Targeting tumor-associated macrophages and inhibition of MCP-1 reduce angiogenesis and tumor growth in a human melanoma xenograft
Chemokines such as monocyte chemoattractant protein (MCP)-1 are key agonists that attract macrophages to tumors. In melanoma, it has been previously shown that variable levels of MCP-1/CCL2 appear to correlate with infiltrating macrophages and tumor fate, with low to intermediate levels of the chemo...
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| Autores principales: | , , , , , , , , |
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| Formato: | Articulo |
| Lenguaje: | Inglés |
| Publicado: |
2007
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| Acceso en línea: | http://sedici.unlp.edu.ar/handle/10915/83061 |
| Aporte de: |
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I19-R120-10915-83061 |
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| record_format |
dspace |
| institution |
Universidad Nacional de La Plata |
| institution_str |
I-19 |
| repository_str |
R-120 |
| collection |
SEDICI (UNLP) |
| language |
Inglés |
| topic |
Ciencias Veterinarias Ciencias Médicas melanoma tumor |
| spellingShingle |
Ciencias Veterinarias Ciencias Médicas melanoma tumor Gazzaniga, Silvina Bravo, Alicia I. Guglielmotti, Angelo Van Rooijen, Nico Maschi, Fabricio Alejandro Vecchi, Annunciata Mantovani, Alberto Mordoh, José Wainstok, Rosa Targeting tumor-associated macrophages and inhibition of MCP-1 reduce angiogenesis and tumor growth in a human melanoma xenograft |
| topic_facet |
Ciencias Veterinarias Ciencias Médicas melanoma tumor |
| description |
Chemokines such as monocyte chemoattractant protein (MCP)-1 are key agonists that attract macrophages to tumors. In melanoma, it has been previously shown that variable levels of MCP-1/CCL2 appear to correlate with infiltrating macrophages and tumor fate, with low to intermediate levels of the chemokine contributing to melanoma development. To work under such conditions, a poorly tumorigenic human melanoma cell line was transfected with an expression vector encoding MCP-1. We found that M2 macrophages are associated to MCP-1<SUP>+</SUP> tumors, triggering a profuse vascular network. To target the protumoral macrophages recruitment and reverting tumor growth promotion, clodronate-laden liposomes (Clod-Lip) or bindarit were administered to melanoma-bearing mice. Macrophage depletion after Clod-Lip treatment induced development of smaller tumors than in untreated mice. Immunohistochemical analysis with an anti-CD31 antibody revealed scarce vascular structures mainly characterized by narrow vascular lights. Pharmacological inhibition of MCP-1 with bindarit also reduced tumor growth and macrophage recruitment, rendering necrotic tumor masses. We suggest that bindarit or Clod-Lip abrogates protumoral-associated macrophages in human melanoma xenografts and could be considered as complementary approaches to antiangiogenic therapy. |
| format |
Articulo Articulo |
| author |
Gazzaniga, Silvina Bravo, Alicia I. Guglielmotti, Angelo Van Rooijen, Nico Maschi, Fabricio Alejandro Vecchi, Annunciata Mantovani, Alberto Mordoh, José Wainstok, Rosa |
| author_facet |
Gazzaniga, Silvina Bravo, Alicia I. Guglielmotti, Angelo Van Rooijen, Nico Maschi, Fabricio Alejandro Vecchi, Annunciata Mantovani, Alberto Mordoh, José Wainstok, Rosa |
| author_sort |
Gazzaniga, Silvina |
| title |
Targeting tumor-associated macrophages and inhibition of MCP-1 reduce angiogenesis and tumor growth in a human melanoma xenograft |
| title_short |
Targeting tumor-associated macrophages and inhibition of MCP-1 reduce angiogenesis and tumor growth in a human melanoma xenograft |
| title_full |
Targeting tumor-associated macrophages and inhibition of MCP-1 reduce angiogenesis and tumor growth in a human melanoma xenograft |
| title_fullStr |
Targeting tumor-associated macrophages and inhibition of MCP-1 reduce angiogenesis and tumor growth in a human melanoma xenograft |
| title_full_unstemmed |
Targeting tumor-associated macrophages and inhibition of MCP-1 reduce angiogenesis and tumor growth in a human melanoma xenograft |
| title_sort |
targeting tumor-associated macrophages and inhibition of mcp-1 reduce angiogenesis and tumor growth in a human melanoma xenograft |
| publishDate |
2007 |
| url |
http://sedici.unlp.edu.ar/handle/10915/83061 |
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Repositorios |
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