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1.
Endocr Relat Cancer ; 14(2): 463-71, 2007 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-17639059

RESUMO

Pheochromocytomas are catecholamine-producing tumors that can occur in the context of von Hippel-Lindau syndrome (VHL) and multiple endocrine neoplasia type 2 (MEN2). Pheochromocytomas in these two syndromes differ in histopathological features, catecholamine metabolism, and clinical phenotype. To further investigate the nature of these differences, we compared the global protein expressions of 8 MEN2A-associated pheochromocytomas with 11 VHL-associated pheochromocytomas by two-dimensional gel electrophoresis proteomic profiling followed by sequencing and identification of differentially expressed proteins. Although both types of pheochromocytoma shared similarities in their protein expression patterns, the expression of several proteins was distinctly different between VHL- and MEN2A-associated pheochromocytomas. We identified several of these differentially expressed proteins. One of the proteins with higher expression in MEN2-associated tumors was chromogranin B, of which the differential expression was confirmed by western blot analysis. Our results expand the evidence for proteomic differences between these two tumor entities, and suggest that VHL-associated pheochromocytomas may be deficient in fundamental machinery for catecholamine storage. In light of these new findings, as well as existing evidence for differences between both types of pheochromocytomas, we propose that these tumors may have different developmental origins.


Assuntos
Neoplasias das Glândulas Suprarrenais/metabolismo , Cromogranina B/metabolismo , Neoplasia Endócrina Múltipla Tipo 2a/metabolismo , Feocromocitoma/metabolismo , Doença de von Hippel-Lindau/metabolismo , Adolescente , Neoplasias das Glândulas Suprarrenais/patologia , Adulto , Catecolaminas/metabolismo , Criança , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Neoplasia Endócrina Múltipla Tipo 2a/patologia , Feocromocitoma/patologia , Análise Serial de Proteínas , Proteômica , Doença de von Hippel-Lindau/patologia
2.
J Child Neurol ; 17(5): 341-6, 2002 May.
Artigo em Inglês | MEDLINE | ID: mdl-12150580

RESUMO

Neural tube defects are common birth defects, the frequency of which appears to be reduced by maternal supplementation and/or fortification of folic acid. Latin Americans have a high incidence of neural tube defects. We surveyed the dietary intake of Honduran women of childbearing age using a 24-hour dietary recall questionnaire in inner-city, town, and country areas. We randomly checked blood folate in the surveyed population to compare to the normal range for the US population. Normal US recommended dietary allowance intake of folate was documented in association with a low intake of many other essential nutrients. There also were significant differences for nutrient intakes in city, town, and country areas. Blood folate levels in all locations were in the low normal range when compared to the presupplementation/prefortification US population. Our data support using an established folic acid fortification public health initiative to decrease the prevalence of neural tube defects in Honduras.


Assuntos
Ingestão de Energia , Deficiência de Ácido Fólico/sangue , Deficiência de Ácido Fólico/epidemiologia , Adolescente , Adulto , Feminino , Honduras/epidemiologia , Humanos , Recém-Nascido , Pessoa de Meia-Idade , Gravidez
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