Sex steroidal regulation of uterine leiomyoma growth and apoptosis

被引:219
作者
Maruo, T [1 ]
Ohara, N [1 ]
Wang, J [1 ]
Matsuo, H [1 ]
机构
[1] Kobe Univ, Grad Sch Med, Dept Obstet & Gynecol, Chuo Ku, Kobe, Hyogo 6500017, Japan
关键词
apoptosis; GnRH agonist; growth factor; leiomyoma; sex steroid hormone;
D O I
10.1093/humupd/dmh019
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Uterine leiomyomas develop during the reproductive years and regress after menopause, indicating ovarian steroid-dependent growth potential. Although the clinical and biochemical observations have traditionally supported an important role for estrogen in the promotion of leiomyoma growth, there is also increasing evidence to suggest the involvement of progesterone in the pathogenesis of leiomyoma. In this review, much attention has been paid to characterizing the molecular mechanisms of sex steroidal regulation of leiomyoma growth and apoptosis by evaluating the effects of sex steroids on the expression of growth factors and apoptosis-related factors. The effects of GnRH agonist on the expression of these factors in leiomyoma are also described. 17beta-Estradiol up-regulates epidermal growth factor (EGF) receptor, but down-regulates p53 protein in leiomyoma cells, whereas progesterone augments EGF and Bcl-2 protein, but inhibits insulin-like growth factor (IGF-I) and tumour necrosis factor (TNFalpha). Since it is now evident that EGF and IGF-I act as local factors which stimulate leiomyoma growth, these findings suggest that progesterone may have dual actions, stimulatory and inhibitory, on leiomyoma cell growth and survival, depending on the local growth factor conditions around each leiomyoma. This may explain why the size of uterine leiomyomas during the use of levonorgestrel-releasing intrauterine system (LNG-IUS) increases in some but decreases in other instances. This may also explain why the size of leiomyomas during pregnancy does not increase despite the overwhelming increase in circulating concentrations of sex steroid hormones. Moreover, there is further evidence to suggest that the interactions between estrogen receptors and progesterone receptors may be involved in the modulation of gene transcription activity in leiomyoma. This review demonstrates that leiomyoma growth is integrally regulated by the complex cross-talk between sex steroid hormones and growth factors.
引用
收藏
页码:207 / 220
页数:14
相关论文
共 182 条
[51]   p53 tumor suppressor protein content in human uterine leiomyomas and its down-regulation by 17β-estradiol [J].
Gao, ZJ ;
Matsuo, H ;
Nakago, S ;
Kurachi, O ;
Maruo, T .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (08) :3915-3920
[52]   Quantification of vascular endothelial growth factor-A in leiomyomas and adjacent myometrium [J].
Gentry, CC ;
Okolo, SO ;
Fong, LFWT ;
Crow, JC ;
Maclean, AB ;
Perrett, CW .
CLINICAL SCIENCE, 2001, 101 (06) :691-695
[53]   UTERINE INSULIN-LIKE GROWTH FACTOR-I RECEPTORS - REGULATION BY ESTROGEN AND VARIATION THROUGHOUT THE ESTROUS-CYCLE [J].
GHAHARY, A ;
MURPHY, LJ .
ENDOCRINOLOGY, 1989, 125 (02) :597-604
[54]   INSULIN-LIKE GROWTH-FACTOR (IGF), IGF BINDING-PROTEIN (IGFBP), AND IGF RECEPTOR GENE-EXPRESSION AND IGFBP SYNTHESIS IN HUMAN UTERINE LEIOMYOMATA [J].
GIUDICE, LC ;
IRWIN, JC ;
DSUPIN, BA ;
PANNIER, EM ;
JIN, IH ;
VU, TH ;
HOFFMAN, AR .
HUMAN REPRODUCTION, 1993, 8 (11) :1796-1806
[55]  
GLOUDEMANS T, 1990, CANCER RES, V50, P6689
[56]   Preferential stimulation of human progesterone receptor B expression by estrogen in T-47D human breast cancer cells [J].
Graham, JD ;
Roman, SD ;
McGowan, E ;
Sutherland, RL ;
Clarke, CL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (51) :30693-30700
[57]   NUCLEOTIDE-SEQUENCE OF EPIDERMAL GROWTH-FACTOR CDNA PREDICTS A 128,000-MOLECULAR WEIGHT PROTEIN-PRECURSOR [J].
GRAY, A ;
DULL, TJ ;
ULLRICH, A .
NATURE, 1983, 303 (5919) :722-725
[58]  
Hague S, 2000, CLIN CANCER RES, V6, P2808
[59]   LOCALIZATION AND QUANTIFICATION OF VASCULAR ENDOTHELIAL GROWTH-FACTOR MESSENGER-RIBONUCLEIC-ACID IN HUMAN MYOMETRIUM AND LEIOMYOMATA [J].
HARRISONWOOLRYCH, ML ;
SHARKEY, AM ;
CHARNOCKJONES, DS ;
SMITH, SK .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (06) :1853-1858
[60]   QUANTIFICATION OF MESSENGER-RIBONUCLEIC-ACID FOR EPIDERMAL GROWTH-FACTOR IN HUMAN MYOMETRIUM AND LEIOMYOMATA USING REVERSE-TRANSCRIPTASE POLYMERASE CHAIN-REACTION [J].
HARRISONWOOLRYCH, ML ;
CHARNOCKJONES, DS ;
SMITH, SK .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 78 (05) :1179-1184