Therapeutic-antagonists of oestrogens can be produced for cancer and other therapies using cytochromes P450 (CYP)
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- 作者：Alan Wiseman
- 关键词：Autism ; Autism spectrum disorders ; Spironolactone ; Androgen ; Testosterone ; Neuroglia ; Neuroinflammation ; Inflammation ; Immune dysregulation ; Anti-inflammatory ; Anti-androgen
- 刊名：Medical Hypotheses
- 出版年：2005
- 出版时间：2005
- 年：2005
- 卷：65
- 期：6
- 页码：1088-1090
- 全文大小：69 K
文摘
Oestrogens such as 17β-oestradiol initiates nuclear-gene transcription in gender-specified tissues such as the ovaries and mammaries; and unfortunately too in cancer cells derived from target tissues. Consequently, there has been the development of novel agents for particular cancer therapies that are antagonists of oestrogens for oestrogen-receptor (ER) binding and of drugs with ER-specific interference RNA (RNAi) abilities. Therapeutic-antagonists of oestrogens will be re-designed and biosynthesised and deployed to circumvent the gene DNA-transcription abilities of oestrogens and mimics: and their metabolites in oestrogen-target tissues (see above). Furthermore, opportunities will emerge for adjunct-chemotherapy of particular tissue cancers: and in the prevention of recurrence outcomes. Cytochromes P450 can play an important part in these developments especially for the production of novel metabolites of oestrogens as therapeutic-antagonists of oestrogen-stimulated cancers.