Tumor rim cells: From resistance to vascular targeting agents to complete tumor ablation

Khaled Seidi1, Rana Jahanban-Esfahlan1, Nosratollah Zarghami2

  • 11 Department of Medical Biotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.

Insights

Vascular targeting therapies aim to stop tumor growth by cutting off blood supply. This review emphasizes that targeting tumor rim cells is crucial for achieving lasting cancer cures and overcoming treatment resistance.

Area of Science:

  • Oncology
  • Vascular Biology
  • Cancer Therapy

Background:

  • Vascular targeting agents (VTAs) aim to inhibit tumor growth by disrupting blood vessels.
  • Current VTAs include anti-angiogenesis agents and vascular disrupting agents.
  • Despite therapeutic potential, complete tumor eradication and cure remain challenging due to treatment resistance.

Purpose of the Study:

  • To highlight the critical role of tumor rim cells in determining the success of vascular targeting therapies.
  • To review single and combination treatments that target tumor rim cells effectively.
  • To explore strategies for eliminating residual rim cells for permanent tumor ablation.

Main Methods:

  • Literature review of current vascular targeting strategies.
  • Analysis of preclinical and clinical data on tumor recurrence and resistance.
  • Discussion of the biology and survival mechanisms of tumor rim cells.

Main Results:

  • Tumor rim cells are identified as a key factor in the refractoriness of tumors to vascular targeting agents.
  • Specific treatment approaches targeting these rim cells show promise for long-lasting tumor cure.
  • Understanding rim cell behavior is essential for developing more effective therapies.

Conclusions:

  • Targeting tumor rim cells is critical for overcoming resistance and achieving durable responses with vascular targeting agents.
  • Future strategies should focus on eliminating residual rim cells to achieve complete tumor ablation.
  • Further research into the mechanisms of rim cell survival and contribution to refractoriness is warranted.

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