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Bone marrow-derived endothelial progenitor cells contribute to the angiogenic switch in tumor growth and metastatic progression
Authors:Dingcheng Gao  Daniel Nolan  Kevin McDonnell  Linda Vahdat  Robert Benezra  Nasser Altorki  Vivek Mittal
Institution:1. Department of Cardiothoracic Surgery, Lehman Brothers Lung Cancer Research Center, Cornell University Medical Center, 1300 York Avenue, 525 East 68th Street, New York, NY 10065, USA;2. Department of Cell and Developmental Biology, Cornell University Medical Center, 1300 York Avenue, 525 East 68th Street, New York, NY 10065, USA;3. Howard Hughes Medical Institute, Department of Genetic Medicine, Cornell University Medical College, 1300 York Avenue, New York, NY 10065, USA;4. Breast Cancer Research Program, Weill Cornell Breast Cancer, Weill Cornell Medical College, 425 East 61st Street, New York, NY 10065, USA;5. Cancer Biology and Genetics Program, Memorial Sloan-Kettering Cancer Center, Box 241, 1275 York Avenue, New York, NY 10065, USA
Abstract:Emerging evidence indicates that bone marrow (BM)-derived endothelial progenitor cells (EPCs) contribute to angiogenesis-mediated growth of certain tumors in mice and human. EPCs regulate the angiogenic switch via paracrine secretion of proangiogenic growth factors and by direct luminal incorporation into sprouting nascent vessels. While the contributions of EPCs to neovessel formation in spontaneous and transplanted tumors and to the metastatic transition have been reported to be relatively low, remarkably, specific EPC ablation in vivo has resulted in severe angiogenesis inhibition and impaired primary and metastatic tumor growth. The existence of a BM reservoir of EPCs, and the selective involvement of EPCs in neovascularization, have attracted considerable interest because these cells represent novel target for therapeutic intervention. In addition, EPCs are also being used as pharmacodynamic surrogate markers for monitoring cancer progression, as well as for optimizing efficacy of anti-angiogenic therapies in the clinic. This review will focus primarily on recent advances and emerging concepts in the field of EPC biology and discuss ongoing debates involving the role of EPCs in tumor neovascularization. For detailed information on the in vitro characterization of EPCs contribution to non-tumor pathologies, the reader is directed towards several excellent reviews and publications F. Bertolini, Y. Shaked, P. Mancuso and R.S. Kerbel, Nat. Rev., Cancer 6 (2006) 835–845. 1]] J.M. Hill, T. Finkel and A.A. Quyyumi, Vox Sang. 87 Suppl 2 (2004) 31–37. 2]] A.Y. Khakoo and T. Finkel, Annu. Rev. Med. 56 (2005) 79–101. 3]] H.G. Kopp, C.A. Ramos and S. Rafii, Curr. Opin. Hematol. 13 (2006) 175–181. 4]; K.K. Hirschi, D.A. Ingram and M.C. Yoder, Arterioscler. Thromb. Vasc. Biol. 28 (2008) 1584–1595. 5]; F. Timmermans, J. Plum, M.C. Yoder, D.A. Ingram, B. Vandekerckhove and J. Case, J. Cell. Mol. Med. 13 (2009) 87–102. 6]] and reviews by Bertolini, Voest and Yoder in this issue.
Keywords:Bone marrow  EPCs  HSCs  Chemotherapy  Bone marrow transaplantation  Metastasis  Angiogenesis
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