Suppression of testosterone stimulates recovery of spermatogenesis after cancer treatment

被引:21
作者
Meistrich, ML [1 ]
Shetty, G [1 ]
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Expt Radiat Oncol, Houston, TX 77030 USA
来源
INTERNATIONAL JOURNAL OF ANDROLOGY | 2003年 / 26卷 / 03期
关键词
gonadotropin releasing hormone analogues; procarbazine; radiation; spermatogonia; testosterone;
D O I
10.1046/j.1365-2605.2003.00400.x
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
It is important to develop methods to prevent or reverse the infertility caused by chemotherapy or radiation therapy for cancer in men. Radiation and some chemotherapeutic agents kill spermatogonial stem cells, but we have shown that these cells survive in rats, although they are unable to differentiate. There is evidence that this phenomenon also occurs in men. The block to spermatogonial differentiation in rats is caused by some unknown change, either in the spermatogonia or the somatic elements of the testis, such that testosterone inhibits spermatogonial differentiation. In the rat, the spermatogenesis and fertility lost following treatment with radiation or some chemotherapeutic agents can be restored by suppressing testosterone with gonadotropin releasing hormone (GnRH) agonists or antagonists, either before or after the cytotoxic insult. The applicability of this procedure to humans is still unknown. Some anticancer regimens may kill all the stem cells, in which case the only option would be spermatogonial transplantation. However, in some cases stem cells survive and there is one report of stimulation of recovery of spermatogenesis with hormonal treatment. Clinical trials should focus on treating patients with hormones during or soon after anticancer treatment. The hormone regimen should involve suppression of testosterone production with minimum androgen supplementation used to improve the diminished libido.
引用
收藏
页码:141 / 146
页数:6
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