Endothelial Progenitor Cells in Tumor Angiogenesis: Another Brick in the Wall

Author(s)

Marcola, Marina ; Rodrigues, Camila Eleuterio

• Document type: Journal article
• Source: STEM CELLS INTERNATIONAL; v. 2015, p. 10-pg., 2015-01-01.

Abstract

Until 15 years ago, vasculogenesis, the formation of new blood vessels from undifferentiated cells, was thought to occur only during embryonic development. The discovery of circulating cells that are able to promote vascular regeneration and repair-the so-called endothelial progenitor cells (EPCs)-changed that, and EPCs have since been studied extensively. It is already known that EPCs include many subtypes of cells that play a variety of roles in promoting vascular growth. Some EPCs are destined to differentiate into endothelial cells, whereas others are capable of promoting and sustaining angiogenesis through paracrine mechanisms. Vasculogenesis and angiogenesis might constitute complementary mechanisms for postnatal neovascularization, and EPCs could be at the core of this process. Although the formation of new blood vessels from preexisting vasculature plays a beneficial role in many physiological processes, such as wound healing, it also contributes to tumor growth and metastasis. However, many aspects of the role played by EPCs in tumor angiogenesis remain unclear. This review aims to address the main aspects of EPCs differentiation and certain characteristics of their main function, especially in tumor angiogenesis, as well as the potential clinical applications. (AU)

• FAPESP's process: 11/01304-8 - Effect of melatonin on the subpopulations of cultured endothilial cells
• Grantee: Marina Marçola Pereira de Freitas
• Support Opportunities: Scholarships in Brazil - Doctorate