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Updated: May 15, 2026

Integration of Bioinformatics Approaches and Experimental Validations to Understand the Role of Notch Signaling in Ovarian Cancer
Published on: January 12, 2020
Down-regulated expression of Notch signaling molecules in human endometrial cancer
Violeta Jonusiene1, Ausra Sasnauskiene, Nadezda Lachej
1Department of Biochemistry and Biophysics, Faculty of Natural Sciences, Vilnius University, Vilnius, Lithuania. violeta.jonusiene@gf.vu.lt
Abstract:
Notch signaling pathway is a highly conserved developmental pathway, which plays an important role in the regulation of cellular proliferation, differentiation and apoptosis. Deregulation of Notch pathway has been connected with the carcinogenesis in a variety of cancers. In this study, we investigated the expression of Notch receptors (NOTCH1, NOTCH2, NOTCH3 and NOTCH4), ligands (JAG1, JAG2 and DLL1) and target gene HES1. Fifty paired samples of endometrial cancer and adjacent nontumor endometrial tissue from endometrial cancer patients were analyzed by quantitative PCR. The mRNA levels of all investigated molecules were lower in endometrial cancer compared to adjacent nontumor tissue. The expression of NOTCH1, NOTCH4 and DLL1 in IB stage adenocarcinoma was significantly lower (P < 0.05) than the expression in IA stage adenocarcinoma. Significant correlations were found between mRNA expression levels of Notch target gene HES1 and several Notch signaling molecules: NOTCH1, NOTCH3, DLL1 (P < 0.001) and NOTCH2, JAG2 (P < 0.05). This supports the notion that Notch pathway can function as tumor suppressor in human endometrial cancer.
Insights
The Notch signaling pathway, crucial for cell regulation, appears to act as a tumor suppressor in endometrial cancer. Its key molecules were found at lower levels in cancerous tissues, suggesting a protective role.
Area of Science:
- Oncology
- Molecular Biology
- Cell Signaling
Background:
- The Notch signaling pathway is vital for cellular processes like proliferation and differentiation.
- Aberrant Notch pathway activity is linked to various cancers, but its role in endometrial cancer is not fully understood.
Purpose of the Study:
- To investigate the expression levels of Notch receptors (NOTCH1-4), ligands (JAG1-2, DLL1), and the target gene HES1 in endometrial cancer.
- To determine the correlation between Notch pathway molecules and endometrial cancer progression and stage.
Main Methods:
- Quantitative PCR was used to analyze mRNA expression of Notch pathway components.
- Fifty paired samples of endometrial cancer and adjacent non-tumor tissues were analyzed.
Main Results:
- mRNA levels of all studied Notch molecules were significantly lower in endometrial cancer tissues compared to adjacent non-tumor tissues.
- Expression of NOTCH1, NOTCH4, and DLL1 was significantly lower in Stage IB adenocarcinoma than in Stage IA.
- HES1 expression showed significant correlations with NOTCH1, NOTCH3, DLL1, NOTCH2, and JAG2.
Conclusions:
- The findings suggest that the Notch signaling pathway may function as a tumor suppressor in human endometrial cancer.
- Downregulation of Notch pathway components is associated with endometrial cancer development and progression.
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