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Resveratrol Enhances Apoptosis in Endometriotic Stromal Cells.

Authors :
Taguchi, Ayumi
Koga, Kaori
Kawana, Kei
Makabe, Tomoko
Sue, Fusako
Miyashita, Mariko
Yoshida, Mitsuyo
Urata, Yoko
Izumi, Gentaro
Tkamura, Masashi
Harada, Miyuki
Hirata, Tetsuya
Hirota, Yasushi
Wada‐Hiraike, Osamu
Fujii, Tomoyuki
Osuga, Yutaka
Source :
American Journal of Reproductive Immunology; Apr2016, Vol. 75 Issue 4, p486-492, 7p
Publication Year :
2016

Abstract

Problem Resistance to apoptosis, together with inflammatory and invasive activity, contributes to the pathogenesis of endometriosis; therefore, approaches that can safely enhance apoptosis in endometriotic tissue are highly sought after as a means of managing the disease. Although resveratrol ( RVT) is known to induce apoptosis or increase sensitivity to apoptotic stimuli in various cancer cell types, its effect on human endometriosis has remained uncertain. This study aimed to investigate whether RVT induces or enhances apoptosis in human endometriotic stromal cells ( ESCs). Method of study Endometriotic tissues were collected, during laparoscopies, from women affected by ovarian endometriosis. ESCs were prepared, cultured, and treated with RVT. Apoptosis was assessed by annexin V- PI staining. Survivin mRNA expression in ESCs was examined using RT- PCR. ESCs were pre-treated with or without RVT and then incubated with TNF-α-related-apoptosis-inducing ligand ( TRAIL), which is a known pro-apoptotic molecule. Results RVT alone did not induce apoptosis in ESCs. RVT significantly reduced survivin mRNA expression ( P < 0.05). Pre-treatment with RVT significantly enhanced TRAIL-induced apoptosis (8.13 ± 0.83% (control) versus 29.19 ± 7.39% (pre-treated with RVT), P < 0.05). Conclusion This study indicates that RVT suppresses survivin expression and enhances TRAIL-induced apoptosis in ESCs. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10467408
Volume :
75
Issue :
4
Database :
Complementary Index
Journal :
American Journal of Reproductive Immunology
Publication Type :
Academic Journal
Accession number :
113416734
Full Text :
https://doi.org/10.1111/aji.12489