Selective Progesterone Receptor Modulator Asoprisnil (J867) Inhibits Proliferation and Induces Apoptosis in Cultured Uterine Leiomyoma Cells But Not in Cultured Normal Myometrial Cells

2005 ◽  
Vol 84 ◽  
pp. S152 ◽  
Author(s):  
W. Chen
2007 ◽  
Vol 293 (4) ◽  
pp. E1002-E1011 ◽  
Author(s):  
Qin Xu ◽  
Noriyuki Ohara ◽  
Jin Liu ◽  
Koji Nakabayashi ◽  
Deborah DeManno ◽  
...  

A recent clinical trial (Chwalisz K, Larsen L, Mattia-Goldberg C, Edmonds A, Elger W, Winkel CA. Fertil Steril 87: 1399–1412, 2007) has demonstrated that the selective progesterone receptor modulator asoprisnil efficiently causes the shrinkage of uterine leiomyoma. The present study was conducted to examine whether asoprisnil elicits endoplasmic reticulum (ER) stress-induced apoptosis in cultured human uterine leiomyoma cells. After subculture in phenol red-free DMEM supplemented with 10% FBS for 120 h, cultured cells were stepped down to serum-free conditions with or without graded concentrations of asoprisnil. ER stress-associated and apoptosis-related proteins were assessed by reverse transcription-PCR analysis or Western blot analysis. RNA interference of growth-arrest- and DNA-damage-inducible gene 153 ( GADD153) was performed using small interfering RNA. Terminal deoxynucleotidyl transferase-mediated 2′-deoxyuridine 5′-triphosphate nick end labeling (TUNEL)-positive rates were assessed by TUNEL assay. Compared with untreated control cultures, treatment with 10−7 M asoprisnil significantly ( P < 0.05) increased the protein contents of ubiquitin at 2 h and phospho-double-stranded RNA-activated protein kinase-like ER kinase, phospho-eukaryotic initiation factor 2α, activating transcription factor 4, and glucose-regulated protein 78 kDa at 4 h, followed by the significant ( P < 0.05) increase in GADD153 protein content at 6 h and cleaved poly(adenosine 5′-diphosphate ribose)polymerase (PARP) at 8 h. RNA interference of GADD153 suppressed protein contents of asoprisnil-induced cleaved PARP, Bax, Bak, GADD34, and tribbles-related protein 3 (TRB3) and TUNEL-positive rate but attenuated asoprisnil-induced reduction in Bcl-2 protein content in cultured leiomyoma cells. These results suggest that asoprisnil elicits ER stress-induced apoptosis in cultured leiomyoma cells and that GADD153 plays a role in asoprisnil-induced apoptosis by modulating the Bcl-2 family of proteins, GADD34, and TRB3.


2006 ◽  
Vol 21 (7) ◽  
pp. 1869-1877 ◽  
Author(s):  
Jiayin Wang ◽  
Noriyuki Ohara ◽  
Zhuo Wang ◽  
Wei Chen ◽  
Akira Morikawa ◽  
...  

2006 ◽  
Vol 92 (2) ◽  
pp. 616-623 ◽  
Author(s):  
Hiroko Sasaki ◽  
Noriyuki Ohara ◽  
Qin Xu ◽  
Jiayin Wang ◽  
Deborah A. DeManno ◽  
...  

Abstract Context: We previously demonstrated that asoprisnil, a selective progesterone receptor modulator, induces apoptosis of cultured uterine leiomyoma cells. This study was conducted to evaluate whether asoprisnil activates TNF-related apoptosis-inducing ligand (TRAIL)-mediated apoptotic pathway in cultured uterine leiomyoma and matching myometrial cells. Objective and Methods: After subculture in phenol red-free DMEM supplemented with 10% fetal bovine serum for 120 h, cultured cells were stepped down to serum-free conditions for 24 h in the absence or presence of graded concentrations of asoprisnil. The levels of TRAIL signaling molecules and cellular inhibitors of apoptosis protein were assessed by Western blot analysis. Results: TRAIL contents in untreated cultured leiomyoma cells were significantly (P &lt; 0.01) lower compared with those in untreated cultured myometrial cells. There was no difference in death receptor (DR)4 and DR5 contents between the two types of cells. Asoprisnil treatment significantly (P &lt; 0.05) increased TRAIL, DR4, and DR5 contents in cultured leiomyoma cells in a dose-dependent manner with a cleavage of caspase-8, -7, and -3, and decreased X-linked chromosome-linked inhibitor of apoptosis protein contents. In cultured myometrial cells, however, asoprisnil treatment did not affect either TRAIL signaling molecule or cellular inhibitors of apoptosis protein contents. The concomitant treatment with 100 ng/ml P4 significantly (P &lt; 0.05) reversed asoprisnil-induced increase in DR4 and cleaved poly(adenosine 5′-diphosphate-ribose) polymerase contents in cultured leiomyoma cells. Conclusions: These results suggest that asoprisnil induces apoptosis of cultured leiomyoma cells by activating TRAIL-mediated apoptotic pathway and down-regulating X-linked chromosome-linked inhibitor of apoptosis protein levels in the absence of comparable effects on myometrial cells.


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