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1.
Clinics (Sao Paulo) ; 66(6): 965-72, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21808860

RESUMO

OBJECTIVE: To analyze glucose transporter 1 expression patterns in malignant tumors of various cell types and evaluate their diagnostic value by immunohistochemistry. INTRODUCTION: Glucose is the major source of energy for cells, and glucose transporter 1 is the most common glucose transporter in humans. Glucose transporter 1 is aberrantly expressed in several tumor types. Studies have implicated glucose transporter 1 expression as a prognostic and diagnostic marker in tumors, primarily in conjunction with positron emission tomography scan data. METHODS: Immunohistochemistry for glucose transporter 1 was performed in tissue microarray slides, comprising 1955 samples of malignant neoplasm from different cell types. RESULTS: Sarcomas, lymphomas, melanomas and hepatoblastomas did not express glucose transporter 1. Forty-seven per cent of prostate adenocarcinomas were positive, as were 29% of thyroid, 10% of gastric and 5% of breast adenocarcinomas. Thirty-six per cent of squamous cell carcinomas of the head and neck were positive, as were 42% of uterine cervix squamous cell carcinomas. Glioblastomas and retinoblastomas showed membranous glucose transporter 1 staining in 18.6% and 9.4% of all cases, respectively. Squamous cell carcinomas displayed membranous expression, whereas adenocarcinomas showed cytoplasmic glucose transporter 1 expression. CONCLUSION: Glucose transporter 1 showed variable expression in various tumor types. Its absence in sarcomas, melanomas, hepatoblastomas and lymphomas suggests that other glucose transporters mediate the glycolytic pathway in these tumors. The data suggest that glucose transporter 1 is a valuable immunohistochemical marker that can be used to identify patients for evaluation by positron emission tomography scan. The function of cytoplasmic glucose transporter 1 in adenocarcinomas must be further examined.


Assuntos
Biomarcadores Tumorais/metabolismo , Carcinoma/metabolismo , Transportador de Glucose Tipo 1/metabolismo , Neoplasias Neuroepiteliomatosas/metabolismo , Carcinoma/diagnóstico , Humanos , Imuno-Histoquímica , Neoplasias Neuroepiteliomatosas/diagnóstico , Valor Preditivo dos Testes , Prognóstico , Análise Serial de Tecidos
2.
Clinics ; Clinics;66(6): 965-972, 2011. ilus, graf, tab
Artigo em Inglês | LILACS | ID: lil-594363

RESUMO

OBJECTIVE: To analyze glucose transporter 1 expression patterns in malignant tumors of various cell types and evaluate their diagnostic value by immunohistochemistry. INTRODUCTION: Glucose is the major source of energy for cells, and glucose transporter 1 is the most common glucose transporter in humans. Glucose transporter 1 is aberrantly expressed in several tumor types. Studies have implicated glucose transporter 1 expression as a prognostic and diagnostic marker in tumors, primarily in conjunction with positron emission tomography scan data. METHODS: Immunohistochemistry for glucose transporter 1 was performed in tissue microarray slides, comprising 1955 samples of malignant neoplasm from different cell types. RESULTS: Sarcomas, lymphomas, melanomas and hepatoblastomas did not express glucose transporter 1. Fortyseven per cent of prostate adenocarcinomas were positive, as were 29 percent of thyroid, 10 percent of gastric and 5 percent of breast adenocarcinomas. Thirty-six per cent of squamous cell carcinomas of the head and neck were positive, as were 42 percent of uterine cervix squamous cell carcinomas. Glioblastomas and retinoblastomas showed membranous glucose transporter 1 staining in 18.6 percent and 9.4 percent of all cases, respectively. Squamous cell carcinomas displayed membranous expression, whereas adenocarcinomas showed cytoplasmic glucose transporter 1 expression. CONCLUSION: Glucose transporter 1 showed variable expression in various tumor types. Its absence in sarcomas, melanomas, hepatoblastomas and lymphomas suggests that other glucose transporters mediate the glycolytic pathway in these tumors. The data suggest that glucose transporter 1 is a valuable immunohistochemical marker that can be used to identify patients for evaluation by positron emission tomography scan. The function of cytoplasmic glucose transporter 1 in adenocarcinomas must be further examined.


Assuntos
Humanos , Carcinoma/metabolismo , Transportador de Glucose Tipo 1/metabolismo , Neoplasias Neuroepiteliomatosas/metabolismo , Biomarcadores Tumorais/metabolismo , Carcinoma/diagnóstico , Imuno-Histoquímica , Neoplasias Neuroepiteliomatosas/diagnóstico , Valor Preditivo dos Testes , Prognóstico , Análise Serial de Tecidos
3.
Pediatr Dev Pathol ; 11(6): 479-81, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-17990912

RESUMO

Primary uveal-tract neoplasms are extremely rare in childhood; the most common lesions found are melanocytic. We report here the case of a 7-year-old girl who underwent enucleation of the right eye with clinical suspicion of choroid melanoma as a result of a ciliary body mass that extended to the posterior chamber. Histologically, the neoplasm featured spindle cell morphology, atypia, and mitoses. The tumor expressed smooth muscle alpha actin, pan-actin HHF-35, and desmin, whereas immunohistochemistry for melanocytic markers, such as S-100, Melan-A, and HMB-45, was negative. Based on these features, the diagnosis of leiomyosarcoma of the ciliary body was firmly established. Although several leiomyomas have been reported in the literature, there are only 2 previously reported cases of primary leiomyosarcoma of the uveal tract. Immunohistochemical expression of muscle proteins allowed distinction from the most common melanocytic tumors arising in this location.


Assuntos
Corpo Ciliar/patologia , Leiomiossarcoma/patologia , Neoplasias Uveais/patologia , Biomarcadores Tumorais/análise , Proliferação de Células , Criança , Corioide/patologia , Corpo Ciliar/química , Corpo Ciliar/cirurgia , Diagnóstico Diferencial , Enucleação Ocular , Feminino , Humanos , Imuno-Histoquímica , Leiomiossarcoma/química , Leiomiossarcoma/cirurgia , Melanoma/diagnóstico , Neoplasias Uveais/química , Neoplasias Uveais/cirurgia
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