Sex steroid receptors in human myometrium and fibroids:: Changes during the menstrual cycle and gonadotropin-releasing hormone treatment

被引:147
作者
Englund, K
Blanck, A
Gustavsson, I
Lundkvist, U
Sjöblom, P
Norgren, A
Lindblom, B
机构
[1] Huddinge Univ Hosp, Karolinska Inst, Dept Clin Sci, Sect Obstet & Gynecol, SE-14186 Huddinge, Sweden
[2] Uppsala Univ, Sect Obstet & Gynecol, Dept Womens & Childrens Hlth, SE-75185 Uppsala, Sweden
关键词
D O I
10.1210/jc.83.11.4092
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The content of estrogen and progesterone receptors (ER, PR) is higher in fibroid tissue than in homologous myometrium, and both receptors seem to be regulated by the levels of circulating sex steroids. Myometrial and fibroid tissues were recovered-from women undergoing gynecological operations during different phases of the menstrual cycle and during treatment with an analogue of GnRH (GnRHa). Contents of ER and PR in the tissue cytosol were determined by enzyme immunoassay. The EB levels were significantly higher in fibroid tissue than in homologous myometrium in all the endocrine conditions. During the secretory phase, when luteal progesterone production is prominent, the ER levels in the myometrium and fibroids were lower than during the proliferative phase. During GnRHa treatment, the ER levels in both tissues were similar to those in the proliferative phase but significantly higher than in the secretory phase. The PR levels were also significantly higher in fibroids than in myometrium in all the different endocrine conditions. In both tissues, the PR levels were lower in the secretory phase and during GnRHa treatment, compared with the proliferative phase. Our data suggest that, in these categories of women, both ER and PR are overexpressed in fibroid tissue. Apparently, high progesterone levels down-regulate the ER in both fibroids and myometrium, whereas estrogen mediates the up-regulation of the PR during the proliferative phase. Increased knowledge about the mechanisms by which sex steroids regulate their own receptors in uterine tissues might provide a basis for development of new treatment strategies for women with fibroid disease.
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页码:4092 / 4096
页数:5
相关论文
共 20 条
  • [1] ADAMSON GD, 1992, AM J OBSTET GYNECOL, V166, P746
  • [2] ALVAREZMURPHY A, 1993, J CLIN ENDOCR METAB, V76, P513
  • [3] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [4] ESTROGEN-RECEPTOR GENE-EXPRESSION IN HUMAN UTERINE LEIOMYOMATA
    BRANDON, DD
    ERICKSON, TE
    KEENAN, EJ
    STRAWN, EY
    NOVY, MJ
    BURRY, KA
    WARNER, C
    CLINTON, GM
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (06) : 1876 - 1881
  • [5] PROGESTERONE-RECEPTOR MESSENGER-RIBONUCLEIC-ACID AND PROTEIN ARE OVEREXPRESSED IN HUMAN UTERINE LEIOMYOMAS
    BRANDON, DD
    BETHEA, CL
    STRAWN, EY
    NOVY, MJ
    BURRY, KA
    HARRINGTON, MS
    ERICKSON, TE
    WARNER, C
    KEENAN, EJ
    CLINTON, GM
    [J]. AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1993, 169 (01) : 78 - 85
  • [6] FIBROID GROWTH IN RESPONSE TO HIGH-DOSE PROGESTOGEN
    HARRISONWOOLRYCH, M
    ROBINSON, R
    [J]. FERTILITY AND STERILITY, 1995, 64 (01) : 191 - 192
  • [7] IMMUNOHISTOCHEMICAL ANALYSIS OF ESTROGEN-RECEPTORS, PROGESTERONE RECEPTORS AND KI-67 IN LEIOMYOMA AND MYOMETRIUM DURING THE MENSTRUAL-CYCLE AND PREGNANCY
    KAWAGUCHI, K
    FUJII, S
    KONISHI, I
    IWAI, T
    NABU, Y
    NONOGAKI, H
    ISHIKAWA, Y
    MORI, T
    [J]. VIRCHOWS ARCHIV A-PATHOLOGICAL ANATOMY AND HISTOPATHOLOGY, 1991, 419 (04) : 309 - 315
  • [8] PATHOPHYSIOLOGY OF UTERINE LEIOMYOMAS
    KOUTSILIERIS, M
    [J]. BIOCHEMISTRY AND CELL BIOLOGY, 1992, 70 (05) : 273 - 278
  • [9] IMMUNOFLUORESCENT ANALYSIS OF ESTROGEN INDUCTION OF PROGESTERONE-RECEPTOR IN THE RHESUS UTERUS
    OKULICZ, WC
    SAVASTA, AM
    HOBERG, LM
    LONGCOPE, C
    [J]. ENDOCRINOLOGY, 1989, 125 (02) : 930 - 934
  • [10] DIFFERENTIAL REDUCTION IN THE VOLUME OF LEIOMYOMA AND UTERUS DURING BUSERELIN TREATMENT
    PUZIGACA, Z
    PRELEVIC, GM
    SRETENOVIC, Z
    [J]. GYNECOLOGICAL ENDOCRINOLOGY, 1994, 8 (01) : 39 - 43