Assuntos
Melanócitos/enzimologia , Proteína Quinase C-alfa/genética , Proteína Quinase C-delta/genética , Proteína Quinase C/genética , Linhagem Celular , Linhagem Celular Tumoral , Regulação Enzimológica da Expressão Gênica , Humanos , Imuno-Histoquímica , Isoenzimas , Melanócitos/citologia , Melanócitos/fisiologia , Melanoma/enzimologia , Melanoma/patologia , Melanoma/fisiopatologia , Proteína Quinase C/análise , Proteína Quinase C/fisiologia , Proteína Quinase C beta , Proteína Quinase C-alfa/análise , Proteína Quinase C-alfa/fisiologia , Proteína Quinase C-delta/análise , Proteína Quinase C-delta/fisiologiaRESUMO
Bone morphogenetic proteins (BMPs) are members of the transforming growth factor-beta (TGF-beta) superfamily serving multiple functions in many cell and tissue types including proliferation, apoptosis, differentiation, chemotaxis, angiogenesis, and matrix production during embryogenic development as well as in adult life. Despite the tremendous progress in delineating functional derangements of BMP pathways in carcinogenesis during the last decade, the biological significance of BMPs in human melanoma has received very little attention. It is now clear that biological responses to BMPs are cell type-specific and divergent effects, i.e., both oncogenic and tumor suppressor activities, have been described. Thus, knowledge generated in one system may not translate directly to another. In this review, we summarize the current understanding of BMP signaling in various human cancers and discuss original data pertaining to cutaneous melanoma obtained in our laboratory.