Sex hormone regulation of survivin gene expression

被引:26
作者
Nabilsi, Nancy H. [1 ]
Broaddus, Russell R. [2 ]
McCampbell, Adrienne S. [2 ]
Lu, Karen H. [3 ]
Lynch, Henry T. [4 ]
Chen, Lee-may [5 ]
Loose, David S. [1 ]
机构
[1] Univ Texas Hlth Sci Ctr Houston, Dept Integrat Biol & Pharmacol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Gynecol Oncol, Houston, TX 77030 USA
[4] Creighton Univ, Sch Med, Dept Prevent Med & Publ Hlth, Omaha, NE 68131 USA
[5] Univ Calif San Francisco, Dept Gynecol Oncol, San Francisco, CA 94143 USA
关键词
ENDOMETRIAL STROMAL CELLS; GROWTH-FACTOR-I; ESTROGEN; CARCINOMA; APOPTOSIS; CANCER; PROGESTIN; RECEPTOR; RELAXIN; IGFBP-1;
D O I
10.1677/JOE-10-0128
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Survivin (BIRC5) is a cell survival gene that is overexpressed in endometrial cancer and has been implicated to have a physiological role in normal endometrial function. To determine whether survivin gene expression is regulated by reproductive steroid hormones in the human endometrium, RNA was prepared from normal cycling women in the proliferative and secretory phases of the menstrual cycle. RNA was also isolated from 21 endometrial biopsies from premenopausal women at baseline and following 3 months of treatment with depot medroxyprogesterone acetate. Finally, RNA was isolated from endometrial biopsies from ten healthy postmenopausal women participating in a clinical trial of estrogen replacement therapy at baseline and following 6 months of treatment with conjugated equine estrogen. Quantitative RT-PCR analysis was used to determine survivin, insulin-like growth factor binding protein 1 (IGFBP1), Ki67, and IGF1 gene expression levels. Survivin gene expression was highest in the proliferative phase of the menstrual cycle and showed a statistically significant 4-fold increase in expression following chronic treatment with estrogens; this was strongly correlated with increased Ki67, a marker of proliferation. Survivin gene expression decreased 4.6-fold following chronic progestin treatment in the human endometrium. These data suggest that survivin transcript is regulated by estrogens and progestins in the disease-free human endometrium. The data also suggest that survivin transcript may be used as a biomarker of estrogen and progestin treatment efficacy, but validation studies must be conducted to support this conclusion. Journal of Endocrinology (2010) 207, 237-243
引用
收藏
页码:237 / 243
页数:7
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