AKR1B10 accelerates the production of proinflammatory cytokines via the NF-κB signaling pathway in colon cancer

被引:0
|
作者
Cong Liu
Lei Shi
Wanyun Li
Zilan Huang
Shengyu Wang
Peilan Xu
Tingting Li
Zhenyu Li
Fanghong Luo
Wengang Li
Jianghua Yan
Ting Wu
机构
[1] Xiamen University,Cancer Research Center, School of Medicine
[2] Xiamen University,Department of Basic Medicine, School of Medicine
来源
Journal of Molecular Histology | 2022年 / 53卷
关键词
AKR1B10; Inflammatory cytokine; Colon cancer; Clinicopathological features; Cell proliferation;
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中图分类号
学科分类号
摘要
Aldo–keto reductase family one, member B10 (AKR1B10) has been reported to be involved in the tumorigenesis of various cancers. It has been reported that colorectal cancer is closely associated with chronic inflammation, but the underlying molecular mechanisms are still elusive. In our study, we evaluated the relationship between AKR1B10 expression and clinicopathological characteristics of colon cancer and showed that AKR1B10 expression was significantly correlated with the T stage and clinical stage of colon cancer. Knockdown of AKR1B10 significantly decreased the expression of the inflammatory cytokines IL1α and IL6 induced by lipopolysaccharide by inhibiting the NF-κB signaling pathway. Furthermore, AKR1B10 depends on its reductase activity to affect the NF-κB signaling pathway and subsequently affect the production of inflammatory cytokines. In addition, knockdown of AKR1B10 effectively reduced cell proliferation and clonogenic growth, indicating the biological role of AKR1B10 in colon cancer. Together, our findings provide important insights into a previously unrecognized role of AKR1B10 in colon cancer.
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页码:781 / 791
页数:10
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