Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3346368 | Current Opinion in Immunology | 2008 | 6 Pages |
Abstract
Cells of the innate immune system sense tissue damage recognizing in the extracellular environment bona fide intracellular moieties, like high mobility group box 1 (HMGB1). In the case of tumors, HMGB1 recognition has a paradoxical dual effect: it promotes tumor neoangiogenesis and triggers protective anti-neoplastic T-cell responses. Recent advances in the study of HMGB1 have identified candidate molecular mechanisms underlying these apparently contrasting outcomes. A surprising role for innate receptors, including toll like receptor 4 (TLR4), in the response to conventional cancer radio and chemotherapy has also recently emerged, providing new insight into the mechanisms by which these treatments actually work.
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Authors
Lara Campana, Lidia Bosurgi, Patrizia Rovere-Querini,