Abstract
Tumour vasculature targeting has been a very active area of cancer drug discovery over the last decade. Growth of solid tumours beyond a certain point requires a sufficient blood supply in order for them to develop and metastasise. While novel anti-angiogenic and vascular disrupting agents represent an important contribution to the armoury of anti-cancer agents they nevertheless usually require combination with standard cytotoxic therapy in order to demonstrate positive clinical outcomes. In line with this consensus, a new concept has arisen, namely the design of functional hybrids where at least one component of the design targets a tumour angiogenic/vasculature pathway. This review will outline examples of such hybrid/conjugate-based approaches. Emphasis will be placed on their preclinical evaluation with particular focus on the RGD/NGR-conjugates, heparin-related hybrids and antibody-drug conjugates. In conclusion, the benefits and shortcomings of hybrids under development will be discussed in the context of future directions and applications.
| Original language | English |
|---|---|
| Pages (from-to) | 503-524 |
| Number of pages | 22 |
| Journal | Angiogenesis |
| Volume | 16 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - Jul 2013 |
| Externally published | Yes |
Keywords
- Angiogenesis
- Combination therapy
- Conjugates
- Hybrids
- Tumour vasculature
- Vascular disrupting agents