Combination of 4-HPR and oral contraceptive in monkey model of chemoprevention of ovarian cancer

被引:6
作者
Brewer, Molly
Ranger-Moore, James
Satterfield, William
Hao, Zengping
Wang, Jian
Brewer, Emily
Wharton, J. Taylor
Bast, Robert
Zou, Changping
机构
[1] Univ Arizona, Coll Med, Dept Ob Gyn, Tucson, AZ 85724 USA
[2] Univ Arizona, Coll Publ Hlth, Tucson, AZ 85724 USA
[3] MD Anderson Canc Ctr, Dept Vet Sci, Houston, TX 77030 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2007年 / 12卷
关键词
4-HPR; OCP; ovarian cancer; monkey;
D O I
10.2741/2228
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
4-(N-hydroxyphenyl) retinamide (4-HPR) and the oral contraceptives (OCP) are currently being used alone, and in combination, for the prevention of ovarian cancer. However, the mechanism of their effects has not been studied. Non-human primate models are ideal for studying the role of these and other drugs for cancer chemoprevention because of the genetic similarity between primates and humans in respect to hormone regulation and menstrual cycle. 4-HPR and OCP were administered to sixteen female adult Macacca mulatta (Rhesus macaques) for three months alone and in combination. Laparotomy was performed before and after treatment, and ovarian biopsies were obtained to evaluate the expression of retinoid and hormone receptors, and apoptosis. ER alpha was undetectable, but ER beta, PR, RXR alpha, and RXR gamma were constitutively expressed in the ovaries. 4-HPR induced RXRa and RXR gamma expression at a low level and, OCP induced expression of ER beta. However, the combination of 4-HPR with OCP had a larger effect on expression of retinoid receptors. Apoptosis was detected in the 4-HPR group (equivalent dose: 200 mg/day). The results provide a rationale for the use of the Rhesus macaque as a model for ovarian cancer chemoprevention.
引用
收藏
页码:2260 / 2268
页数:9
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