1997
DOI: 10.1006/excr.1997.3525
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Induction of Smooth Muscle Cell Phenotype in Cultured Human Prostatic Stromal Cells

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Cited by 118 publications
(103 citation statements)
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References 29 publications
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“…Co-encapsulation of drugs in nanocarriers constitutes a promising approach for tumor drug delivery of fixed drug ratios aiming at achieving higher efficacy and reduced side effects [1,2]. Materials and methods: In vitro quantitative evaluation of combinations with conventional and innovative drugs, at different ratios and in free or nano-encapsulated form, was performed and cytotoxicity assessed by the resazurin assay [3]. Determination of synergism, additivity or antagonism, against the HRPC PC-3 cell line, was performed by the median effect analysis [4].…”
Section: Pp58mentioning
confidence: 99%
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“…Co-encapsulation of drugs in nanocarriers constitutes a promising approach for tumor drug delivery of fixed drug ratios aiming at achieving higher efficacy and reduced side effects [1,2]. Materials and methods: In vitro quantitative evaluation of combinations with conventional and innovative drugs, at different ratios and in free or nano-encapsulated form, was performed and cytotoxicity assessed by the resazurin assay [3]. Determination of synergism, additivity or antagonism, against the HRPC PC-3 cell line, was performed by the median effect analysis [4].…”
Section: Pp58mentioning
confidence: 99%
“…TGFß has been intensely studied, the factor is pleiotropic and its function defined by organ-and cell-type. In prostate, TGFß has been implicated in smooth muscle differentiation [3,4]. Prostates from one day old rats were removed and separated into individual lobes.…”
Section: Pp75mentioning
confidence: 99%
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“…Prostatic tissues were obtained from radical prostatectomy or open prostatectomy specimens and processed for cell culture as previously described (Peehl 1992, Peehl & Sellers 1997. The remainder of the prostate was fixed and serially sectioned.…”
Section: Primary Cell Culturesmentioning
confidence: 99%
“…Non-specific binding was blocked with 10% horse serum, then the cells were incubated with a polyclonal rabbit antiserum against IGFBP-3 (1:400) (Diagnostic Systems). Binding of the primary antibody was detected with biotinylated antirabbit IgG, the avidin-biotin complex reagent, and the substrate diaminobenzidine as previously described (Peehl & Sellers 1997).…”
Section: Immunocytochemistrymentioning
confidence: 99%