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Updated: May 9, 2026

Development of Compendium for Esophageal Squamous Cell Carcinoma
Published on: April 12, 2024
Characterization of tumor suppressive function of cornulin in esophageal squamous cell carcinoma
Kai Chen1, Yan Li, Yongdong Dai
1State Key Laboratory of Oncology in Southern China, Cancer Center, Sun Yat-Sen University, Guangzhou, China.
Abstract:
By using cDNA microarray analysis, we identified cornulin (CRNN) gene was frequently downregulated in esophageal squamous cell carcinoma (ESCC). In the present study, we investigated the role of CRNN in ESCC development. The results showed that CRNN was frequently downregulated in primary ESCCs in both mRNA level (26/56, 46.4%) and protein level (137/249, 55%), which was significantly associated with lymph node metastases (P=0.027), advanced clinical stage (P=0.039), and overall survival rate (P<0.001). Multivariate analysis indicated that the CRNN downregulation was an independent prognostic factor for ESCC. Functional studies with both in vitro and in vivo assays demonstrated that CRNN had strong tumor suppressive ability in ESCC cells. The tumor-suppressive mechanism of CRNN was associated with its role in cell cycle arrest at G1/S checkpoint by upregulating expressions of P21(WAF1/CIP1) and Rb. Silencing CRNN expression by RNA interference could effectively inhibit its tumor suppressive effect. In conclusion, our findings demonstrate that CRNN is a tumor suppressor gene that plays a critical tumor suppressive role in ESCC.
Insights
Cornulin (CRNN) is frequently downregulated in esophageal squamous cell carcinoma (ESCC), acting as a tumor suppressor. Its reduced expression correlates with poor prognosis, highlighting CRNN as a key factor in ESCC development.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Esophageal squamous cell carcinoma (ESCC) is a significant global health concern.
- Identifying novel tumor suppressor genes is crucial for developing effective therapeutic strategies against ESCC.
Purpose of the Study:
- To investigate the role of the cornulin (CRNN) gene in the development of ESCC.
- To determine the prognostic significance of CRNN expression in ESCC patients.
Main Methods:
- cDNA microarray analysis to identify differentially expressed genes in ESCC.
- Quantitative analysis of CRNN mRNA and protein levels in primary ESCC tissues.
- In vitro and in vivo functional assays to assess CRNN's tumor-suppressive ability.
- RNA interference to silence CRNN expression.
Main Results:
- CRNN was frequently downregulated in ESCC at both mRNA (46.4%) and protein (55%) levels.
- CRNN downregulation significantly correlated with lymph node metastasis, advanced clinical stage, and poorer overall survival.
- CRNN exhibited tumor-suppressive activity by inducing G1/S cell cycle arrest via upregulation of P21(WAF1/CIP1) and Rb.
Conclusions:
- CRNN functions as a tumor suppressor gene in ESCC.
- CRNN downregulation is an independent prognostic factor for ESCC.
- Restoring CRNN expression may offer a therapeutic strategy for ESCC.
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