The Relevance of Women's Diseases, Jun Activation-domain Binding Protein 1 (JAB1) and p27(kip1).

OA: gold
AI-generated deep summary by qwen3.7-flash, 2026-08-24 · read from full text

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

The Jun activation-domain binding protein 1 (Jab1) recognize a potential coactivator of activator protein 1 (AP-1) such as c-fos, c-jun transcription factor and the fifth subunit of the COP9 signalosome complex. Also, Jab1 activate the c-jun gene resulted cell proliferation. Not only a powerful tumor suppressor but also regulator of apoptosis negative cdk inhibitor p27(kip1) are involved in the cell cycle. This is Jab1 and p27(kip1) interact with each other, Jab1 accelerate p27(kip1) from nuclear to cytoplasm through ubiquitin/proteasome pathway. However, information about the relationship between Jab1 and p27(kip1) is not known much. Taken together, the results of this study identify function and structure of Jab1 and p27(kip1) were described in a recent article on the basis of relevant. Besides Jab1 and p27(kip1) will organize the relationship between the disease and women.
Full text 6,652 characters · extracted from pmc-nxml · 4 sections · click to expand

P27

Endometriosis is the endometrial tissue in the uterus that should be present in the abdominal cavity outside the uterus, 9 a common disease that occurs in approximately 10 to 15% woman of childbearing age. The cause of endometriosis, though not known as yet, regurgitation of menstrual blood, immunological factors, genetic factors and family history factors have been established occurrence of endometriosis. According to previous research compared to the healthy women were reported for endometriosis and endometriosis in infertile women, following studies have been reported to demonstrate the changes in the endometrium of women with disease. 10 11 Moreover the before-mentioned transformation demanded the establishment of the endometrium in the peritoneal, recent evidence indicated that uterine mucosal cells of patients with endometriosis do not follow the normal growth pattern and apoptosis. 12 13 14 In the midst of CDK inhibitors, we should be focused on p27 kip1 . The critical function of p27 kip1 is to inhibit CDK-cyclin E complex by controlling a checkpoint in the G1 in normal cells. When p27 kip1 is not present in the cells, cells are not follow a cell cycle control signal and proliferation. 15 Because endometrial cell cycle changes may be involved in cell cycle regulation of endometriosis in women with diseases significance of p27 kip1 protein level it can be seen that a change in the lining of a particular cell cycle is important.

Jab1

Ovarian cancer is malignant tumor, the most widely occurring between 50 to 70 years old woman. 16 17 The second most common cause of gynecologic cancer in succession cervical cancer has been identified as a family history, a lot of ovulation number. No proven method for ovarian cancer is often rapidly progressive and fatal disease early symptoms rarely. 5 As a negative regulator of the cell cycle, p27 kip1 is tumor suppressor, 6 which inhibits cyclin-CDK in a dosage dependent manner to control cell cycle progression. 7 8 Recently, decreased expression of p27 kip1 has been frequently detected in human cancers, 5 10 11 12 13 14 15 including ovarian carcinoma. Recently, the expression of Jab1 and p27 kip1 in a malignant epithelial ovarian cancer, was found to be correlated with the reverse p27 kip1 expression levels as a result Jab1 negative regulator. 18 That is a negative regulator of p27 kip1 Jab1 has been associated with the development of the ovarian tumor, progression and prognosis.

Intro

The Jun activation-domain binding protein 1 (Jab1) is initially identified as a coactivator of activator protein (AP-1) transcription factor and found a component of the COP9 signalosome (CSN) complex, contained modulating signal transduction, gene transcription, and protein stability. 1 2 Jab1 interacted with p27 kip1 and translocate it's from nuclear to cytoplasm which resulted in acceleration of p27 kip1 degradation through the ubiquitin-dependent/proteasome pathway and promotes cell-cycle progression. 3 p27 kip1 is an inhibitor of cyclin-dependent kinases (CDKs), performing potential tumor suppressor gene in diversity of human's cancer. CDK is a family of protein kinases, the activity of the serine/threonine kinases known as cdk that are under the strict control of positive and negative regulators. Until now studies have found that p27 kip1 promotes apoptosis, growth inhibition and cell cycle arrest. 4 5 Reduction of p27 kip1 protein means high resistance and poor prognosis to anticancer drug. Down regulation of p27 kip1 protein is often discovered by human cancers including breast and ovarian cancer and is normally correlated with poor clinical outcome. As a result, the concentration of the p27 kip1 protein can be expressed as an important marker in the development of human cancer. Accordingly, this study examines a correlation of p27 kip1 and Jab1, will reveal the relevant disease in women.

Summary

Jab1 is a protein that enhances the activity of the c-jun gene and induce cell proliferation, p27 kip1 is a strong reduction in the tumor suppressor gene p27 kip1 has a high resistance and poor prognosis in cancer. Also p27 kip1 has an important role cell cycle regulatory factors. Recently, Jab1 and p27 kip1 has been reported that many women involved in diseases such as breast cancer, endometriosis and ovarian cancer. As well as Jab1 and p27 kip1 started to reveal that the association became known widely in hepatocellular carcinoma, laryngeal carcinoma and nerves. In conclusion, a wide range of research on Jab1 and p27 kip1 is expected to play a major role in reproductive system, kidney, blood vessel tissues and nerves system further physiological pathophysiological.

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)

Ask this paper AI returns verbatim quotes from the full text · source: pmc-nxml

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: 2026-08-30T09:23:35.175841+00:00