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1.
Cells ; 9(6)2020 06 07.
Artículo en Inglés | MEDLINE | ID: mdl-32517366

RESUMEN

Exosomes are essential for several tumor progression-related processes, including the epithelial-mesenchymal transition (EMT). Long non-coding RNAs (lncRNAs) comprise a major group of exosomal components and regulate the neoplastic development of several cancer types; however, the progressive role of exosomal lncRNAs in bladder cancer have rarely been addressed. In this study, we identified two potential aggressiveness-promoting exosomal lncRNAs, LINC00960 and LINC02470. Exosomes derived from high-grade bladder cancer cells enhanced the viability, migration, invasion and clonogenicity of recipient low-grade bladder cancer cells and activated major EMT-upstream signaling pathways, including ß-catenin signaling, Notch signaling, and Smad2/3 signaling pathways. Nevertheless, LINC00960 and LINC02470 were expressed at significantly higher levels in T24 and J82 cells and their secreted exosomes than in TSGH-8301 cells. Moreover, exosomes derived from LINC00960 knockdown or LINC02470 knockdown T24 cells significantly attenuated the ability of exosomes to promote cell aggressiveness and activate EMT-related signaling pathways in recipient TSGH-8301 cells. Our findings indicate that exosome-derived LINC00960 and LINC02470 from high-grade bladder cancer cells promote the malignant behaviors of recipient low-grade bladder cancer cells and induce EMT by upregulating ß-catenin signaling, Notch signaling, and Smad2/3 signaling. Both lncRNAs may serve as potential liquid biomarkers for the prognostic surveillance of bladder cancer progression.


Asunto(s)
Transición Epitelial-Mesenquimal/genética , Exosomas/metabolismo , ARN Largo no Codificante/metabolismo , Neoplasias de la Vejiga Urinaria/genética , Neoplasias de la Vejiga Urinaria/patología , Comunicación Celular/efectos de los fármacos , Línea Celular Tumoral , Movimiento Celular/efectos de los fármacos , Supervivencia Celular/efectos de los fármacos , Medios de Cultivo Condicionados/farmacología , Regulación Neoplásica de la Expresión Génica , Humanos , Modelos Biológicos , Clasificación del Tumor , Invasividad Neoplásica , ARN Largo no Codificante/genética , Reproducibilidad de los Resultados , Neoplasias de la Vejiga Urinaria/ultraestructura
2.
Kaohsiung J Med Sci ; 27(8): 348-52, 2011 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-21802647

RESUMEN

Hibernoma is a rare benign tumor that arises from the vestiges of fetal brown fat. We present a case of interscapular hibernoma. Computed tomography scan showed a well-circumscribed, hypodense mass with peripheral enhancement, and magnetic resonance imaging revealed intermediate high T1 and T2 signal intensities with incomplete fat suppression. Although it is rare, hibernoma should be included in the differential diagnosis of lipomatous soft-tissue tumors. This is a benign tumor with no malignant potential. Complete excision is the treatment choice.


Asunto(s)
Tejido Adiposo Pardo/patología , Lipoma/diagnóstico , Neoplasias de los Tejidos Blandos/diagnóstico , Tejido Adiposo Pardo/diagnóstico por imagen , Adulto , Diagnóstico Diferencial , Humanos , Lipoma/diagnóstico por imagen , Lipoma/patología , Imagen por Resonancia Magnética , Masculino , Neoplasias de los Tejidos Blandos/diagnóstico por imagen , Neoplasias de los Tejidos Blandos/patología , Tomografía Computarizada por Rayos X
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