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

被引:9
|
作者
Liu, Cong [1 ]
Shi, Lei [1 ]
Li, Wanyun [1 ]
Huang, Zilan [1 ]
Wang, Shengyu [1 ]
Xu, Peilan [1 ]
Li, Tingting [1 ]
Li, Zhenyu [1 ]
Luo, Fanghong [1 ]
Li, Wengang [1 ]
Yan, Jianghua [1 ]
Wu, Ting [1 ,2 ]
机构
[1] Xiamen Univ, Sch Med, Canc Res Ctr, Xiangan South Rd, Xiamen 361102, Fujian, Peoples R China
[2] Xiamen Univ, Sch Med, Dept Basic Med, Xiangan South Rd, Xiamen 361000, Peoples R China
基金
中国国家自然科学基金;
关键词
Inflammatory cytokine; Colon cancer; Clinicopathological features; Cell proliferation; COLORECTAL-CANCER; INFLAMMATION; IL-1-ALPHA; LIPOPOLYSACCHARIDE; OVEREXPRESSION; METASTASIS; PRINCIPLES; IL-1-BETA; IMPACT;
D O I
10.1007/s10735-022-10093-7
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
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 IL1 alpha and IL6 induced by lipopolysaccharide by inhibiting the NF-kappa B signaling pathway. Furthermore, AKR1B10 depends on its reductase activity to affect the NF-kappa B 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.
引用
收藏
页码:781 / 791
页数:11
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