4.6 Review

VEGF-targeted cancer therapy strategies: current progress, hurdles and future prospects

Journal

TRENDS IN MOLECULAR MEDICINE
Volume 13, Issue 6, Pages 223-230

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.molmed.2007.04.001

Keywords

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Funding

  1. NCI NIH HHS [R21-CA117079, R21 CA099237, R21-CA099237, P01-CA80124, R01 CA115767, R21 CA117079, P01 CA080124-08, R21 CA099237-02, P01 CA080124, R01-CA115767, R21 CA117079-02, R01 CA115767-03] Funding Source: Medline

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Despite setbacks, the clinical development of antiangiogenic agents has accelerated remarkably over the past 3-4 years. Consequently, there are currently three direct inhibitors of the VEGF pathway approved for use in cancer therapy. Other agents that block the VEGF pathway are in advanced stages of clinical development and have shown promising results. With these exciting developments come crucial questions regarding the use of these new molecular-targeted agents, alone or in combination with standard cytotoxic or targeted agents. Importantly, the mechanisms of action of anti-VEGF therapy remain unknown. Here, we discuss several potential mechanisms of action such as tumor vascular normalization, bone marrow-derived cell recruitment blockade and cytostatic effects of anti-VEGF therapy. We review the current progress, the major stumbling blocks and the future directions for anti-cancer therapy using anti-VEGF agents, emphasizing clarification of the underlying molecular mechanisms of action and biomarker identification and validation.

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