Proteomic analysis of follicular fluid from women with and without endometriosis: New therapeutic targets and biomarkers

被引:49
作者
Lo Turco, Edson Guimaraes [1 ]
Cordeiro, Fernanda Bertuccez [1 ]
de Carvalho Lopes, Paula Helena [1 ]
Gozzo, Fabio Cesar [2 ]
Pilau, Eduardo Jorge [2 ]
Soler, Thiesa Butterby [1 ]
da Silva, Barbara Ferreira [1 ]
Del Giudice, Paula Toni [1 ]
Bertolla, Ricardo Pimenta [1 ]
Fraietta, Renato [1 ]
Cedenho, Agnaldo Pereira [1 ]
机构
[1] Univ Fed Sao Paulo, Div Urol, Human Reprod Sect, Dept Surg, BR-05012000 Sao Paulo, Brazil
[2] Univ Estadual Campinas, Inst Chem, Campinas, SP, Brazil
关键词
IN-VITRO FERTILIZATION; INTEGRIN EXPRESSION; INFERTILE PATIENTS; MECHANISMS; DIAGNOSIS; QUALITY; EMBRYO; SERUM;
D O I
10.1002/mrd.22180
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Endometriosis is a gynecological disease that affects women of reproductive age. The protein profiles of women with endometriosis who were able or unable to achieve pregnancy and women without endometriosis who did achieve pregnancy were compared in this study. The follicular fluid was collected from 21 patients undergoing in vitro-fertilization treatment, according to the following groups: nine women in the control group (Group C), four women with endometriosis who achieved pregnancy (Group E.P), and eight women with endometriosis who did not achieve pregnancy (Group E.NP). Follicular fluid proteins were separated using 2D-electrophoresis,and their spots were compared, excised, and submitted to LC-ESI-MS/MS for proteins identification. The analysis showed 29 differentially expressed spots among the groups, and from these, 21 proteins were identified. Analysis showed some functional enrichment in the E.P group, including response to oxidative stress and apoptosis, while the E.NP group showed functions related to response to reactive oxygen species and positive regulation of apoptosis. These data suggest that endometriosis leads to differential protein expression in the follicular fluid, which can influences the outcome of pregnancy. These proteins may be potential targets for better diagnostics and new therapeutic intervention in affected women, as well as assisting in comprehending the physiopathologic mechanisms underlying endometriosis. Mol. Reprod. Dev. 80: 441-450, 2013. (c) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:441 / 450
页数:10
相关论文
共 43 条
[1]
What's the delay? A qualitative study of women's experiences of reaching a diagnosis of endometriosis [J].
Ballard, Karen ;
Lowton, Karen ;
Wright, Jeremy .
FERTILITY AND STERILITY, 2006, 86 (05) :1296-1301
[2]
Visualizing networks [J].
Bell, George W. ;
Lewitrer, Fran .
DNA MICROARRAYS, PART B: DATABASES AND STATISTICS, 2006, 411 :408-+
[3]
Macrophage expression in endometrium of women with and without endometriosis [J].
Berbic, Marina ;
Schulke, Lauren ;
Markham, Robert ;
Tokushige, Natsuko ;
Russell, Peter ;
Fraser, Ian S. .
HUMAN REPRODUCTION, 2009, 24 (02) :325-332
[4]
Mechanisms of Disease Endometriosis [J].
Bulun, Serdar E. .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 360 (03) :268-279
[5]
CELL-ADHESION MOLECULES ON THE OOCYTE AND PREIMPLANTATION HUMAN EMBRYO [J].
CAMPBELL, S ;
SWANN, HR ;
SEIF, MW ;
KIMBER, SJ ;
APLIN, JD .
HUMAN REPRODUCTION, 1995, 10 (06) :1571-1578
[6]
D'Hooghe TM, 2003, SEMIN REPROD MED, V21, P243
[7]
DOODY MC, 1988, FERTIL STERIL, V49, P47
[8]
Follicular fluid in mammals [J].
Fahiminiya, S. ;
Gerard, N. .
GYNECOLOGIE OBSTETRIQUE & FERTILITE, 2010, 38 (06) :402-404
[9]
The effect of endometriosis, cycle stage, lymphocyte suppression and pregnancy on CA-125 levels in peritoneal fluid and serum in baboons [J].
Falconer, H ;
Bambra, CS ;
Chai, D ;
Cornillie, FJ ;
Hill, JA ;
D'Hooghe, TM .
HUMAN REPRODUCTION, 2005, 20 (11) :3033-3038
[10]
Garrido N, 2003, SEMIN REPROD MED, V21, P183