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Liarozole inhibits transforming growth factor-ß3–mediated extracellular matrix formation in human three-dimensional leiomyoma cultures
Oleh:
Levy, Gary
;
Malik, Minnie
;
Britten, Joy
;
Gilden, Melissa
;
Segars, James
Jenis:
Article from Journal - ilmiah internasional
Dalam koleksi:
Fertility and Sterility (keterangan: ada di ClinicalKey) vol. 102 no. 01 (Jul. 2014)
,
page 272–281.
Topik:
Extracellular matrix
;
liarozole
;
leiomyoma
;
three-dimensional model
;
transforming growth factor-beta
Ketersediaan
Perpustakaan FK
Nomor Panggil:
F02.K.2014.02
Non-tandon:
1 (dapat dipinjam: 0)
Tandon:
tidak ada
Lihat Detail Induk
Isi artikel
Objective To investigate the impact of liarozole on transforming growth factor-ß3 (TGF-ß3) expression, TGF-ß3 controlled profibrotic cytokines, and extracellular matrix formation in a three-dimensional (3D) leiomyoma model system. Design Molecular and immunohistochemical analysis in a cell line evaluated in a three-dimensional culture. Setting Laboratory study. Patient(s) None. Intervention(s) Treatment of leiomyoma and myometrial cells with liarozole and TGF-ß3 in a three-dimensional culture system. Main Outcome Measure(s) Quantitative real-time reverse-transcriptase polymerase chain reaction and Western blotting to assess fold gene and protein expression of TGF-ß3 and TGF-ß3 regulated fibrotic cytokines: collagen 1A1 (COL1A1), fibronectin, and versican before and after treatment with liarozole, and confirmatory immunohistochemical stains of treated three-dimensional cultures. Result(s) Both TGF-ß3 gene and protein expression were elevated in leiomyoma cells compared with myometrium in two-dimensional and 3D cultures. Treatment with liarozole decreased TGF-ß3 gene and protein expression. Extracellular matrix components versican, COL1A1, and fibronectin were also decreased by liarozole treatment in 3D cultures. Treatment of 3D cultures with TGF-ß3 increased gene expression and protein production of COL1A1, fibronectin, and versican. Conclusion(s) Liarozole decreased TGF-ß3 and TGF-ß3–mediated extracellular matrix expression in a 3D uterine leiomyoma culture system.
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