Suppr超能文献

预防乳腺癌的未来可能性:促黄体生成素释放激素激动剂

Future possibilities in the prevention of breast cancer: luteinizing hormone-releasing hormone agonists.

作者信息

Spicer D V, Pike M C

机构信息

USC/Norris Comprehensive Cancer Center and University of Southern California/Keck School of Medicine, Los Angeles, California 90089, USA.

出版信息

Breast Cancer Res. 2000;2(4):264-7. doi: 10.1186/bcr67. Epub 2000 May 24.

Abstract

The cyclic production of estrogen and progesterone by the premenopausal ovary accounts for the steep rise in breast cancer risk in premenopausal women. These hormones are breast cell mitogens. By reducing exposure to these ovarian hormones, agonists of luteinizing hormone-releasing hormone (LHRH) given to suppress ovarian function may prove useful in cancer prevention. To prevent deleterious effects of hypoestrogenemia, the addition of low-dose hormone replacement to the LHRH agonist appears necessary. Pilot data with such an approach indicates it is feasible and reduces mammographic densities.

摘要

绝经前卵巢周期性分泌雌激素和孕激素,这是绝经前女性患乳腺癌风险急剧上升的原因。这些激素是乳腺细胞有丝分裂原。通过减少对这些卵巢激素的接触,给予促黄体生成素释放激素(LHRH)激动剂以抑制卵巢功能,可能对癌症预防有用。为防止低雌激素血症的有害影响,在LHRH激动剂中添加低剂量激素替代似乎是必要的。采用这种方法的初步数据表明它是可行的,并能降低乳腺X线摄影密度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11b0/138786/6356dcc0e05c/bcr67-1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验