Antiangiogenesis strategies revisited: from starving tumors to alleviating hypoxia

Rakesh K Jain1

  • 1Edwin L. Steele Laboratory for Tumor Biology, Department of Radiation Oncology, Harvard Medical School and Massachusetts General Hospital, 100 Blossom Street, Cox 7, Boston, MA 02114, USA.

Cancer Cell
|December 18, 2014
PubMed

Insights

Antiangiogenic drugs can cause tumor hypoxia, potentially hindering cancer treatment. Strategies to improve tumor oxygenation and blood flow may enhance therapy outcomes for various diseases.

Area of Science:

  • Oncology
  • Vascular Biology
  • Cancer Therapeutics

Background:

  • Antiangiogenic drugs targeting VEGF are approved for cancer treatment.
  • These drugs can induce tumor hypoxia, potentially promoting tumor progression and resistance.
  • Clinical data suggest improved perfusion/oxygenation correlates with better patient survival.

Purpose of the Study:

  • To summarize lessons from antiangiogenic therapy research over the past decade.
  • To propose strategies for improving antiangiogenic therapy outcomes.
  • To address outcomes in both malignant and nonmalignant diseases.

Main Methods:

  • Review of preclinical and clinical studies on antiangiogenic therapy.
  • Analysis of the relationship between antiangiogenic agents, tumor hypoxia, and perfusion.
  • Synthesis of data to inform therapeutic strategies.

Main Results:

  • Antiangiogenic therapy can paradoxically increase tumor hypoxia.
  • Improved tumor perfusion and oxygenation are associated with longer survival.
  • Hypoxia can drive tumor progression and treatment resistance.

Conclusions:

  • Alleviating tumor hypoxia is crucial for enhancing antiangiogenic therapy.
  • Strategies improving perfusion and oxygenation may boost radiotherapy, chemotherapy, and immunotherapy.
  • Optimized antiangiogenic approaches hold promise for treating various diseases.

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