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The Inhibition of Vessel Co-Option as an Emerging Strategy for Cancer Therapy
Iván Carrera-Aguado1,2, Laura Marcos-Zazo1,2, Patricia Carrancio-Salán1,2
1Departamento de Bioquímica y Biología Molecular, Universidad de Salamanca, 37007 Salamanca, Spain.
International Journal of Molecular Sciences
|January 23, 2024
Summary
Vessel co-option (VCO) hijacks existing blood vessels for tumor growth, contributing to therapy resistance. Understanding VCO mechanisms is crucial for developing new anti-cancer strategies.
Area of Science:
- Oncology
- Cell Biology
- Cancer Research
Background:
- Vessel co-option (VCO) is a non-angiogenic tumor vascularization mechanism.
- VCO enables tumors to utilize pre-existing vasculature for nutrients and invasion.
- It is linked to poor prognosis and resistance to anti-angiogenic therapies.
Purpose of the Study:
- To review the cellular and molecular mechanisms underlying VCO.
- To explore potential therapeutic strategies targeting VCO.
- To address the lack of current treatments inhibiting VCO.
Main Methods:
- Literature review of recent studies on VCO.
- Analysis of molecular and cellular processes in VCO.
- Identification of therapeutic targets and strategies.
Main Results:
- Co-opted vessels exhibit a quiescent phenotype, unlike angiogenic vessels.
- Cancer cells adhere to basement membranes via integrins, showing mesenchymal traits.
- The tumor microenvironment, including ECM and immune cells, influences VCO.
Conclusions:
- VCO is a critical factor in tumor progression and therapy resistance.
- Targeting VCO mechanisms offers a potential strategy to overcome anti-angiogenic resistance.
- Further research into VCO inhibition is needed for novel therapeutic development.
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