Abstract

Breast cancer is the most common cancer affecting women and is the second leading cause of cancer related death worldwide. Angiogenesis, the process of new blood vessel development from pre-existing vasculature, has been implicated in the growth, progression, and metastasis of cancer. Tumor angiogenesis has been explored as a key therapeutic target for decades, as the blockade of this process holds the potential to reduce the oxygen and nutrient supplies that are required for tumor growth. However, many existing anti-angiogenic approaches, such as those targeting Vascular Endothelial Growth Factor, Notch, and Angiopoietin signaling, have been associated with severe side-effects, limited survival advantage, and enhanced cancer regrowth rates. To address these setbacks, alternative pathways involved in the regulation of tumor angiogenesis are being explored, including those involving Bone Morphogenetic Protein-9 signaling, the Sonic Hedgehog pathway, Cyclooxygenase-2, p38-mitogen-activated protein kinase, and Chemokine Ligand 18. This review article will introduce the concept of tumor angiogenesis in the context of breast cancer, followed by an overview of current anti-angiogenic therapies, associated resistance mechanisms and novel therapeutic targets.

Highlights

  • Breast cancer is the most common invasive cancer affecting women

  • This process has been attributed to the actions of a subset of cancer stem cells that possess a high degree of differentiation plasticity and can acquire a range of endothelial markers, including cluster of differentiation 31 (CD31), Vascular Endothelial Growth Factor (VEGF) receptor-2 (VEGFR2), Tie2, ephrin A2, and VE-Cadherin [53, 54]

  • In addition to this lack of efficacy, long term trials with Bevacizumab concluded that excessive neutralization of VEGF with high doses or prolonged exposure caused vascular regression and promoted hypoxia [84, 85], driving the selection of more invasive cancer cells that can contribute to tumor resistance and increased metastatic potential [84]

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Summary

Novel Pathways for Targeting Tumor Angiogenesis in Metastatic Breast Cancer

Reviewed by: Luis E Arias-Romero, National Autonomous University of Mexico, Mexico Vaishali Aggarwal, University of Pittsburgh, United States. Many existing anti-angiogenic approaches, such as those targeting Vascular Endothelial Growth Factor, Notch, and Angiopoietin signaling, have been associated with severe sideeffects, limited survival advantage, and enhanced cancer regrowth rates. To address these setbacks, alternative pathways involved in the regulation of tumor angiogenesis are being explored, including those involving Bone Morphogenetic Protein-9 signaling, the Sonic Hedgehog pathway, Cyclooxygenase-2, p38-mitogen-activated protein kinase, and Chemokine Ligand 18. This review article will introduce the concept of tumor angiogenesis in the context of breast cancer, followed by an overview of current antiangiogenic therapies, associated resistance mechanisms and novel therapeutic targets.

INTRODUCTION
Novel Pathways Targeting Tumor Angiogenesis
Sprouting Angiogenesis
The Tumor Microenvironment
Vascular Mimicry
VEGF Pathway Inhibitors
Associated Trials
Notch Signaling Pathway
Ang Pathway Inhibitors
THE NEED FOR ALTERNATIVE PATHWAYS FOR BREAST CANCER THERAPEUTICS
Multiple Clinical Trials
Novel Pathways Targeting Tumor Angiogenesis C
Shh Signaling
Novel Pathways Targeting Tumor Angiogenesis B
AUTHOR CONTRIBUTIONS
Full Text
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