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Adv Drug Deliv Rev. 2014 Dec 15;79-80:30-9. doi: 10.1016/j.addr.2014.05.006. Epub 2014 May 9.

Tissue-engineered 3D tumor angiogenesis models: potential technologies for anti-cancer drug discovery.

Author information

1
Leibniz-Institute für Polymerforschung Dresden e.V., Max Bergmann Center of Biomaterials Dresden, Hohe Str. 6, 01069 Dresden, Germany; Technische Universität Dresden, Center for Regenerative Therapies Dresden, Fetscherstr. 105, 01307 Dresden, Germany.
2
Leibniz-Institute für Polymerforschung Dresden e.V., Max Bergmann Center of Biomaterials Dresden, Hohe Str. 6, 01069 Dresden, Germany; Technische Universität Dresden, Center for Regenerative Therapies Dresden, Fetscherstr. 105, 01307 Dresden, Germany. Electronic address: werner@ipfdd.de.

Abstract

Angiogenesis is indispensable for solid tumor expansion, and thus it has become a major target of cancer research and anti-cancer therapies. Deciphering the arcane actions of various cell populations during tumor angiogenesis requires sophisticated research models, which could capture the dynamics and complexity of the process. There is a continuous need for improvement of existing research models, which engages interdisciplinary approaches of tissue engineering with life sciences. Tireless efforts to develop a new model to study tumor angiogenesis result in innovative solutions, which bring us one step closer to decipher the dubious nature of cancer. This review aims to overview the recent developments, current limitations and future challenges in three-dimensional tissue-engineered models for the study of tumor angiogenesis and for the purpose of elucidating novel targets aimed at anti-cancer drug discovery.

KEYWORDS:

Biomaterials; Cancer; Combretastatin (PubChem CID: 335929); Endostatin (PubChem CID: 71581480); Endothelial cells; GM6001 (PubChem CID: 132519); LY294002 (PubChem CID: 3973); Matrix; Microfluidics; PI-103 (PubChem CID: 9884685); SU5416 (PubChem CID: 5329098); SU6668 (PubChem CID: 5329099); Scaffold; Sunitinib (PubChem CID: 5329102); Taxol (PubChem CID: 36314); Thalidomide (PubChem CID: 5426); Vascularization

PMID:
24819220
DOI:
10.1016/j.addr.2014.05.006
[Indexed for MEDLINE]

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