In pursuit of new anti-angiogenic therapies for cancer treatment.

Front Biosci (Landmark Ed)

Department of Anatomy and Cell Biology, University of Florida, Gainesville, FL 32610, USA.

Published: January 2011

AI Article Synopsis

  • Despite advancements in cancer treatments, patients still face a poor prognosis due to issues like abnormal tumor blood vessel growth (angiogenesis) and cancer spread (metastasis).
  • The initial success of anti-angiogenic drugs targeting the VEGF pathway sparked a search for new treatments, but these drugs have shown limited clinical benefits.
  • Recent research suggests that understanding the unique features of tumor blood vessels and their environment may help create more effective anti-angiogenic therapies by addressing the mechanisms that enable tumors to resist current treatments.

Article Abstract

Despite advances in surgery, radiation therapy, and chemotherapy, patients with cancer have a poor prognosis. Sustained aberrant tumor angiogenesis and metastasis is a major obstacle for effective cancer treatment. Just a few years ago, few would argue that one of the key success stories of the modern cancer medicine were the anti-angiogenic drugs targeting the vascular endothelial growth factor (VEGF) signaling pathway approved by FDA. This initial success inspired many researchers to search for new anti-angiogenic targets and drugs with the hope that one day, anti-angiogenic therapy might really become the panacea for cancer patients. Unfortunately, the limited clinical benefits achieved with anti-angiogenic drugs conflicts with the widely accepted notion that angiogenesis is a key event in tumor progression. Emerging data indicate that unique characteristics of the tumor vasculature within the tumor microenvironment may hold the key for success of anti-angiogenic therapy. In particular, the molecular and cellular alterations that sustain aberrant tumor angiogenesis in the face of angiogenic inhibitors represents novel targets for rationally designing and improving current anti-angiogenic strategies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3627482PMC
http://dx.doi.org/10.2741/3721DOI Listing

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