Jab1 expression is associated with inverse expression of p27(kip1) and poor prognosis in epithelial ovarian tumors
- PMID: 11751512
Jab1 expression is associated with inverse expression of p27(kip1) and poor prognosis in epithelial ovarian tumors
Abstract
Purpose: Jab1 (Jun activation domain-binding protein 1) has been described as a coactivtor of AP1 transcription factor, and is a subunit of a large protein complex (called the COP9 signalosome). Recent study (K. Tomoda et al., Nature (Lond.), 398: 160-165, 1999) found that Jab1 protein can cause breakdown of p27(kip1) protein in mammalian cells. To investigate whether Jab1 expression is correlated with p27(kip1) protein levels as well as how it might be clinically relevant, we evaluated the expression of Jab1 in a group of epithelial ovarian tumors.
Experimental design: Immunohistochemical analysis was performed in 80 cases of ovarian tumors (33 benign ovarian tumors and 47 ovarian carcinomas). Twenty-six of the 80 cases were evaluated by Western blot analysis.
Results: Jab1 overexpression was detected in 68.1% (32 of 47) of malignant tumors and 33.3% (11 of 33) of benign tumors. The positive ratio of Jab1 was increased from benign to malignant ovarian tumors (P = 0.002). A negative correlation between Jab1 and p27(kip1) expression was found in both benign (P = 0.003) and malignant (P = 0.002) ovarian tumors. No significant correlation was observed between Jab1 overexpression and clinicopathological parameters. Kaplan-Meier survival analysis showed that Jab1 overexpression was significantly associated with poor prognosis of patients (P = 0.049).
Conclusions: Jab1 expression is inversely correlated with p27(kip1) expression levels, and Jab1, as a negative regulator of p27(kip1), may be associated with the progression and prognosis of epithelial ovarian tumors.
Similar articles
-
The Relevance of Women's Diseases, Jun Activation-domain Binding Protein 1 (JAB1) and p27(kip1).J Menopausal Med. 2016 Apr;22(1):6-8. doi: 10.6118/jmm.2016.22.1.6. Epub 2016 Apr 26. J Menopausal Med. 2016. PMID: 27152307 Free PMC article. Review.
-
Jun activation domain binding protein 1 expression is associated with low p27(Kip1)levels in node-negative breast cancer.Clin Cancer Res. 2003 Nov 15;9(15):5652-9. Clin Cancer Res. 2003. PMID: 14654548
-
Clinical significance of Skp2 expression, alone and combined with Jab1 and p27 in epithelial ovarian tumors.Oncol Rep. 2006 Apr;15(4):765-71. Oncol Rep. 2006. PMID: 16525656
-
Jun activation domain-binding protein 1 expression in breast cancer inversely correlates with the cell cycle inhibitor p27(Kip1).Cancer Res. 2003 Jun 1;63(11):2977-81. Cancer Res. 2003. PMID: 12782606
-
JAB1/CSN5 and the COP9 signalosome. A complex situation.EMBO Rep. 2001 Feb;2(2):96-101. doi: 10.1093/embo-reports/kve028. EMBO Rep. 2001. PMID: 11258719 Free PMC article. Review.
Cited by
-
Targeting Jab1/CSN5 in nasopharyngeal carcinoma.Cancer Lett. 2012 Dec 30;326(2):155-60. doi: 10.1016/j.canlet.2012.07.033. Epub 2012 Aug 4. Cancer Lett. 2012. PMID: 22867945 Free PMC article. Review.
-
Genome-wide local ancestry approach identifies genes and variants associated with chemotherapeutic susceptibility in African Americans.PLoS One. 2011;6(7):e21920. doi: 10.1371/journal.pone.0021920. Epub 2011 Jul 6. PLoS One. 2011. PMID: 21755009 Free PMC article.
-
Emerging roles of Jab1/CSN5 in DNA damage response, DNA repair, and cancer.Cancer Biol Ther. 2014 Mar 1;15(3):256-62. doi: 10.4161/cbt.27823. Epub 2014 Feb 4. Cancer Biol Ther. 2014. PMID: 24495954 Free PMC article. Review.
-
The Relevance of Women's Diseases, Jun Activation-domain Binding Protein 1 (JAB1) and p27(kip1).J Menopausal Med. 2016 Apr;22(1):6-8. doi: 10.6118/jmm.2016.22.1.6. Epub 2016 Apr 26. J Menopausal Med. 2016. PMID: 27152307 Free PMC article. Review.
-
Pan-cancer analyses of Jab1/COPS5 reveal oncogenic role and clinical outcome in human cancer.Heliyon. 2022 Dec 23;8(12):e12553. doi: 10.1016/j.heliyon.2022.e12553. eCollection 2022 Dec. Heliyon. 2022. PMID: 36643321 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources
Medical
Research Materials
Miscellaneous