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Published on: June 18, 2011

A surrogate marker to monitor angiogenesis at last

Martin Schneider1, Marc Tjwa, Peter Carmeliet

  • 1The Flanders Interuniversity Institute for Biotechnology, the Center for Transgene Technology and Gene Therapy, KULeuven, Leuven, B-3000, Belgium.

Cancer Cell
|January 18, 2005
PubMed

Insights

Circulating endothelial precursor cells (CEPs) levels are genetically determined and can predict the effectiveness of anti-angiogenesis cancer drugs. Monitoring CEPs may help optimize anti-cancer therapy.

Area of Science:

  • Oncology
  • Vascular Biology
  • Biomarker Discovery

Background:

  • The first angiogenesis inhibitor is approved for cancer therapy, but optimizing dosage is challenging due to a lack of reliable tumor angiogenesis markers.
  • Tumor angiogenesis, the formation of new blood vessels to feed tumors, is a critical target in cancer treatment.

Discussion:

  • Shaked et al. demonstrate that circulating endothelial precursor cells (CEPs) levels are genetically predetermined and influenced by angiogenic factors.
  • These CEP levels correlate with the efficacy of angiogenesis inhibitors, suggesting their potential as surrogate markers.
  • The study highlights the role of CEPs in tumor vessel formation and their regulation by angiogenic signaling pathways.

Key Insights:

  • Circulating endothelial precursor cell (CEP) levels are genetically regulated and influenced by angiogenic factors.
  • CEP levels serve as a reliable indicator of tumor angiogenesis and reflect the antitumor effects of angiogenesis inhibitors.
  • This research identifies CEPs as a potential surrogate marker for monitoring and adjusting antiangiogenic therapies.

Outlook:

  • Further validation of CEPs as surrogate markers could lead to personalized antiangiogenic treatment strategies.
  • Monitoring CEP levels may enable clinicians to optimize drug dosage and improve patient outcomes in cancer therapy.
  • This work opens avenues for developing novel diagnostic tools based on CEPs for anti-angiogenesis drug monitoring.