Angiogenesis has long been accepted as a vital process in the growth and metastasis of tumors. As a result it is the target of several novel anti-cancer medications. Consequently, there is an urgent clinical need to develop accurate, non-invasive imaging techniques to improve the characterization of tumor angiogenesis and the monitoring of the response to anti-angiogenic therapy. Macromolecular MR contrast media (MMCM) offer this diagnostic potential by preferentially exploiting the inherent hyperpermeable nature of new tumor vessels compared with normal vessels. Over the last 10-15 years many classes of MMCM have been developed. When evaluated with dynamic contrast enhanced (DCE) MRI, a number of MMCM have demonstrated in vivo imaging properties that correlate with ex vivo histological features of angiogenesis. The enhancement patterns with some MMCM have been reported to correlate with tumor grade, as well as show response to anti-angiogenic and anti-vascular drugs. Future applications of MMCM include targeted angiogenesis imaging and drug delivery of anti-cancer `payloads'. Herein we discuss the best known MMCMs along with their advantages and disadvantages. (C) 2006 Elsevier Ireland Ltd. All rights reserved.
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Univ Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT USA
Univ Utah, Dept Mat Sci & Engn, Salt Lake City, UT 84112 USAUniv Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT USA
Feng, Yi
Jeong, Eun-Kee
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Univ Utah, Dept Radiol, Salt Lake City, UT 84132 USAUniv Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT USA
Jeong, Eun-Kee
Mohs, Aaron M.
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Univ Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT USAUniv Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT USA
Mohs, Aaron M.
Emerson, Lyska
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Univ Utah, Dept Pathol, Salt Lake City, UT USAUniv Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT USA
Emerson, Lyska
Lu, Zheng-Rong
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Univ Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT USAUniv Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT USA
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Univ New S Wales, Australian Ctr Nanomed, Sch Chem Engn, Sydney, NSW 2052, AustraliaUniv New S Wales, Ctr Adv Macromol Design, Sch Chem Engn, Sydney, NSW 2052, Australia
Li, Yang
Beija, Mariana
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Univ New S Wales, Australian Ctr Nanomed, Sch Chem Engn, Sydney, NSW 2052, AustraliaUniv New S Wales, Ctr Adv Macromol Design, Sch Chem Engn, Sydney, NSW 2052, Australia
Beija, Mariana
Laurent, Sophie
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Univ Mons, NMR & Mol Imaging Lab, Dept Gen Organ & Biomed Chem, B-7000 Mons, BelgiumUniv New S Wales, Ctr Adv Macromol Design, Sch Chem Engn, Sydney, NSW 2052, Australia
Laurent, Sophie
vander Elst, Luce
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Univ Mons, NMR & Mol Imaging Lab, Dept Gen Organ & Biomed Chem, B-7000 Mons, BelgiumUniv New S Wales, Ctr Adv Macromol Design, Sch Chem Engn, Sydney, NSW 2052, Australia
vander Elst, Luce
Muller, Robert N.
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Univ Mons, NMR & Mol Imaging Lab, Dept Gen Organ & Biomed Chem, B-7000 Mons, BelgiumUniv New S Wales, Ctr Adv Macromol Design, Sch Chem Engn, Sydney, NSW 2052, Australia
Muller, Robert N.
Duong, Hien T. T.
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Univ New S Wales, Australian Ctr Nanomed, Sch Chem Engn, Sydney, NSW 2052, AustraliaUniv New S Wales, Ctr Adv Macromol Design, Sch Chem Engn, Sydney, NSW 2052, Australia
Duong, Hien T. T.
Lowe, Andrew B.
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Univ New S Wales, Ctr Adv Macromol Design, Sch Chem Engn, Sydney, NSW 2052, AustraliaUniv New S Wales, Ctr Adv Macromol Design, Sch Chem Engn, Sydney, NSW 2052, Australia
Lowe, Andrew B.
Davis, Thomas P.
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Univ New S Wales, Australian Ctr Nanomed, Sch Chem Engn, Sydney, NSW 2052, AustraliaUniv New S Wales, Ctr Adv Macromol Design, Sch Chem Engn, Sydney, NSW 2052, Australia
Davis, Thomas P.
Boyer, Cyrille
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Univ New S Wales, Ctr Adv Macromol Design, Sch Chem Engn, Sydney, NSW 2052, Australia
Univ New S Wales, Australian Ctr Nanomed, Sch Chem Engn, Sydney, NSW 2052, AustraliaUniv New S Wales, Ctr Adv Macromol Design, Sch Chem Engn, Sydney, NSW 2052, Australia