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. Author manuscript; available in PMC: 2017 Aug 30.
Published in final edited form as: Nat Rev Cancer. 2016 Nov 11;17(1):20–37. doi: 10.1038/nrc.2016.108

Figure 4. Nanoparticle targeting of the tumour microenvironment and the premetastatic niche.

Figure 4

Targeting of the tumour vasculature or stromal cells in the tumour microenvironment (part a) and the premetastatic microenvironments such as the bone marrow niche, where induction of the osteogenic differentiation of mesenchymal stem cells enhances bone strength and volume (part b). Cell-specific targeting can be achieved via the modification of nanoparticles (NPs) with ligands that bind to specific receptors (for example, αvβ3 integrin and mannose receptor) on the surface of tumour endothelial cells, stromal cells or other target cells. It should be noted that even without targeting ligands, NPs can be engineered for preferential cellular uptake. The payloads released from NPs localized in tumours or premetastatic tissues can also be nonspecifically taken up by these cells.