Published August 15, 2011 | Version v1
Journal article

Therapeutic Approaches to Target Cancer Stem Cells

  • 1. Department of Systems Biology, Center of Molecular Immunology, 216 Street, PO Box 16040, Atabey, Havana 11600 (Cuba)

Description

The clinical relevance of cancer stem cells (CSC) remains a major challenge for current cancer therapies, but preliminary findings indicate that specific targeting may be possible. Recent studies have shown that these tumor subpopulations promote tumor angiogenesis through the increased production of VEGF, whereas the VEGF neutralizing antibody bevacizumab specifically inhibits CSC growth. Moreover, nimotuzumab, a monoclonal antibody against the epidermal growth factor receptor (EGFR) with a potent antiangiogenic activity, has been shown by our group to reduce the frequency of CSC-like subpopulations in mouse models of brain tumors when combined with ionizing radiation. These studies and subsequent reports from other groups support the relevance of approaches based on molecular-targeted therapies to selectively attack CSC. This review discusses the relevance of targeting both the EGFR and angiogenic pathways as valid approaches to this aim. We discuss the relevance of identifying better molecular markers to develop drug screening strategies that selectively target CSC

Availability note (English)

Available from http://dx.doi.org/10.3390/cancers3033331; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759198

Additional details

Publishing Information

Journal Title
Cancers (Basel)
Journal Volume
3
Journal Issue
3
Journal Page Range
p. 3331-3352
ISSN
2072-6694

INIS

Country of Publication
Switzerland
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
47001794
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
ANGIOGENESIS; GROWTH FACTORS; MONOCLONAL ANTIBODIES; NEOPLASMS; STEM CELLS; THERAPY
Descriptors DEC
ANIMAL CELLS; ANTIBODIES; DISEASES; MEDICINE; MITOGENS; ORGANIC COMPOUNDS; PROTEINS; SOMATIC CELLS

Optional Information

Copyright
Copyright (c) 2011 by the authors
Notes
PMCID: PMC3759198; PMID: 24212957; PUBLISHER-ID: cancers-03-03331; OAI: oai:pubmedcentral.nih.gov:3759198; licensee MDPI, Basel, Switzerland.; This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).