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1.
Pediatr Emerg Care ; 36(11): e659-e664, 2020 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-31688704

RESUMO

The Pediatric Emergency Care Applied Research Network rule helps emergency physicians identify very low-risk children with minor head injury who can forgo head computed tomography. This rule contributes to reduction in lifetime risk of radiation-induced cancers while minimizing missing clinically important traumatic brain injury. However, in intermediate-risk children, decisions on whether to perform computed tomography remain at the emergency physicians' discretion. To reduce this gray zone, this review summarizes evidence for risk stratification of intermediate-risk children with minor head injury.


Assuntos
Traumatismos Craniocerebrais/diagnóstico por imagem , Tomada de Decisões , Serviço Hospitalar de Emergência , Medição de Risco , Tomografia Computadorizada por Raios X , Criança , Humanos , Doses de Radiação
2.
Oncogene ; 37(32): 4443-4454, 2018 08.
Artigo em Inglês | MEDLINE | ID: mdl-29720727

RESUMO

Gene mutations play critical roles during cancer development and progression, and therefore represent targets for precision medicine. Here we recapitulated the pharmacogenomic data to delineate novel candidates for actionable mutations and therapeutic target drugs. As a proof-of-concept, we demonstrated that the loss-of-function of SULF2 by mutation (N491K) or inhibition enhanced sorafenib sensitivity in liver cancer cells and in vivo mouse models. This effect was mediated by deregulation of EGFR signaling and downstream expression of LCN2. We also report that the liver cancer patients non-responding to sorafenib treatment exhibit higher expression of SULF2 and LCN2. In conclusion, we suggest that SULF2 plays a key role in sorafenib susceptibility and resistance in liver cancer via deregulation of LCN2. Diagnostic or therapeutic targeting of SULF2 (e.g., OKN-007) and/or LCN2 can be a novel precision strategy for sorafenib treatment in cancer patients.


Assuntos
Neoplasias Hepáticas/tratamento farmacológico , Neoplasias Hepáticas/genética , Sorafenibe/farmacologia , Sulfotransferases/genética , Animais , Linhagem Celular Tumoral , Receptores ErbB/genética , Humanos , Lipocalina-2/genética , Camundongos , Mutação/genética , Farmacogenética/métodos , Transdução de Sinais/genética , Sulfatases
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