米非司酮
孕酮受体
受体
兴奋剂
癌症
癌症研究
内分泌学
内科学
医学
生物
药理学
怀孕
雌激素受体
遗传学
乳腺癌
作者
Jerome H. Check,Diane Check
标识
DOI:10.1080/17446651.2023.2166487
摘要
The marked clinical improvement following 200-300 mg of mifepristone is likely related to blocking PIBF. In the low dosage used, mifepristone likely acts as an agonist for PGRMC-1 protein. Mifepristone may be less effective for cancers positive for the nPR because the nPR may be protective and blocking it may have detrimental effects. Based on this hypothetical model, the development of other potential treatment options to provide even greater efficacy for treating cancer are discussed.
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