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Updated: Jul 22, 2025

Development of Compendium for Esophageal Squamous Cell Carcinoma
Published on: April 12, 2024
Curcumin inhibits esophageal squamous cell carcinoma progression through down-regulating the circNRIP1/miR-532-3p/AKT
Tianxia Luo1, Hongya Guan2, Jia Liu3
1Department of Physiology, School of Medicine, Henan University of Chinese Medicine, Zhengzhou, China.
Abstract:
Curcumin shows an anti-cancer role in many kinds of tumors. However, the mechanism of its anti-tumor function in esophageal squamous cell carcinoma (ESCC) remains largely unknown. Herein, we explored the therapeutic potential of curcumin for esophageal cancer. Curcumin could time- and dose-dependently inhibit ESCC cells activity. Additionally, ESCC cells exposed to 20 μM of curcumin exhibited significantly decreased proliferative and invasive capacities, as well as enhanced cell apoptosis. ESCC tissues and cells exhibited significantly increased circNRIP1 expression when compared to their counterparts. circNRIP1 knockdown markedly impaired cell proliferation, clone formation, cell migration and invasion but promoted apoptosis. Exposure to 10-20 μM of curcumin inhibited circNRIP1 expression, however, overexpression of circNRIP1 could significantly restored the biological characteristics that were inhibited by curcumin exposure in vivo and in vitro. circNRIP1 promoted the malignancy of ESCC by combining miR-532-3p, and downstream AKT3. Curcumin inhibited AKT phosphorylation by up-regulating miR-532-3p expression, thereby inhibiting the activation of the AKT pathway. In summary, curcumin is a potent inhibitor of ESCC growth, which can be achieved through the regulation of the circNRIP1/miR-532-3p/AKT pathway. This research may provide new mechanisms for curcumin to inhibit the malignant development of ESCC.
Insights
Curcumin effectively inhibits esophageal squamous cell carcinoma (ESCC) growth by downregulating circNRIP1 expression. This natural compound targets the circNRIP1/miR-532-3p/AKT pathway, offering a potential therapeutic strategy for ESCC.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Curcumin exhibits anti-cancer properties across various tumors.
- The specific anti-tumor mechanisms of curcumin in esophageal squamous cell carcinoma (ESCC) are not well understood.
Purpose of the Study:
- To investigate the therapeutic potential and underlying mechanisms of curcumin in esophageal cancer.
- To elucidate the role of circNRIP1 in ESCC progression and its interaction with curcumin treatment.
Main Methods:
- In vitro and in vivo experiments assessing curcumin's effects on ESCC cell activity, proliferation, invasion, and apoptosis.
- Analysis of circNRIP1 expression in ESCC tissues and cells.
- Investigating the regulatory pathway involving circNRIP1, miR-532-3p, and AKT3.
Main Results:
- Curcumin dose-dependently inhibited ESCC cell activity, proliferation, and invasion, while promoting apoptosis.
- Increased circNRIP1 expression was observed in ESCC tissues and cells, correlating with malignancy.
- Curcumin suppressed circNRIP1 expression, and circNRIP1 overexpression reversed curcumin's inhibitory effects, highlighting its oncogenic role.
- Curcumin upregulated miR-532-3p, inhibiting AKT phosphorylation and pathway activation, mediated by circNRIP1.
Conclusions:
- Curcumin acts as a potent inhibitor of ESCC growth.
- The circNRIP1/miR-532-3p/AKT pathway is a key mechanism through which curcumin exerts its anti-tumor effects in ESCC.
- This study provides novel insights into curcumin's anti-cancer mechanisms against ESCC, suggesting potential therapeutic applications.
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