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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Transient inflammatory response induced by apoptotic cells is an important mediator of melanoma cell engraftment and growth

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Author(s):
Correa, Mariangela ; Machado Junior, Joel ; Carneiro, Célia R. W. ; Pesquero, João Bosco ; Bader, Michael ; Chammas, Roger ; Travassos, Luiz Rodolpho Raja Gabaglia [7]
Total Authors: 7
Document type: Journal article
Source: International Journal of Cancer; v. 114, n. 3, p. 356-363, Apr. 2005.
Field of knowledge: Biological Sciences - Immunology
Abstract

Two murine melanoma cell lines, Tm1 and Tm5, were derived from a nontumorigenic lineage of pigmented murine melanocytes, melan-a. Both Tm1 and Tm5 are invariably tumorigenic in syngeneic mice when inoculated s.c. in doses higher than 104 cells; 103 or fewer cells rarely give rise to tumors. We demonstrate that subtumorigenic inocula of Tm1 or Tm5 cells (103) as well as of a known murine melanoma cell line (B16F10) develop as vigorously growing tumor grafts only when coinoculated with apoptotic, but not necrotic cells. The presence of apoptotic cells correlates with a transient inflammatory infiltrate, composed mainly of neutrophils and macrophages. Kinin B1 receptor-deficient mice, which have impaired transmigration of neutrophils to inflamed tissues, had significant growth inhibition of subtumorigenic doses of melanoma cells coinjected with apoptotic cells. Using the same model, tumor take in athymic mice was similar to that seen in wild-type mice, suggesting that a T cell-dependent inflammatory response is not necessary to promote the survival and growth of subtumorigenic doses of melanoma cells. Taken together, our results describe how tumor engraftment and growth can be profoundly affected by microenvironmental alterations in response to the presence of apoptotic cells. Disrupting the delicate balance between apoptotic cells and leukocyte infiltration may provide potentially important insights for understanding and interfering with tumor cell viability during treatment with either -radiation or apoptosis-inducing drugs. (AU)

FAPESP's process: 98/05505-1 - Immune response and immunoprotection against experimental tumors: murine melanoma model
Grantee:Luiz Rodolpho Raja Gabaglia Travassos
Support Opportunities: Research Projects - Thematic Grants