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1.
Eur Surg Res ; 48(3): 121-30, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22538557

RESUMO

Cancer is rapidly becoming the worldwide leading cause of premature death. Iconographic techniques have traditionally provided information on tumor anatomy. The recent introduction of functional and molecular imaging techniques allows probing tumor physiology and biology in addition to mere anatomical description. In addition to the research implications, these novel imaging techniques offer early response assessment and target visualization which, in the era of personalized medicine, may offer significant advances in cancer therapy. Here, we provide an overview of the most important developments in cancer imaging, with a focus on the clinical applications.


Assuntos
Neoplasias/diagnóstico , Proliferação de Células , Imagem de Difusão por Ressonância Magnética , Fluordesoxiglucose F18 , Humanos , Aumento da Imagem , Linfonodos/patologia , Imagem Multimodal , Tomografia por Emissão de Pósitrons , Tomografia Computadorizada por Raios X
2.
Br J Cancer ; 102(5): 837-43, 2010 Mar 02.
Artigo em Inglês | MEDLINE | ID: mdl-20125158

RESUMO

BACKGROUND: Recently, low-molecular-weight heparins (LMWHs) were found to confer a survival advantage in cancer patients. The mechanism underlying this observation is unclear, but may involve inhibition of tumour angiogenesis. We aimed to examine the effects of nadroparin on tumour angiogenesis using a dorsal skinfold window chamber model in the Syrian hamster. METHODS: AMel-3 and HAP-T1 tumours were grown in donor animals and fragments implanted in the window chambers. Animals (N=46) were treated with 200 IU of nadroparin or saline for 10 days. Repeated intravital fluorescence microscopy was performed to calculate functional microcirculatory parameters: number (N) and length (L) of microvessels, vascular area fraction (AF), and red blood cell velocity (V). Microvessel density (MVD), fractal dimension, and pericyte coverage were assessed histologically. RESULTS: Active angiogenesis was observed in control animals, resulting in a significant increase in N, L, and AF. In nadroparin-treated animals, however, N and L did not increase whereas AF decreased significantly. Both groups showed an initial increase in V, but nadroparin treatment resulted in an earlier decrease in red blood cell velocity over time. Compared with control animals, nadroparin-treated animals showed a significantly lower MVD and fractal dimension but significantly higher pericyte coverage index (PCI). CONCLUSIONS: Taken together, these results suggest that the LMWH nadroparin inhibits tumour angiogenesis and results in microvessel normalisation.


Assuntos
Anticoagulantes/farmacologia , Melanoma Experimental/irrigação sanguínea , Nadroparina/farmacologia , Neovascularização Patológica/prevenção & controle , Neoplasias Pancreáticas/irrigação sanguínea , Neoplasias Cutâneas/prevenção & controle , Animais , Velocidade do Fluxo Sanguíneo/efeitos dos fármacos , Cricetinae , Eritrócitos/efeitos dos fármacos , Técnicas Imunoenzimáticas , Mesocricetus , Microcirculação/efeitos dos fármacos
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