Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Más filtros











Intervalo de año de publicación
1.
Biol Res ; 51(1): 19, 2018 06 22.
Artículo en Inglés | MEDLINE | ID: mdl-29933754

RESUMEN

Concerns have been raised about this article [1] relating to the appropriateness of the use of the shRNA (5'-GCGGAGGGTTTGAAAGAATATCTCGAGATATTCTTTCAAACCCTCCGCTTTTTT-3') as a non-targeting control and similarities in text and formatting with other published articles. This is currently under investigation and appropriate editorial action will be taken once the investigation is concluded. The authors agree.

2.
Biol Res ; 48: 18, 2015 03 19.
Artículo en Inglés | MEDLINE | ID: mdl-25889525

RESUMEN

BACKGROUND: Ubiquitin Specific Peptidase 39 (USP39) is a 65 kDa SR-related protein involved in RNA splicing. Previous studies showed that USP39 is related with tumorigenesis of human breast cancer cells. RESULTS: In the present study, we investigated the functions of USP39 in human hepatocellular carcinoma (HCC) cell line SMMC-7721. We knocked down the expression of USP39 through lentivirus mediated RNA interference. The results of qRT-PCR and western blotting assay showed that both the mRNA and protein levels were suppressed efficiently after USP39 specific shRNA was delivered into SMMC-7721 cells. Cell growth was significantly inhibited as determined by MTT assay. Crystal violet staining indicated that colony numbers and sizes were both reduced after knock-down of USP39. Furthermore, suppression of USP39 arrested cell cycle progression at G2/M phase in SMMC-7721cells. In addition, Annexin V showed that downregulation of USP39 significantly increased the population of apoptotic cells. CONCLUSIONS: All our results suggest that USP39 is important for HCC cell proliferation and is a potential target for molecular therapy of HCC.


Asunto(s)
Carcinoma Hepatocelular/patología , Ciclo Celular , Proliferación Celular , Lentivirus/genética , Neoplasias Hepáticas/patología , Proteínas de Neoplasias/metabolismo , Interferencia de ARN/fisiología , Proteasas Ubiquitina-Específicas/metabolismo , Apoptosis , Western Blotting , Carcinoma Hepatocelular/enzimología , Ciclo Celular/genética , Línea Celular Tumoral , Proliferación Celular/genética , Regulación Neoplásica de la Expresión Génica/genética , Técnicas de Silenciamiento del Gen , Silenciador del Gen , Técnicas de Transferencia de Gen , Humanos , Técnicas In Vitro , Neoplasias Hepáticas/enzimología , Proteínas de Neoplasias/genética , Reacción en Cadena en Tiempo Real de la Polimerasa , Proteasas Ubiquitina-Específicas/genética
3.
Biol. Res ; 48: 1-7, 2015. ilus, graf
Artículo en Inglés | LILACS | ID: biblio-950782

RESUMEN

BACKGROUND: Ubiquitin Specific Peptidase 39 (USP39) is a 65 kDa SR-related protein involved in RNA splicing. Previous studies showed that USP39 is related with tumorigenesis of human breast cancer cells. RESULTS: In the present study, we investigated the functions of USP39 in human hepatocellular carcinoma (HCC) cell line SMMC-7721. We knocked down the expression of USP39 through lentivirus mediated RNA interference. The results of qRT-PCR and western blotting assay showed that both the mRNA and protein levels were suppressed efficiently after USP39 specific shRNA was delivered into SMMC-7721 cells. Cell growth was significantly inhibited as determined by MTT assay. Crystal violet staining indicated that colony numbers and sizes were both reduced after knock-down of USP39. Furthermore, suppression of USP39 arrested cell cycle progression at G2/M phase in SMMC-7721cells. In addition, Annexin V showed that downregulation of USP39 significantly increased the population of apoptotic cells. CONCLUSIONS: All our results suggest that USP39 is important for HCC cell proliferation and is a potential target for molecular therapy of HCC.


Asunto(s)
Humanos , Ciclo Celular , Carcinoma Hepatocelular/patología , Lentivirus/genética , Interferencia de ARN/fisiología , Proliferación Celular , Proteasas Ubiquitina-Específicas/metabolismo , Neoplasias Hepáticas/patología , Proteínas de Neoplasias/metabolismo , Técnicas In Vitro , Regulación Neoplásica de la Expresión Génica/genética , Ciclo Celular/genética , Western Blotting , Apoptosis , Técnicas de Transferencia de Gen , Carcinoma Hepatocelular/enzimología , Silenciador del Gen , Línea Celular Tumoral , Proliferación Celular/genética , Técnicas de Silenciamiento del Gen , Reacción en Cadena en Tiempo Real de la Polimerasa , Proteasas Ubiquitina-Específicas/genética , Neoplasias Hepáticas/enzimología , Proteínas de Neoplasias/genética
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA