| Autor: |
Jayson GC; Institute of Cancer Sciences, Christie Hospital and University of Manchester, Withington, Manchester M20 4BX, U.K., Miller GJ; †Manchester Institute of Biotechnology and School of Chemistry, University of Manchester, MIB, Princess Street, Manchester M1 7DN, U.K., Hansen SU; †Manchester Institute of Biotechnology and School of Chemistry, University of Manchester, MIB, Princess Street, Manchester M1 7DN, U.K., Barath M; ‡Institute of Chemistry, Centre of Glycomics, Dubravska Cesta 9, 845 38 Bratislava, Slovakia., Gardiner JM; †Manchester Institute of Biotechnology and School of Chemistry, University of Manchester, MIB, Princess Street, Manchester M1 7DN, U.K., Avizienyte E; Institute of Cancer Sciences, Christie Hospital and University of Manchester, Withington, Manchester M20 4BX, U.K. |
| Abstrakt: |
Angiogenesis has emerged as a novel target for anti-cancer therapies through randomized clinical trials that tested the benefit of adding vascular endothelial growth factor (VEGF) inhibitors to conventional cytotoxic therapies. However, despite improvements in the progression-free survival, the benefit in overall survival is modest. Tumour angiogenesis is regulated by a number of angiogenic cytokines. Thus innate or acquired resistance to VEGF inhibitors can be caused, at least in part, through expression of other angiogenic cytokines, including fibroblast growth factor 2 (FGF2), interleukin 8 (IL-8) and stromal-cell-derived factor 1α (SDF-1α), which make tumours insensitive to VEGF signalling pathway inhibition. The majority of angiogenic cytokines, including VEGF-A, FGF2, IL-8 and SDF-1α, manifest an obligate dependence on heparan sulfate (HS) for their biological activity. This mandatory requirement of angiogenic cytokines for HS identifies HS as a potential target for novel anti-angiogenic therapy. Targeting multiple angiogenic cytokines with HS mimetics may represent an opportunity to inhibit tumour angiogenesis more efficiently. Our published studies and unpublished work have demonstrated the feasibility of generating synthetic HS fragments of defined structure with biological activity against a number of angiogenic cytokines. |
