Anti-angiogenesis and metastasis: a tumour and stromal cell alliance

L Moserle1, O Casanovas

  • 1Tumor Angiogenesis Group, Catalan Institute of Oncology - IDIBELL, Spain.

Insights

Tumour progression relies on angiogenesis, driven by tumour and stromal cells. Targeting this process, along with the tumour-stromal alliance, is crucial for effective cancer therapies.

Area of Science:

  • Oncology
  • Cancer Biology
  • Tumour Microenvironment

Background:

  • Tumour progression necessitates an angiogenic program orchestrated by both tumour and stromal cells.
  • Antiangiogenic therapies, while impacting tumour growth, may promote invasion and metastasis.
  • The tumour microenvironment, particularly stromal cells, significantly influences tumour aggressiveness and treatment response.

Purpose of the Study:

  • To investigate the role of the tumour-stromal cell alliance in tumour progression.
  • To highlight the impact of antiangiogenic therapies on tumour invasiveness.
  • To emphasize the need for therapeutic strategies targeting both tumour and stromal components.

Main Methods:

  • Review of preclinical studies on antiangiogenic treatments.
  • Analysis of factors contributing to tumour cell escape.
  • Examination of the tumour-stromal interaction in cancer aggressiveness.

Main Results:

  • Preclinical data indicate a proinvasive/metastatic effect of antiangiogenic treatments.
  • Stromal cells contribute to tumour aggressiveness and mediate short-term effects of antivascular endothelial growth factor therapy.
  • Hypoxia-dependent and -independent factors drive tumour cell escape by altering tumour and stromal cells.

Conclusions:

  • The tumour-stromal cell alliance is a critical factor in tumour progression and metastasis.
  • Targeting angiogenesis alone may have limited long-term efficacy and could promote invasiveness.
  • Innovative therapeutic strategies must consider the dual targeting of tumour and stromal cells to improve clinical outcomes in cancer patients.

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