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Prostate ; 77(7): 729-742, 2017 May.
Artículo en Inglés | MEDLINE | ID: mdl-28168724

RESUMEN

BACKGROUND: Previous studies showed that human bone marrow stromal HS-5 cells secreted unidentified factor(s) inducing PCa cell death. Herein, the HS-5-derived factor (HS-5 DF) was characterized and identified. METHODS: Conditioned media from confluent HS-5 cells were collected and modified for biochemical characteristic testing of HS-5 DF. Cell survival was measured by apoptosis assay and live/dead assay. Fibulin-1 was identified from gel electrophoresis and mass spectrometry. The validation of Fibulin-1 as a HS-5 DF was done by immunoprecipitation (IP) and genetic knockdown by CRISPR/Cas9 system. RESULTS: HS-5 DF was trypsin and heat sensitive, but pH stable. The tentative size of the factor fell between 30 kDa and 100 kDa. TGF-ß1 treatment led to a suppression of HS-5 DF activity, a property consistent with bone metastasis in prostate cancer. Examination of TGF-ß1 down regulated proteins led to identification of fibulin-1 as a candidate for the DF. IP of Fibulin-1 from HS-5 CM and CRISPR knockdown of Fibulin-1 showed a significant reduction of HS-5 CM-derived PCa cell death. These results strongly support a role for fibulin-1 in HS-5 bone marrow stromal cell induction of PCa cell death. CONCLUSION: Our data indicate that Fibulin-1 functions as a HS-5 bone marrow stromal cell-derived factor inducing prostate cancer cell death. Prostate 77:729-742, 2017. © 2016 Wiley Periodicals, Inc.


Asunto(s)
Proteínas de Unión al Calcio/metabolismo , Células Madre Mesenquimatosas , Neoplasias de la Próstata , Apoptosis/fisiología , Neoplasias Óseas/metabolismo , Neoplasias Óseas/secundario , Muerte Celular/fisiología , Línea Celular Tumoral , Supervivencia Celular/fisiología , Medios de Cultivo Condicionados/análisis , Medios de Cultivo Condicionados/metabolismo , Humanos , Masculino , Células Madre Mesenquimatosas/metabolismo , Células Madre Mesenquimatosas/patología , Neoplasias de la Próstata/metabolismo , Neoplasias de la Próstata/patología , Factor de Crecimiento Transformador beta1/metabolismo
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