| Autor: |
Sipkins DA; Lucas MRS Research Center, Department of Radiology, Stanford University School of Medicine, California 94305, USA., Cheresh DA, Kazemi MR, Nevin LM, Bednarski MD, Li KC |
| Jazyk: |
angličtina |
| Zdroj: |
Nature medicine [Nat Med] 1998 May; Vol. 4 (5), pp. 623-6. |
| DOI: |
10.1038/nm0598-623 |
| Abstrakt: |
Angiogenesis, the formation of new blood vessels, is a requirement for malignant tumor growth and metastasis. In the absence of angiogenesis, local tumor expansion is suppressed at a few millimeters and cells lack routes for distant hematogenous spread. Clinical studies have demonstrated that the degree of angiogenesis is correlated with the malignant potential of several cancers, including breast cancer and malignant melanoma. Moreover, the expression of a specific angiogenesis marker, the endothelial integrin alphaVbeta3, has been shown to correlate with tumor grade. However, studies of tumor angiogenesis such as these have generally relied on invasive procedures, adequate tissue sampling and meticulous estimation of histologic microvessel density. In the present report, we describe a novel approach to detecting angiogenesis in vivo using magnetic resonance imaging (MRI) and a paramagnetic contrast agent targeted to endothelial alphaVbeta3 via the LM609 monoclonal antibody. This approach provided enhanced and detailed imaging of rabbit carcinomas by directly targeting paramagnetic agents to the angiogenic vasculature. In addition, angiogenic 'hot spots' not seen by standard MRI were detected. Our strategy for MR imaging of alphaVbeta3 thus represents a non-invasive means to assess the growth and malignant phenotype of tumors. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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