Endometriosis and the neoplastic process

被引:170
作者
Varma, R [1 ]
Rollason, T
Gupta, JK
Maher, ER
机构
[1] Birmingham Womens Hosp, Sch Med & Mol Genet, Birmingham B15 2TG, W Midlands, England
[2] Birmingham Womens Hosp, Dept Histopathol, Birmingham B15 2TG, W Midlands, England
[3] Birmingham Womens Hosp, Acad Dept Obstet & Gynaecol, Birmingham B15 2TG, W Midlands, England
关键词
D O I
10.1530/rep.1.00020
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Endometriosis is a frequent disorder that commonly presents with infertility and pelvic pain. Although the precise aetiology of endometriosis is unclear, it is generally considered to involve multiple genetic, environmental, immunological, angiogenic and endocrine processes. Genetic factors have been implicated in endometriosis but the susceptibility genes remain largely unknown. Although endometriosis is a benign disorder, recent studies of endometriosis suggest endometriosis could be viewed as a neoplastic process. Evidence to support this hypothesis includes the increased susceptibility to develop ovarian clear-cell and endometrioid cancers in the presence of endometriosis, and molecular similarities between endometriosis and cancer. In this article we discuss (i) the evidence suggesting that endometriosis might be viewed as a neoplastic process, and (ii) the implications of this hypothesis for elucidating the pathogenesis of endometriosis and developing novel methods of diagnostic classification and individualised treatments.
引用
收藏
页码:293 / 304
页数:12
相关论文
共 111 条
[1]   Left lateral predisposition of endometriosis and endometrioma [J].
Al-Fozan, H ;
Tulandi, T .
OBSTETRICS AND GYNECOLOGY, 2003, 101 (01) :164-166
[2]   CYP1A1, CYP19, and GSTM1 polymorphisms increase the risk of endometriosis [J].
Arvanitis, DA ;
Koumantakis, GE ;
Goumenou, AG ;
Matalliotakis, IM ;
Koumantakis, EE ;
Spandidos, DA .
FERTILITY AND STERILITY, 2003, 79 :702-709
[3]   Progesterone receptor isoform A but not B is expressed in endometriosis [J].
Attia, GR ;
Zeitoun, K ;
Edwards, D ;
Johns, A ;
Carr, BR ;
Bulun, SE .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (08) :2897-2902
[4]   OVARIAN ENDOMETRIOTIC CYSTS - AN ANALYSIS OF CYTOLOGIC ATYPIA AND DNA-PLOIDY PATTERNS [J].
BALLOUK, F ;
ROSS, JS ;
WOLF, BC .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1994, 102 (04) :415-419
[5]   The genetics and genomics of cancer [J].
Balmain, A ;
Gray, J ;
Ponder, B .
NATURE GENETICS, 2003, 33 (Suppl 3) :238-244
[6]   Possible involvement of arylamine N-acetyltransferase 2, glutathione S-transferases M1 and T1 genes in the development of endometriosis [J].
Baranova, H ;
Canis, M ;
Ivaschenko, T ;
Albuisson, E ;
Bothorishvilli, R ;
Baranov, V ;
Malet, P ;
Bruhat, MA .
MOLECULAR HUMAN REPRODUCTION, 1999, 5 (07) :636-641
[7]   GSTM1 null polymorphism and susceptibility to endometriosis and ovarian cancer [J].
Baxter, SW ;
Thomas, EJ ;
Campbell, IG .
CARCINOGENESIS, 2001, 22 (01) :63-65
[8]  
Bayani J, 2002, CANCER RES, V62, P3466
[9]  
Bayramoglu Hatice, 2001, Pathology and Oncology Research, V7, P33
[10]   Dioxins and endometriosis: A plausible hypothesis [J].
Birnbaum, LS ;
Cummings, AM .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2002, 110 (01) :15-21