NAD(P)H dehydrogenase (quinone 1)

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NAD(P)H dehydrogenase, quinone 1
Protein NQO1 PDB 1d4a.png
PDB rendering based on 1d4a.
Available structures
PDB Ortholog search: PDBe, RCSB
External IDs OMIM125860 MGI103187 HomoloGene695 ChEMBL: 3623 GeneCards: NQO1 Gene
EC number
RNA expression pattern
PBB GE NQO1 201468 s at tn.png
PBB GE NQO1 201467 s at tn.png
PBB GE NQO1 210519 s at tn.png
More reference expression data
Species Human Mouse
Entrez 1728 18104
Ensembl ENSG00000181019 ENSMUSG00000003849
UniProt P15559 Q64669
RefSeq (mRNA) NM_000903 NM_008706
RefSeq (protein) NP_000894 NP_032732
Location (UCSC) Chr 16:
69.71 – 69.73 Mb
Chr 8:
107.39 – 107.4 Mb
PubMed search [1] [2]

NAD(P)H dehydrogenase [quinone] 1 is an enzyme that in humans is encoded by the NQO1 gene.[1] This protein-coding gene is a member of the NAD(P)H dehydrogenase (quinone) family and encodes a 2-electron reductase (enzyme). This FAD-binding protein forms homodimers and performs two-electron reduction of quinones to hydroquinones and of other redox dyes. It has a preference for short-chain acceptor quinones, such as ubiquinone, benzoquinone, juglone and duroquinone.[2] This gene has an important paralog NQO2. This protein is located in the cytosol.[3]

NQO1 enzyme expression can be induced by dioxin[4] and inhibited by dicoumarol.[5]


This gene is a member of the NAD(P)H dehydrogenase (quinone) family and encodes a cytoplasmic 2-electron reductase. This FAD-binding protein forms homodimers and reduces quinones to hydroquinones. This protein's enzymatic activity prevents the one electron reduction of quinones that results in the production of radical species.[6]

The ubiquitin-independent p53 degradation pathway is regulated by NQO1. NQO1 stabilizes p53, protecting it from degradation. Individuals with decreased NQO1 expression/activity have reduced p53 stability, which may lead to resistance to drugs such as chemotherapeutics.[7]


Quinonoid compounds generate reactive oxygen species (ROS) via redox cycling mechanisms and arylating nucleophiles. NQO1 is employed in the removal of a quinone from biological systems as a detoxification reaction:  NAD(P)H + a quinone → NAD(P)+ + a hydroquinone.  This reaction ensures complete oxidation of the substrate without the formation of semiquinones and species with reactive oxygen radicals that are deleterious to cells. The localization of NQO1 in epithelial and endothelial tissues of mice, rats and humans indicates their importance in detoxifying agent, since their location facilitates exposure to compounds entering the body.

Vitamin K metabolism[edit]

The enzyme is also involved in biosynthetic processes such as the vitamin K-dependent gamma-carboxylation of glutamate residues in prothrombin synthesis.[8] NQO1 catalyzes the reduction of vitamin K1,K2 and K3 into their hydroquinone form, but it only has a high affinity for Vitamin K3. Vitamin K hydroquinone serves as a cofactor for vitamin K γ‐carboxylase that catalyzes γ‐carboxylation of specific glutamic acid residues in Gla‐factors/proteins (Gla domain) leading to their activation and participation in blood clotting and bone metabolism. Vitamin K is used as radiation sensitizer or in mixtures with other chemotherapeutic drugs to treat several types of cancer. ROS generated in redox cycling contributes to anticancer activity of vitamin K. NQO1 competes with enzymes that redox cycle vitamin K to formation of semiquinone and ROS. NQO1is therefore able to detoxify vitamin K3 and protect cells against oxidative stress.[9]

Bioactivation of antitumor agents[edit]

Several anti-tumor agents such as mitosenes, indolequinones, aziridinylbenzoquinones and β-lapachonehave been designed be bioactivated by NQO1. The high levels of NQO1 expression in many human solid tumors compared to normal tissue ensures their selective activation within tumor cells.[10][11]

Reduction of endogenous quinones[edit]

NQO1 plays a role in ubiquinone and vitamin E quinone metabolism. These quinones protect cellular membranes from peroxidative injury in their reduced state. Furthermore, reduced forms of ubiquinone and vitamin E quinone have been shown to possess antioxidant properties that are superior to their non-reduced forms.[12]



One widespread single-nucleotide polymorphism of the NQO1 gene (NQO1*2), found homozygous in 4% to 20% of different populations, has found to be connected with different forms of cancer and a lowered efficiency of some chemotherapeutics like mitomycin C. This single nucleotide polymorphism leads to a proline serine exchange on position 187. NAD(P)H dehydrogenase [quinone] 1 P187S has been shown to have a lowered activity and stability. Crystallographic and nuclear magnetic resonance data show that the reason for this different behaviour is found in a flexible C-terminus of the protein leading to a destabilization of the whole protein.[13] Recent pharmacological research suggests feasibility of genotype-directed redox chemotherapeutic intervention targeting NQO1*2 breast cancer.[14]


One further single nucleotide polymorphism, found homozygous in 0% to 5% of different ethnic population, is leading to an amino acid exchange on position 139 from arginine to tryptophane.[15] Furthermore an alternative RNA splicing site is created leading to a loss of the quinone binding site.[16] The variant protein of NQO1*3 has similar stability as its wild-type counterpart. The variation between the two is substrate specific and it has reduced activity for some substrates.[17] It has been recently shown that the NQO1*3 polymorphism may also lead to reduced NQO1 protein expression.[18]


NAD(P)H dehydrogenase (quinone 1) has been shown to interact with HSPA4,[19] p53, p33 and p73.[13]

