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Mol Nutr Food Res ; 58(10): 2001-13, 2014 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-25044704

RESUMO

SCOPE: Epidemiological studies provide evidence that consumption of cruciferous vegetables, like broccoli, can reduce the risk of cancer development. Sulforaphane (SFN) is a phytochemical derived from cruciferous vegetables that induces anti-proliferative and pro-apoptotic responses in prostate cancer cells, but not in normal prostate cells. The mechanisms responsible for this cancer-specific cytotoxicity remain unclear. METHODS AND RESULTS: We utilized RNA sequencing and determined the transcriptomes of normal prostate epithelial cells, androgen-dependent prostate cancer cells, and androgen-independent prostate cancer cells treated with SFN. SFN treatment dynamically altered gene expression and resulted in distinct transcriptome profiles depending on prostate cell line. SFN also down-regulated the expression of genes that were up-regulated in prostate cancer cells. Network analysis of genes altered by SFN treatment revealed that the transcription factor Specificity protein 1 (Sp1) was present in an average of 90.5% of networks. Sp1 protein was significantly decreased by SFN treatment in prostate cancer cells and Sp1 may be an important mediator of SFN-induced changes in expression. CONCLUSION: Overall, the data show that SFN alters gene expression differentially in normal and cancer cells with key targets in chemopreventive processes, making it a promising dietary anti-cancer agent.


Assuntos
Anticarcinógenos/farmacologia , Isotiocianatos/farmacologia , Proteínas de Neoplasias/antagonistas & inibidores , Próstata/efeitos dos fármacos , Neoplasias da Próstata/tratamento farmacológico , Fator de Transcrição Sp1/antagonistas & inibidores , Transcriptoma/efeitos dos fármacos , Anticarcinógenos/efeitos adversos , Carcinogênese/efeitos dos fármacos , Linhagem Celular Tumoral , Células Cultivadas , Quimioprevenção , Suplementos Nutricionais/efeitos adversos , Regulação Neoplásica da Expressão Gênica/efeitos dos fármacos , Inativação Gênica , Humanos , Isotiocianatos/efeitos adversos , Masculino , Proteínas de Neoplasias/genética , Proteínas de Neoplasias/metabolismo , Próstata/citologia , Próstata/metabolismo , Neoplasias da Próstata/metabolismo , Neoplasias de Próstata Resistentes à Castração/tratamento farmacológico , Neoplasias de Próstata Resistentes à Castração/metabolismo , RNA Interferente Pequeno , Fator de Transcrição Sp1/genética , Fator de Transcrição Sp1/metabolismo , Sulfóxidos
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