Birtwistle Jane, Hayden Rachel E, Khanim Farhat L, Green Richard M, Pearce Claire, Davies Nicholas J, Wake Naomi, Schrewe Heiner, Ride Jonathan P, Chipman James K, Bunce Chris M
School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.
Mutat Res. 2009 Mar 9;662(1-2):67-74. doi: 10.1016/j.mrfmmm.2008.12.010. Epub 2008 Dec 31.
The aldo-keto reductase AKR1C3, has been shown to regulate myelopoiesis via its ability to metabolise prostaglandin D2 (PGD2). Other studies have demonstrated the oxidative activation of polycyclic aromatic hydrocarbon (PAH) procarcinogens by AKR1C3 in cell-free systems. This is the first study that addresses whether AKR1C3 mediates carcinogen activation within intact living cells following manipulation of AKR1C3 by molecular intervention. Quantitative RT-PCR identified AKR1C3 as the predominant AKR1C isoform expressed in acute myeloid leukemia (AML). Exposure of K562 and KG1a myeloid cell lines to the known AKR1C3 substrate 7,12-dimethylbenz(a)anthracene-3,4-dihydrodiol (7,12-DMBA-3,4-diol) resulted in both single strand DNA breaks and oxidative DNA damage as measured using conventional and FPG-modified comet assays respectively. PGD2-keto reductase activity was shown to be correlated with relative AKR1C3 expression and together with quantitative real time PCR was used to validate the RNAi-knockdown of AKR1C3 in K562 cells. Knockdown of AKR1C3 did not alter single strand DNA breaks following 7,12-DMBA-3,4-diol exposure but significantly decreased oxidative DNA damage. A similar interrelationship between AKR1C3 activity and 7,12-DMBA-3,4-diol mediated oxidative DNA damage but not single strand breaks was observed in KG1a cells. Finally, AKR1C3 knockdown also resulted in spontaneous erythroid differentiation of K562 cells. Since K562 cells are a model of AML blast crisis of chronic myeloid leukemia (CML) the data presented here identify AKR1C3 as a novel mediator of carcinogen-induced initiation of leukemia, as a novel regulator of erythroid differentiation and paradoxically as a potential new target in the treatment of CML.
醛酮还原酶AKR1C3已被证明可通过其代谢前列腺素D2(PGD2)的能力来调节骨髓生成。其他研究表明,在无细胞系统中,AKR1C3可使多环芳烃(PAH)前致癌物发生氧化活化。这是第一项通过分子干预操纵AKR1C3后,研究其是否在完整活细胞内介导致癌物活化的研究。定量逆转录聚合酶链反应(RT-PCR)确定AKR1C3是急性髓系白血病(AML)中表达的主要AKR1C亚型。将K562和KG1a髓系细胞系暴露于已知的AKR1C3底物7,12-二甲基苯并(a)蒽-3,4-二氢二醇(7,12-DMBA-3,4-diol),分别使用传统彗星试验和FPG修饰彗星试验检测,结果显示出现了单链DNA断裂和氧化性DNA损伤。PGD2-酮还原酶活性与相对AKR1C3表达相关,并与定量实时PCR一起用于验证K562细胞中AKR1C3的RNA干扰敲低。敲低AKR1C3并没有改变7,12-DMBA-3,4-diol暴露后的单链DNA断裂,但显著降低了氧化性DNA损伤。在KG1a细胞中也观察到AKR1C3活性与7,12-DMBA-3,4-diol介导的氧化性DNA损伤之间存在类似的相互关系,但与单链断裂无关。最后,敲低AKR1C3还导致K562细胞自发红系分化。由于K562细胞是慢性髓系白血病(CML)急性髓系白血病母细胞危象的模型,此处呈现的数据表明AKR1C3是致癌物诱导白血病起始的新型介质、红系分化的新型调节因子,并且反常地是CML治疗中的潜在新靶点。