2019
DOI: 10.21873/invivo.11592
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Finasteride Enhances Stem Cell Signals of Human Dermal Papilla Cells

Abstract: Background/Aim: Finasteride (FN) has been widely used to treat androgenetic alopecia (AGA). This study aimed at exploring the effect of FN on DP stem cell properties. Materials and Methods: Effect of FN on stem cell properties was tested in a DP cell line and 2 human primary DP cells (HDPCs1 and HDPCs2). Cell toxicity and growth were analyzed by 3-(4,5-dimethylthiazol-2-yl)-2,5diphenyltetrazolium bromide (MTT) assay. The aggregation behavior was observed by phase-contrast microscopy and a scanning electron mic… Show more

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Cited by 15 publications
(11 citation statements)
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“…As shown in Figure 5 , PPE at 0.04mg/mL reduced the activity of the 5α-reductase by 65% in HFDPC, after stimulation by testosterone. This effect was similar to that obtained by finasteride, used as a positive control (Rattanachitthawat et al, 2019 ).…”
Section: Resultssupporting
confidence: 87%
“…As shown in Figure 5 , PPE at 0.04mg/mL reduced the activity of the 5α-reductase by 65% in HFDPC, after stimulation by testosterone. This effect was similar to that obtained by finasteride, used as a positive control (Rattanachitthawat et al, 2019 ).…”
Section: Resultssupporting
confidence: 87%
“…As shown in Figure 5 , PPE at 0.04mg/mL reduced the activity of the 5α-Reductase by 65% in Human Follicle Dermal Papilla cells (HFDPC), after stimulation by testosterone. This effect was similar to that obtained by finasteride, used as positive control 54 .…”
Section: Resultssupporting
confidence: 85%
“…To investigate on the capacity of CeCCE to modulate sebum production in skin cells, the 5α‐R activity was first induced in human dermal fibroblasts by testosterone 100 nM. Then the cells were treated with CeCCE at two concentrations and with the compound (5α,17β)‐(1,1‐Dimethylethyl)‐3‐oxo‐4‐azaandrost‐1‐ene‐17‐carboxamide, a 5α‐R inhibitor, known as Finasteride (Rattanachitthawat, Pinkhien, Opanasopit, Ngawhirunpat, & Chanvorachote, 2019), as a positive control. Significant inhibition of the testosterone‐induced enzymatic activity was produced by CeCCE 0.002% (52.2%) and 0.01% (44.5%), even stronger than those obtained with finasteride (Figure 1).…”
Section: Resultsmentioning
confidence: 99%