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1.
Biotechnol Bioeng ; 114(12): 2868-2882, 2017 12.
Artículo en Inglés | MEDLINE | ID: mdl-28755500

RESUMEN

Constitutive activation of Wnt signaling plays an important role in colorectal and liver tumorigenesis. Cell-based assays using synthetic TCF/LEF (T-cell factor/lymphoid enhancer factor) reporters, as readouts of ß-catenin/TCF-dependent transcriptional activity, have contributed greatly to the discovery of small molecules that modulate Wnt signaling. In the present study, we report a novel screening method, called a bidirectional dual reporter assay. Integrated transcriptome analysis identified a histidine ammonia-lyase gene (HAL) that was negatively regulated by ß-catenin/TCF-dependent transcriptional activity. We leveraged a promoter region of the HAL gene as another transcriptional readout of Wnt signaling. Cells stably expressing both an optimized HAL reporter and the TCF/LEF reporter enabled bidirectional reporter activities in response to Wnt signaling. Increased HAL reporter activity and decreased TCF/LEF reporter activity were observed simultaneously in the cells when ß-catenin/TCF7L2 was inhibited. Notably, this method could decrease the number of false positives observed when screening an inhibitor library compared with the conventional TCF/LEF assay. We found that Brefeldin A, a disruptor of the Golgi apparatus, inhibited the Wnt/ß-catenin signaling pathway. The utility of our system could be expanded to examine other disease-associated pathways beyond the Wnt/ß-catenin signaling pathway.


Asunto(s)
Brefeldino A/administración & dosificación , Genes Reporteros/genética , Ensayos Analíticos de Alto Rendimiento/métodos , Histidina Amoníaco-Liasa/genética , Regiones Promotoras Genéticas/genética , Proteínas Wnt/antagonistas & inhibidores , Vía de Señalización Wnt/efectos de los fármacos , Bioensayo , Diseño de Fármacos , Evaluación Preclínica de Medicamentos/métodos , Proteínas Wnt/genética , Vía de Señalización Wnt/genética
2.
Eur J Gastroenterol Hepatol ; 22(2): 228-33, 2010 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-19923997

RESUMEN

We report a male patient with double advanced tumors in the jejunum and descending colon and multiple lung tumors. The intestinal cancers were surgically resected. Immunoprofiling of the specimens revealed a rare phenotype: the jejunal cancer was positive for cytokeratin (CK) 7, partially positive for CK20, and Cdx-2-negative, whereas the colon cancer was CK7(+), CK20(-), and Cdx-2(-). Biopsied lung tumor was diagnosed as tubular adenocarcinoma, and CK7(+)/CK20(+)/Cdx-2(-). Together with clinical information, we deduced that the jejunal adenocarcinoma had presumably metastasized to the lung. Moreover, postoperative oxaliplatin, including chemotherapy, significantly reduced the lung metastases, suggesting that this regimen is a promising treatment option for advanced small bowel adenocarcinoma.


Asunto(s)
Adenocarcinoma/secundario , Biomarcadores de Tumor/análisis , Neoplasias del Colon/patología , Inmunohistoquímica , Neoplasias del Yeyuno/patología , Neoplasias Pulmonares/secundario , Neoplasias Primarias Múltiples , Adenocarcinoma/química , Adenocarcinoma/genética , Adenocarcinoma/terapia , Antineoplásicos/administración & dosificación , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapéutico , Biopsia , Factor de Transcripción CDX2 , Quimioterapia Adyuvante , Colectomía , Neoplasias del Colon/química , Neoplasias del Colon/genética , Neoplasias del Colon/terapia , Resultado Fatal , Fluorouracilo/uso terapéutico , Proteínas de Homeodominio/análisis , Humanos , Neoplasias del Yeyuno/química , Neoplasias del Yeyuno/genética , Neoplasias del Yeyuno/terapia , Queratina-20/análisis , Queratina-7/análisis , Leucovorina/uso terapéutico , Neoplasias Pulmonares/química , Neoplasias Pulmonares/genética , Neoplasias Pulmonares/terapia , Escisión del Ganglio Linfático , Masculino , Persona de Mediana Edad , Compuestos Organoplatinos/administración & dosificación , Compuestos Organoplatinos/uso terapéutico , Oxaliplatino , Fenotipo , Tomografía Computarizada por Rayos X , Resultado del Tratamiento
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