TY - JOUR
T1 - Tumor angiogenesis and progression are enhanced by Sema4D produced by tumor-associated macrophages
AU - Sierra, Jose Rafael
AU - Corso, Simona
AU - Caione, Luisa
AU - Cepero, Virna
AU - Conrotto, Paolo
AU - Cignetti, Alessandro
AU - Piacibello, Wanda
AU - Kumanogoh, Atsushi
AU - Kikutani, Hitoshi
AU - Comoglio, Paolo Maria
AU - Tamagnone, Luca
AU - Giordano, Silvia
PY - 2008
Y1 - 2008
N2 - Increased evidence suggests that cancer-associated infiammation supports tumor growth and progression. We have previously shown that semaphorin 4D (Sema4D), a ligand produced by different cell types, is a proangiogenic molecule that acts by binding to its receptor, plexin B1, expressed on endothelial cells (Conrotto, P., D. Valdembri, S. Corso, G. Serini, L. Tamagnone, P.M. Comoglio, F. Bussolino, and S. Giordano. 2005. Blood. 105:4321 - 4329). The present work highlights the role of Sema4D produced by the tumor microenvironment on neoplastic angiogenesis. We show that in an environment lacking Sema4D, the ability of cancer cells to generate tumor masses and metastases is severely impaired. This condition can be explained by a defective vascularization inside the tumor. We demonstrate that tumor-associated macrophages (TAMs) are the main cells producing Sema4D within the tumor stroma and that their ability to produce Sema4D is critical for tumor angiogenesis and vessel maturation. This study helps to explain the protumoral role of infiammatory cells of the tumor stroma and leads to the identification of an angiogenic molecule that might be a novel therapeutic target.
AB - Increased evidence suggests that cancer-associated infiammation supports tumor growth and progression. We have previously shown that semaphorin 4D (Sema4D), a ligand produced by different cell types, is a proangiogenic molecule that acts by binding to its receptor, plexin B1, expressed on endothelial cells (Conrotto, P., D. Valdembri, S. Corso, G. Serini, L. Tamagnone, P.M. Comoglio, F. Bussolino, and S. Giordano. 2005. Blood. 105:4321 - 4329). The present work highlights the role of Sema4D produced by the tumor microenvironment on neoplastic angiogenesis. We show that in an environment lacking Sema4D, the ability of cancer cells to generate tumor masses and metastases is severely impaired. This condition can be explained by a defective vascularization inside the tumor. We demonstrate that tumor-associated macrophages (TAMs) are the main cells producing Sema4D within the tumor stroma and that their ability to produce Sema4D is critical for tumor angiogenesis and vessel maturation. This study helps to explain the protumoral role of infiammatory cells of the tumor stroma and leads to the identification of an angiogenic molecule that might be a novel therapeutic target.
KW - Immunology
KW - Immunology and Allergy
KW - Immunology
KW - Immunology and Allergy
UR - http://hdl.handle.net/10807/140990
UR - http://www.jem.org/cgi/reprint/205/7/1673
U2 - 10.1084/jem.20072602
DO - 10.1084/jem.20072602
M3 - Article
SN - 0022-1007
VL - 205
SP - 1673
EP - 1685
JO - Journal of Experimental Medicine
JF - Journal of Experimental Medicine
ER -