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Published on: January 12, 2020
Notch1 is a 5-fluorouracil resistant and poor survival marker in human esophagus squamous cell carcinomas
Jian Liu1, Huijie Fan, Yuanyuan Ma
1Department of Pathology, The First Teaching Hospital of Zhengzhou University, Basic Medical College, Zhengzhou University, Zhengzhou, Henan Province, China.
Abstract:
Notch signaling involves the processes that govern cell proliferation, cell fate decision, cell differentiation and stem cell maintenance. Due to its fundamental role in stem cells, it has been speculated during the recent years that Notch family may have critical functions in cancer stem cells or cancer cells with a stem cell phenotype, therefore playing an important role in the process of oncogenesis. In this study, expression of Notch family in KYSE70, KYSE140 and KYSE450 squamous esophageal cancer cell lines and virus transformed squamous esophageal epithelial cell line Het-1A was examined by quantitative RT-PCR. Compared to the Het-1A cells, higher levels of Nocth1 and Notch3 expression in the cancer cell lines were identified. Due to the finding that NOTCH3 mainly mediates squamous cell differentiation, NOTCH1 expression was further studied in these cell lines. By Western blot analyses, the KYSE70 cell line which derived from a poorly differentiated tumor highly expressed Notch1, and the Notch1 expression in this cell line was hypoxia inducible, while the KYSE450 cell line which derived from a well differentiated tumor was always negative for Notch1, even in hypoxia. Additional studies demonstrated that the KYSE70 cell line was more 5-FU resistant than the KYSE450 cell line and such 5-FU resistance is correlated to Notch1 expression verified by Notch1 knockdown experiments. In clinical samples, Notch1 protein expression was detected in the basal cells of human esophagus epithelia, and its expression in squamous cell carcinomas was significantly associated with higher pathological grade and shorter overall survival. We conclude that Notch1 expression is associated with cell aggressiveness and 5-FU drug resistance in human esophageal squamous cell carcinoma cell lines in vitro and is significantly associated with a poor survival in human esophageal squamous cell carcinomas.
Insights
Notch1 expression in esophageal squamous cell carcinoma is linked to increased aggressiveness and resistance to 5-FU chemotherapy. Higher Notch1 levels correlate with poor patient survival, highlighting its role in cancer progression.
Area of Science:
- Oncology
- Molecular Biology
- Cell Signaling
Background:
- Notch signaling is crucial for normal cell functions, including stem cell maintenance.
- Its role in cancer stem cells suggests involvement in oncogenesis.
- Esophageal squamous cell carcinoma (ESCC) is a significant global health concern.
Purpose of the Study:
- To investigate the expression and role of Notch family members, particularly Notch1, in ESCC.
- To determine the correlation between Notch1 expression, tumor differentiation, drug resistance, and patient survival.
Main Methods:
- Quantitative RT-PCR to assess Notch gene expression in ESCC cell lines and a control cell line.
- Western blot analysis to evaluate Notch1 protein levels.
- Hypoxia induction experiments.
- 5-Fluorouracil (5-FU) resistance assays.
- Notch1 knockdown experiments.
- Immunohistochemical analysis of Notch1 in clinical ESCC samples.
Main Results:
- Higher Notch1 and Notch3 expression was observed in ESCC cell lines compared to normal esophageal epithelial cells.
- Poorly differentiated KYSE70 cells showed high, hypoxia-inducible Notch1 expression, while well-differentiated KYSE450 cells were negative for Notch1.
- KYSE70 cells exhibited greater 5-FU resistance, which was linked to Notch1 expression.
- Clinical ESCC samples showed Notch1 expression associated with higher pathological grade and shorter overall survival.
Conclusions:
- Notch1 expression is associated with increased cell aggressiveness and 5-FU drug resistance in ESCC cell lines.
- Notch1 is a potential biomarker for poor prognosis in patients with esophageal squamous cell carcinoma.
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