Apoptosis and endometriosis

被引:64
作者
Harada, Tasuku
Taniguchi, Fuminori
Izawa, Masao
Ohama, Yoko
Takenaka, Yasuko
Tagashira, Yukiko
Ikeda, Ayako
Watanabe, Ayako
Iwabe, Tomio
Terakawa, Naoki
机构
[1] Tottori Univ, Sch Med, Dept OB GYN, Yonago, Tottori 6838504, Japan
[2] Tottori Univ, Sch Med, Dept Biosignalling, Yonago, Tottori 6838504, Japan
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2007年 / 12卷
关键词
apoptosis; Bcl-2; endometriosis; Fas; Fasl system; review;
D O I
10.2741/2302
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apoptosis plays a critical role in maintaining tissue homeostasis and represents a normal function to eliminate excess or dysfunctional cells. Accumulated evidence suggest that apoptosis helps to maintain cellular homeostasis during the menstrual cycle by eliminating senescent cells from the functional layer of the uterine endometrium during the late secretory and menstrual phase of the cycle. BCL-2 family and Fas/FasL system have been extensively studied in human endometrium and endometriotic tissues. Eutopic endometrium from women with endometriosis reportedly has some fundamental differences compared with normal endometrium of women without endometriosis. The differences could contribute to the survival of regurgitating endometrial cells into the peritoneal cavity and the development of endometriosis. One mechanism that recently gained a lot of interest is the finding that apoptosis appeared in eutopic and ectopic endometrium of patients with endometriosis. This study is a current review of the literature focused on the physiological role of apoptosis in normal endometrium and the alterations in regulation of apoptosis in eutopic and ectopic endometrium from women with endometriosis. Finally, role of apoptosis in the treatment of endometriosis is reviewed to link the basic research findings into clinical applications.
引用
收藏
页码:3140 / 3151
页数:12
相关论文
共 127 条
[1]  
Aplin AE, 1998, PHARMACOL REV, V50, P197
[2]  
Arimoto T, 2003, INT J ONCOL, V22, P551
[3]   Menstrual characteristics associated with endometriosis [J].
Arumugam, K ;
Lim, JMH .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1997, 104 (08) :948-950
[4]  
Bartelmez GW., 1957, CONTRIB EMBRYOL, V36, P153
[5]   Reduction of apoptosis and proliferation in endometriosis [J].
Béliard, A ;
Noël, A ;
Foidart, JM .
FERTILITY AND STERILITY, 2004, 82 (01) :80-85
[6]   A ROLE FOR CD95 LIGAND IN PREVENTING GRAFT-REJECTION [J].
BELLGRAU, D ;
GOLD, D ;
SELAWRY, H ;
MOORE, J ;
FRANZUSOFF, A ;
DUKE, RC .
NATURE, 1995, 377 (6550) :630-632
[7]  
BILOTAS MA, 2006, IN PRESS HUM REPROD
[8]   BCL-X, A BCL-2-RELATED GENE THAT FUNCTIONS AS A DOMINANT REGULATOR OF APOPTOTIC CELL-DEATH [J].
BOISE, LH ;
GONZALEZGARCIA, M ;
POSTEMA, CE ;
DING, LY ;
LINDSTEN, T ;
TURKA, LA ;
MAO, XH ;
NUNEZ, G ;
THOMPSON, CB .
CELL, 1993, 74 (04) :597-608
[9]  
BRAUN DP, 1992, FERTIL STERIL, V57, P1203
[10]   Cytolysis of eutopic and ectopic endometrial cells by peripheral blood monocytes and peritoneal macrophages in women with endometriosis [J].
Braun, DP ;
Gebel, H ;
Rana, N ;
Dmowski, WP .
FERTILITY AND STERILITY, 1998, 69 (06) :1103-1108