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Prognostic roles of Notch receptor mRNA expression in human ovarian cancer.
- Source :
-
Oncotarget [Oncotarget] 2017 May 16; Vol. 8 (20), pp. 32731-32740. - Publication Year :
- 2017
-
Abstract
- Aberrant activation of Notch signaling pathway has been correlated with high grade ovarian carcinoma and carcinogenesis. However, the predictive and prognostic values of Notch signaling pathway in ovarian cancer patients remains unclear. We utilize "The Kaplan-Meier plotter" (KM plotter) background database to access the prognostic values including overall survival (OS), progression-free survival (PFS), as well as post-progression survival (PPS) of four Notch receptor mRNA expression in ovarian cancer patients. Notch1 mRNA high expression was not correlated with OS, PFS and PPS for all ovarian cancer patients, but significantly correlated with poor PFS in TP53 wild type and favorite PFS in TP53 mutation type ovarian cancer patients. Notch2 mRNA high expression was significantly correlated with poor PFS for all ovarian cancer patients, especially in grade II patients. Notch3 mRNA high expression was significantly correlated with favorite PFS for all ovarian cancer patients. Notch4 mRNA high expression was significantly correlated with favorite OS, but not PFS and PPS for all ovarian cancer patients. The results strongly support that there are distinct prognostic values of four Notch receptor mRNA expression in ovarian cancer patients.
- Subjects :
- Biomarkers, Tumor genetics
Disease-Free Survival
Female
Gene Expression Profiling methods
Gene Expression Regulation, Neoplastic
Humans
Kaplan-Meier Estimate
Mutation
Neoplasm Grading
Prognosis
Receptor, Notch1 genetics
Receptor, Notch2 genetics
Receptor, Notch3 genetics
Receptor, Notch4 genetics
Signal Transduction
Ovarian Neoplasms genetics
Ovarian Neoplasms pathology
Receptors, Notch genetics
Tumor Suppressor Protein p53 genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1949-2553
- Volume :
- 8
- Issue :
- 20
- Database :
- MEDLINE
- Journal :
- Oncotarget
- Publication Type :
- Academic Journal
- Accession number :
- 28415574
- Full Text :
- https://doi.org/10.18632/oncotarget.16387