Mechanisms of excessive estrogen formation in endometriosis

被引:82
作者
Bulun, SE
Gurates, B
Fang, ZJ
Tamura, M
Sebastian, S
Zhou, HF
Amin, S
Yang, SJ
机构
[1] Univ Illinois, Dept Obstet & Gynecol, Chicago, IL 60612 USA
[2] Univ Illinois, Dept Mol Genet, Chicago, IL 60612 USA
关键词
aromatase; aromatase inhibitor; endometriosis; estrogen; estrogen biosynthesis; metabolism; 17 beta-hydroxysteroid dehydrogenase type 2; steroidogenesis; osteoporosis; progesterone; cyclo-oxygenase; prostaglandin E-2;
D O I
10.1016/S0165-0378(01)00132-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Estrogen is produced in a number of human tissues including the ovary, placenta and extraglandular sites such as adipose tissue, skin and the brain. Aromatase is the key enzyme that regulates estrogen formation in these tissues. Aromatase activity is not detectable in normal endometrium. In contrast, aromatase is expressed aberrantly in endometriosis and is stimulated by PGE(2). This results in local production of estrogen, which induces PGE(2) formation and establishes a positive feedback cycle. Another abnormality in endometriosis, i.e. deficient 17beta-hydroxysteroid dehydrogenase (17beta-HSD) type 2 expression, impairs the inactivation of estradiol to estrone. These molecular aberrations collectively favor accumulation of increasing quantities of estradiol and PGE2 in endometriosis. The clinical relevance of these findings was exemplified by the successful treatment of an unusually aggressive case of postmenopausal endometriosis using an aromatase inhibitor. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:21 / 33
页数:13
相关论文
共 31 条
[1]   AROMATIZATION OF ANDROSTENEDIONE BY HUMAN ADIPOSE-TISSUE STROMAL CELLS IN MONOLAYER-CULTURE [J].
ACKERMAN, GE ;
SMITH, ME ;
MENDELSON, CR ;
MACDONALD, PC ;
SIMPSON, ER .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1981, 53 (02) :412-417
[2]   Physiology and molecular genetics of 17 beta-hydroxysteroid dehydrogenases [J].
Andersson, S ;
Moghrabi, N .
STEROIDS, 1997, 62 (01) :143-147
[3]   Suppression of matrix metalloproteinases inhibits establishment of ectopic lesions by human endometrium in nude mice [J].
Bruner, KL ;
Matrisian, LM ;
Rodgers, WH ;
Gorstein, F ;
Osteen, KG .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (12) :2851-2857
[4]   EXPRESSION OF THE CYP19 GENE AND ITS PRODUCT AROMATASE CYTOCHROME-P450 IN HUMAN UTERINE LEIOMYOMA TISSUES AND CELLS IN CULTURE [J].
BULUN, SE ;
SIMPSON, ER ;
WORD, RA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 78 (03) :736-743
[5]   A LINK BETWEEN BREAST-CANCER AND LOCAL ESTROGEN BIOSYNTHESIS SUGGESTED BY QUANTIFICATION OF BREAST ADIPOSE-TISSUE AROMATASE CYTOCHROME-P450 TRANSCRIPTS USING COMPETITIVE POLYMERASE CHAIN-REACTION AFTER REVERSE TRANSCRIPTION [J].
BULUN, SE ;
PRICE, TM ;
AITKEN, J ;
MAHENDROO, MS ;
SIMPSON, ER .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1993, 77 (06) :1622-1628
[6]   POLYMERASE CHAIN-REACTION AMPLIFICATION FAILS TO DETECT AROMATASE CYTOCHROME-P450 TRANSCRIPTS IN NORMAL HUMAN ENDOMETRIUM OR DECIDUA [J].
BULUN, SE ;
MAHENDROO, MS ;
SIMPSON, ER .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1993, 76 (06) :1458-1463
[7]   PERITONEAL-MACROPHAGES FROM PATIENTS WITH ENDOMETRIOSIS RELEASE GROWTH-FACTOR ACTIVITY INVITRO [J].
HALME, J ;
WHITE, C ;
KAUMA, S ;
ESTES, J ;
HASKILL, S .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1988, 66 (05) :1044-1049
[8]   ADMINISTRATION OF NASAL NAFARELIN AS COMPARED WITH ORAL DANAZOL FOR ENDOMETRIOSIS - A MULTICENTER DOUBLE-BLIND COMPARATIVE CLINICAL-TRIAL [J].
HENZL, MR ;
CORSON, SL ;
MOGHISSI, K ;
BUTTRAM, VC ;
BERQVIST, C ;
JACOBSON, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 318 (08) :485-489
[9]  
HILL JA, 1992, FERTIL STERIL, V58, P262
[10]  
HUANG JC, 1996, P AM SOC REPR MED M