The Relevance of Women's Diseases, Jun Activation-domain Binding Protein 1 (JAB1) and p27(kip1)
This review describes the structure and function of Jab1 and p27(kip1), detailing their interaction via the ubiquitin/proteasome pathway to propose a relationship between these proteins and women's diseases.
One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works
This review examines the molecular interplay between Jun activation-domain binding protein 1 (JAB1) and the cyclin-dependent kinase inhibitor p27(kip1), focusing on their roles in cell cycle regulation and cancer progression. The authors detail how JAB1 facilitates the cytoplasmic translocation and subsequent degradation of p27(kip1), a mechanism that promotes uncontrolled cell proliferation and is implicated in various malignancies such as breast and ovarian cancers. While the primary discussion centers on oncogenic processes, the text explicitly connects these pathways to endometriosis by suggesting that altered cell cycle control and apoptosis resistance in endometrial cells may drive the disease's pathophysiology. Relevance to endometriosis: listed as one indication for GnRH antagonists, though the paper's main focus is uterine fibroids.
Read from the paper's body, not the abstract. Not a substitute for reading the paper. No clinical advice. How this works
Abstract
Full text
6,652 characters
· extracted from
pmc-nxml
· 4 sections
· click to expand
P27
Jab1
Intro
Summary
Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.
My notes (saved in your browser only)
Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works
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
- europepmc
- last seen: 2026-10-18T09:30:06.152893+00:00
- pubmed
- last seen: 2026-10-08T21:17:51.490942+00:00