Current and future medical treatment for endometriosis
article
OA: diamond
CC0
AI-generated summary
Researchers investigated potential novel endometriosis treatments, finding that parthenolide and selective estrogen receptor modulators suppressed inflammation and proliferation, while Kampo medicine raised pain thresholds and inhibited IL-33.
One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works
Abstract
Although it is difficult to determine the actual incidence of endometriosis, an increase in the frequency of menstrual periods due to women's entry into the workforce and the trend toward late childbearing and low fertility are thought to be the reasons for the rising incidence. The characteristics of endometriosis include the need to preserve fertility in the majority of cases, and the association of dysmenorrhea in young patients with future development of endometriosis. We presented that IAP (Inhibitor of apoptotic protein) inhibitors have the potential to be novel agents for the treatment of endometriosis. A medicinal herb parthenolide and selective estrogen receptor modulator, which are found in a number of plants, suppressed inflammation and proliferation in human endometriosis cells and shrink mouse foci through NF-kB inhibition. We found that Kampo medicine raised the pain threshold in mice and inhibited IL-33 expression in endometriotic lesions. Recently, we have applied bioluminescence technology and knockout mouse models to non-invasively observe early lesions. I will explain the possibility of new therapeutic agents for endometriosis.
My notes (saved in your browser only)
Condition tags
Citation neighborhood (no data yet)
We don't have any in-corpus citations linked to this paper yet. The paper's references may be in our DB but unresolved to ``paper_id`` (resolution happens at ingest when the cited DOI matches a row we already have). Run the cross-source citation reconcile pass to retry.
Source provenance
- openalex
- last seen: 2026-06-10T17:14:06.276822+00:00
License: CC0
· commercial use OK