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1.
Histopathology ; 79(2): 252-259, 2021 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-33657658

RESUMO

AIMS: Because serous cystadenoma (SCA) does not usually require excision, it is critical to distinguish it from differential diagnoses which do, especially neuroendocrine tumour (NET). The gold standard for diagnosing SCA is assessment of endoscopic ultrasound-guided fine needle aspiration/biopsy (EUS-FNAB) material. Inhibin immunohistochemistry aids this assessment, but such positivity is not absolutely sensitive or specific to SCA. The following is the largest known study of SCA EUS-FNAB specimens and the first to compare four potential SCA immunomarkers between themselves and inhibin, compared against NET. METHODS AND RESULTS: Immunohistochemistry for calponin, mucin 6 (MUC6), glucose transporter 1 (GLUT1) and vascular endothelial growth factor A (VEGFA) was performed on 30 EUS-FNAB and three resection specimens of SCA and 32 EUS-FNAB specimens of NET. GLUT1 and VEGFA were suboptimal as diagnostic immunomarkers of SCA, being expressed by 10 and 44% of NETs, respectively. Further, their expression by cellular constituents of blood which often contaminate EUS-FNAB specimens hampered identification of neoplastic cells, especially in hypocellular samples. While 19% of NETs showed nuclear MUC6 positivity, cytoplasmic expression of the protein showed 100% specificity and sensitivity as an SCA marker. However, assessing MUC6 in EUS-FNAB specimens must also consider the protein's focal expression in physiological pancreatic, gastric or duodenal tissues, which can contaminate these specimens. Calponin was less sensitive (71% versus 100%) but more specific (100% versus 91%) than inhibin, although easier to assess in EUS-FNAB specimens than MUC6. CONCLUSIONS: Of the four potential immunomarkers of SCA suggested by the existing literature, calponin and MUC6 are useful complementary studies to inhibin for application to EUS-FNAB specimens.


Assuntos
Proteínas de Ligação ao Cálcio/metabolismo , Cistadenoma Seroso/diagnóstico , Cistadenoma Seroso/imunologia , Aspiração por Agulha Fina Guiada por Ultrassom Endoscópico , Inibinas/metabolismo , Proteínas dos Microfilamentos/metabolismo , Mucina-6/metabolismo , Adolescente , Adulto , Idoso , Biomarcadores Tumorais , Proteínas de Ligação ao Cálcio/imunologia , Estudos de Coortes , Cistadenoma Seroso/patologia , Duodeno/patologia , Aspiração por Agulha Fina Guiada por Ultrassom Endoscópico/instrumentação , Feminino , Transportador de Glucose Tipo 1/metabolismo , Humanos , Imuno-Histoquímica , Inibinas/imunologia , Masculino , Proteínas dos Microfilamentos/imunologia , Pessoa de Meia-Idade , Tumores Neuroendócrinos/patologia , Pâncreas/patologia , Estômago/patologia , Sinaptofisina/metabolismo , Fator A de Crescimento do Endotélio Vascular/metabolismo , Calponinas
2.
Dig Dis Sci ; 54(12): 2549-60, 2009 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-19130224

RESUMO

Cochinchina momordica seed extract (SKMS10), which is composed of the major compounds momordica saponins, has been evaluated for its gastroprotective effects in rat models of acute gastric mucosal damage. Ethanol and water immersion restraint stress (WRS) induced gastric damage, including hemorrhages and edema, was significantly attenuated by pretreatment with SK-MS10. In addition, SK-MS10 reduced increases of mucosal myeloperoxidase (MPO), IL-1ß, and TNFα levels and the expression of cPLA(2), and 5-LOX induced by ethanol or WRS. SK-MS10 also increased hexosamine, adherent mucus, and the expression of MUC5AC. Furthermore, SK-MS10 enhanced the mucosal expression of the CGRP gene and its serum levels.N(G)-methyl L-arginine (L-NMMA) or capsaicin desensitization reversed the SK-MS10-induced gastroprotection effect. These results suggest that SK-MS10 is a gastroprotective agent against acute gastric mucosal damage by suppressing proinflammatory cytokines, downregulating cPLA(2), 5-LOX, and increasing the synthesis of mucus. Furthermore, CGRP-NO pathway was found to play an important role in these gastroprotective effects of SK-MS10.


Assuntos
Araquidonato 5-Lipoxigenase/metabolismo , Peptídeo Relacionado com Gene de Calcitonina/metabolismo , Mucosa Gástrica/efeitos dos fármacos , Fármacos Gastrointestinais/farmacologia , Fosfolipases A2 do Grupo IV/metabolismo , Momordica , Extratos Vegetais/farmacologia , Transdução de Sinais/efeitos dos fármacos , Úlcera Gástrica/prevenção & controle , Animais , Peptídeo Relacionado com Gene de Calcitonina/sangue , Peptídeo Relacionado com Gene de Calcitonina/genética , Ciclo-Oxigenase 2/metabolismo , Citoproteção , Dinoprostona/metabolismo , Modelos Animais de Doenças , Regulação para Baixo , Etanol , Mucosa Gástrica/enzimologia , Mucosa Gástrica/patologia , Hexosaminas/metabolismo , Mediadores da Inflamação/metabolismo , Interleucina-1beta/metabolismo , Leucotrieno B4/metabolismo , Masculino , Mucina-5AC/metabolismo , Mucina-6/metabolismo , Óxido Nítrico/metabolismo , Óxido Nítrico Sintase/antagonistas & inibidores , Óxido Nítrico Sintase/metabolismo , Óxido Nítrico Sintase Tipo I , Peroxidase/metabolismo , RNA Mensageiro/metabolismo , Ratos , Ratos Sprague-Dawley , Restrição Física , Sementes , Células Receptoras Sensoriais/efeitos dos fármacos , Células Receptoras Sensoriais/metabolismo , Úlcera Gástrica/enzimologia , Úlcera Gástrica/etiologia , Úlcera Gástrica/patologia , Fatores de Tempo , Fator de Necrose Tumoral alfa/metabolismo
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