 2018 to July 2021, we performed Sanger sequencing of the SLCO2A1 gene in 46 patients with chronic intestinal ulcers. CEAS was confirmed based on known SLCO2A1 mutations. We summarized the clinical characteristics of patients with confirmed CEAS. Results: Fourteen out of 46 patients (30.4%) had genetically confirmed CEAS, and two SLCO2A1 variants were detected (splicing site variant c.940+1G>A and nonsense mutation [p.R603X] in SLCO2A1). Twelve patients (85.7%) were females and the median age at diagnosis of CEAS was 44.5 years. All patients presented with abdominal pain, and 13 patients (92.9%) presented with anemia (median hemoglobin, 9.6 g/dL). Ten patients (71.4%) had hypoalbuminemia (median, 2.7 g/dL). The most commonly involved site was the ileum (13/14, 92.9%). Manifestations of primary hypertrophic osteoarthropathy (PHO), such as digital clubbing, pachydermia, and periostosis were observed in five patients (28.6%) and two male patients and one female patient satisfied all major PHO diagnostic criteria. Conclusions: The clinical and genetic characteristics of Korean patients with confirmed CEAS were similar to those reported in the literature. CEAS should be considered in the differential diagnosis for patients with unexplained chronic nonspecific ulcers of the small intestine.


Asunto(s)
Enfermedades Inflamatorias del Intestino , Transportadores de Anión Orgánico , Humanos , Masculino , Femenino , Adulto , Úlcera , Transportadores de Anión Orgánico/genética , Intestino Delgado , Mutación , República de Corea
2.
J Gen Virol ; 94(Pt 3): 497-506, 2013 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-23175241

RESUMEN

Epstein-Barr virus (EBV) is a herpesvirus associated with lymphomas and carcinomas. While EBV-associated epithelial cell lines are good model systems to investigate the role of EBV in carcinoma, only a few cell lines are available as they are hard to acquire. A greater variety of naturally EBV-infected cell lines which are derived from tumour patients are needed to represent various features of EBVaGC. We characterized cell line YCCEL1, established from a Korean EBVaGC patient, to ascertain whether it can be used to study the roles of EBV in EBVaGC. The expression of EBV genes and cell surface markers was examined by in situ hybridization, RT-PCR, Western blot analysis, immunofluorescence assay and Northern blot analysis. EBV episomal status was analysed by Southern blotting and real-time PCR. This cell line expressed EBV nuclear antigen 1 (EBNA1) and latent membrane protein 2A (LMP2A), but not EBNA2, LMP2B nor LMP1. The majority of the lytic proteins were not detected in YCCEL1 cells either before or after treatment with 12-O-tetradecanoylphorbol-13-acetate. YCCEL1 cells expressed BART microRNAs (miRNAs) at high level but did not express BHRF1 miRNAs. YCCEL1 cells expressed cytokeratin, but not CD21 and CD19, suggesting CD21-independent EBV infection. The latent EBV gene and EBV miRNA expression pattern of YCCEL1 cells closely resembled that of general EBVaGC cases. Our results support the value of YCCEL1 cells as a good model system to study the role of EBV in gastric carcinogenesis.


Asunto(s)
Carcinoma/virología , Herpesvirus Humano 4/fisiología , Neoplasias Gástricas/virología , Southern Blotting , Línea Celular Tumoral , Regulación de la Expresión Génica/fisiología , Genoma Viral , Humanos , MicroARNs/genética , MicroARNs/metabolismo , Reacción en Cadena en Tiempo Real de la Polimerasa , Receptores de Complemento 3d/genética , Receptores de Complemento 3d/metabolismo , Proteínas Virales/genética , Proteínas Virales/metabolismo
3.
J Clin Gastroenterol ; 46(10): e87-91, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-22810108

RESUMEN

OBJECTIVE: The risk of malignancy after transplantation is regarded to be higher than in the general population. The aim of this study was to evaluate the frequency of gastric cancer in renal transplant recipients. METHODS: A total of 820 renal transplantation recipients were invited for gastric cancer screening. Frequencies of gastric cancer in this cohort and in 10,080 asymptomatic subjects were compared. Cancer specimens were examined for Epstein-Barr virus by in situ hybridization. RESULTS: A total of 509 recipients (mean age, 48.1 ± 10.7 y; men, 56.8%) participated. Fifteen (2.9%) and 10 (0.1%) cases of adenocarcinoma were identified among recipients and controls, respectively (P<0.001; odds ratio, 30.58). Early gastric cancer was detected in 9 of the 15 recipients, and 4 of the 9 were treated by endoscopic resection. Recipient age was found to be a significant factor of gastric cancer development. In cancer tissues, Epstein-Barr virus was detected in 5 (33.3%) renal recipients and in 1 (10%) of the controls, respectively. CONCLUSIONS: The frequency of gastric cancer was found to be higher in renal recipients than in controls. Gastric cancer screening should be considered after transplantation, because it would provide cure by minimally invasive treatment.


Asunto(s)
Adenocarcinoma/epidemiología , Inmunosupresores/efectos adversos , Trasplante de Riñón/inmunología , Neoplasias Gástricas/epidemiología , Adenocarcinoma/cirugía , Adenocarcinoma/virología , Adulto , Factores de Edad , Anciano , Anciano de 80 o más Años , Intervalos de Confianza , Infecciones por Virus de Epstein-Barr/epidemiología , Femenino , Gastroscopía , Infecciones por Helicobacter/epidemiología , Helicobacter pylori , Herpesvirus Humano 4 , Humanos , Trasplante de Riñón/efectos adversos , Masculino , Persona de Mediana Edad , Oportunidad Relativa , Vigilancia de la Población , República de Corea/epidemiología , Neoplasias Gástricas/cirugía , Neoplasias Gástricas/virología , Factores de Tiempo , Adulto Joven
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