Notch1 ligand signaling pathway activated in cervical cancer: poor prognosis with high-level JAG1/Notch1

Objective Notch signalings are regulated multiple cellular processes during cancer progression. We aimed to investigate the significance and prognostic value of expression of Notch1 and JAG1 in cervical cancer to determine whether they could serve as prognostic predictors. Methods/materials The expr...

Full description

Saved in:
Bibliographic Details
Published inArchives of gynecology and obstetrics Vol. 292; no. 4; pp. 899 - 904
Main Authors Yousif, Nasser Ghaly, Sadiq, Alaa Muhammad, Yousif, Maitham G., Al-Mudhafar, Rihab H., Al-Baghdadi, Jinan J., Hadi, Najah
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Springer Berlin Heidelberg 01.10.2015
Springer Nature B.V
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Objective Notch signalings are regulated multiple cellular processes during cancer progression. We aimed to investigate the significance and prognostic value of expression of Notch1 and JAG1 in cervical cancer to determine whether they could serve as prognostic predictors. Methods/materials The expression of Notch1/JAGD1 was investigated by real-time PCR, western blot assay and its association with overall survival of patients was analyzed by statistical analysis. Results Notch1 and JAGD1 expression level were significantly elevated in cervical cancer in comparison to normal specimens and other types of Notch receptors and ligands. It is also proved that Notch1 and JAGD1 expression were to be associated with cervical cancer invasion, lymph node metastasis, and FIGO system. In addition, survival analysis proved that elevated Notch1 and JAGD1 expression were associated with poor overall survival of patients ( P  = 0.01, P  = 0.02 log-rank test), respectively. Conclusions The present data proved the over-expression of Notch1/JAGD1 and its association with tumor progression in human cervical cancer, which might be a potential valuable biomarker for cervical cancer and further studies need.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0932-0067
1432-0711
DOI:10.1007/s00404-015-3694-1