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1.
Eur Surg Res ; 48(3): 121-30, 2012.
Article in English | MEDLINE | ID: mdl-22538557

ABSTRACT

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.


Subject(s)
Neoplasms/diagnosis , Cell Proliferation , Diffusion Magnetic Resonance Imaging , Fluorodeoxyglucose F18 , Humans , Image Enhancement , Lymph Nodes/pathology , Multimodal Imaging , Positron-Emission Tomography , Tomography, X-Ray Computed
2.
Br J Cancer ; 102(5): 837-43, 2010 Mar 02.
Article in English | MEDLINE | ID: mdl-20125158

ABSTRACT

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.


Subject(s)
Anticoagulants/pharmacology , Melanoma, Experimental/blood supply , Nadroparin/pharmacology , Neovascularization, Pathologic/prevention & control , Pancreatic Neoplasms/blood supply , Skin Neoplasms/prevention & control , Animals , Blood Flow Velocity/drug effects , Cricetinae , Erythrocytes/drug effects , Immunoenzyme Techniques , Mesocricetus , Microcirculation/drug effects
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