Aldo‐keto reductase 1B10 protects human colon cells from DNA damage induced by electrophilic carbonyl compounds. Issue 1 (10th March 2016)

• Record Type: Journal Article
• Authors: Zu, Xuyu; Yan, Ruilan; Pan, Jishen; Zhong, Linlin; Cao, Yu; Ma, Jun; Cai, Chuan; Huang, Dan; Liu, Jianghua; Chung, Fung‐Lung; Liao, Duan‐Fang; Cao, Deliang
• Is Part Of: Molecular carcinogenesis. Volume 56:Issue 1(2017:Jan.)
• Page Start: 118
• Page End: 129
• Publication Date: 2016-03-10
• Subjects: AKR1B10 -- electrophilic carbonyl compounds -- DNA damage -- acrolein‐deoxyguanosine adducts -- colorectal cancer; Carcinogenesis -- Molecular aspects -- Periodicals; 616.994071
• DOI: 10.1002/mc.22477
• Languages: English
• ISSNs: 0899-1987

Abstract

Abstract : Electrophilic carbonyl compounds are highly cytotoxic and genotoxic. Aldo‐keto reductase 1B10 (AKR1B10) is an enzyme catalyzing reduction of carbonyl compounds to less toxic alcoholic forms. This study presents novel evidence that AKR1B10 protects colon cells from DNA damage induced by electrophilic carbonyl compounds. AKR1B10 is specifically expressed in epithelial cells of the human colon, but this study found that AKR1B10 expression was lost or markedly diminished in colorectal cancer, precancerous tissues, and a notable portion of normal adjacent tissues (NAT). SiRNA‐mediated silencing of AKR1B10 in colon cancer cells HCT‐8 enhanced cytotoxicity of acrolein and HNE, whereas ectopic expression of AKR1B10 in colon cancer cells RKO prevented the host cells against carbonyl cytotoxicity. Furthermore, siRNA‐mediated AKR1B10 silencing led to DNA breaks and activation of γ‐H2AX protein, a marker of DNA double strand breaks, particularly in the exposure of HNE (10 μM). In the AKR1B10 silenced HCT‐8 cells, hypoxanthine‐guanine phosphoribosyl transferase (HPRT) mutant frequency increased by 26.8 times at basal level and by 33.5 times in the presence of 10 μM HNE when compared to vector control cells. In these cells, the cyclic acrolein‐deoxyguanosine adducts levels were increased by over 10 times. These findings were confirmed by pharmacological inhibition of AKR1B10 activity by Epalrestat. Taken together, these data suggest that AKR1B10 is a critical protein that protects host cells from DNA damage induced by electrophilic carbonyl compounds. AKR1B10 deficiency in the colon may be an important pathogenic factor in disease progression and carcinogenesis. © 2016 Wiley Periodicals, Inc.