Regulation by Keap1/Nrf2/ARE pathway[edit]

External (via chemicals) and internal (stress response or caloric restriction) induction of NQO1 is mediated solely through the Keap1/Nrf2/ARE. Keap1 acts as the sensor which loses its ability to target Nrf2 for degradation upon exposure to the inducers. Nrf2 is consequently stabilized and accumulated in the nucleus upon which it binds to the AREs and initiates expression of cytoprotective genes including NQO1.[20]

p53 and p73[edit]

p53 and p73 are tumor suppressor proteins and their degradation is tightly regulated by ubiquitination. Recently it was shown that their degradation can also occur via an ubiquitin-independent process;[21] NQO1 blocks p53 and p73 degradation in the presence of NADH and protects them from 20S proteasomal degradation. This protein-protein interaction between p53 and NQO1 was non-catalytic.[22]

Ornithine decarboxylase[edit]

Ornithine decarboxylase (ODC), is a labile protein that is the first rate-limiting enzyme in polyamine biosynthesis. Its degradation is regulated by antizyme that is induced by polyamine production. NQO1 has been shown to stabilze the degradation of ODC by binding to it and protecting it from 20S proteasomal degradation.

Clinical significance[edit]

Mutations in this gene have been associated with tardive dyskinesia (TD), an increased risk of hematotoxicity after exposure to benzene, and susceptibility to various forms of cancer. Altered expression of this protein has been seen in many tumors and is also associated with Alzheimer's disease (AD).[6]

Benzene toxicity[edit]

Benzene poisoning can increase risk of hematological cancers and other disorders. The mechanism of benzene metabolism and how it affects toxicity has not been completely understood. A general observation is that there is high variation in the extent of damage due to benzene poisoning. A possible explanation is the accumulation of phenols and hydroquinone in the target organ—the bone marrow—and subsequent oxidation of these metabolites to reactive quinone metabolites via a number of possible pathways.[18] A case-control study conducted in China showed that patients with two copies of the NQO1 C609T (NQO1*2 polymorphism) mutation had a 7.6-fold increased risk of benzene poisoning compared to those who carried one or two wild-type NQO1 alleles.[23]

Alzheimer's disease[edit]

Oxidative stress been linked to onset of Alzheimer's disease (AD)[24] Since the NQO1*2 polymorphism affects the NQO1 activity and hence increase in oxidative stress, it has been postulated that this might increase the susceptibility of affected subjects for developing AD. A study conducted with a Chinese population consisting of 104 LOAD patients and 128 control patients disproved this hypothesis.[25]


Several studies have been conducted to prove relationship between NQO1 polymorphism and susceptibility to cancer. However, the results have been heterogeneous and inconclusive. Following these studies, meta-analyses have been performed to examine the association between NQO1 polymorphism and increased cancer risk. The results from some of these analyses have been summarized in the table below:

Cancer Type Polymorphism Risk Odds Ratio (95% Confidence Interval) Reference
Prostate C609T All ethnicities: No significant change

Asians: 1.419 (1.1053-1.913)

Acute Lymphoblastic Leukemia C609T All ethnicities: 1.46 (1.18-1.79)

Non-Asians 1.74 (1.29-2.36)

Breast C609T All ethnicities: No significant change

Caucasians: 1.177 (1.041-1.331)

Colorectal C609T All ethnicities: 1.34 (1.10-1.64) [29]
Bladder C609T All ethnicities: 1.18 (1.06-1.31) [30]
De novo childhood leukemia C609T All ethnicities: 1.58 (1.22-2.07)

Europeans, Asians: 1.52 (1.05-2.19)
English, Japanese: No significant change



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  14. ^ Cabello CM, Lamore SD, Bair WB, Davis AL, Azimian SM, Wondrak GT (2011). "DCPIP (2,6-dichlorophenolindophenol) as a genotype-directed redox chemotherapeutic targeting NQO1*2 breast carcinoma". Free Radic. Res. 45 (3): 276–292. doi:10.3109/10715762.2010.526766. PMID 21034357. 
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  19. ^ Anwar A, Siegel D, Kepa JK, Ross D (2002). "Interaction of the molecular chaperone Hsp70 with human NAD(P)H:quinone oxidoreductase 1". J. Biol. Chem. 277 (16): 14060–7. doi:10.1074/jbc.M111576200. PMID 11821413. 
  20. ^ Dinkova-Kostova AT, Holtzclaw WD, Cole RN, Itoh K, Wakabayashi N, Katoh Y, Yamamoto M, Talalay P (Sep 2002). "Direct evidence that sulfhydryl groups of Keap1 are the sensors regulating induction of phase 2 enzymes that protect against carcinogens and oxidants". Proceedings of the National Academy of Sciences of the United States of America 99 (18): 11908. doi:10.1073/pnas.172398899. PMID 12193649. 
  21. ^ Asher G, Tsvetkov P, Kahana C, Shaul Y (Feb 2005). "A mechanism of ubiquitin-independent proteasomal degradation of the tumor suppressors p53 and p73". Genes & Development 19 (3): 316. doi:10.1101/gad.319905. PMID 15687255. 
  22. ^ Asher, G; Bercovich, Z; Tsvetkov, P; Shaul, Y; Kahana, C (2005). "20S proteasomal degradation of ornithine decarboxylase is regulated by NQO1". Molecular Cell 17 (5): 645–55. doi:10.1016/j.molcel.2005.01.020. PMID 15749015. 
  23. ^ Rothman N, Smith MT, Hayes RB, Traver RD, Hoener B, Campleman S, Li GL, Dosemeci M, Linet M, Zhang L, Xi L, Wacholder S, