Dienogest inhibits BrdU uptake with G0/G1 arrest in cultured endometriotic stromal cells

Fu Li, Li Fu, Fu L, Osuga Y, Yutaka Osuga, Chieko Morimoto, Morimoto C, Tetsuya Hirata, Yasushi Hirota, Tetsu Yano, Yano T, Yuji Taketani, Taketani Y
Fertility and sterility · 2007 · vol. 89(5) , pp. 1344–1347 · doi:10.1016/j.fertnstert.2007.03.042 · PMID:17511992 · W2128216220
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Dienogest was found to inhibit BrdU uptake and induce G0/G1 cell cycle arrest in cultured endometriotic stromal cells.

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Abstract

OBJECTIVE: To investigate the effect of dienogest on the proliferation of endometriotic stromal cells. DESIGN: Comparative and laboratory study. SETTING: University of Tokyo Hospital. PATIENT(S): Endometriotic stromal cells were isolated and cultured from ovarian endometriomas of patients undergoing surgery. INTERVENTION(S): Dienogest was added to the cultured endometriotic stromal cells. MAIN OUTCOME MEASURE(S): 5-Bromo-2'-deoxyuridine (BrdU) incorporation into DNA of the endometriotic stromal cells was measured by ELISA. Cell cycle analysis of the cultured endometriotic stromal cells was performed by flow cytometry. RESULT(S): Dienogest at concentration of 10(-7) M and 10(-6) M significantly inhibited BrdU incorporation into DNA at 24 and 48 hours. Dienogest significantly increased the cells in G0/G1 phase and reduced the cells in S phase and G2/M phase in 24 and 48 hours. CONCLUSION(S): The present study indicates that dienogest can inhibit the proliferation of the endometriotic stromal cells with G0/G1 arrest, suggesting a possible direct effect of dienogest in the treatment of endometriosis.

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Condition tags

endometriosis

MeSH descriptors

Bromodeoxyuridine Cell Proliferation Endometriosis G1 Phase Nandrolone Ovarian Diseases Resting Phase, Cell Cycle Stromal Cells Adult Adult Bromodeoxyuridine Bromodeoxyuridine Cell Cycle Cell Cycle Cell Cycle Cell Proliferation Cell Proliferation Cells, Cultured Cells, Cultured Contraceptives, Oral

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Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. Outer rings show 2-hop neighbours — papers reached through the immediate citers/citees. [ collapse to 1-hop ]

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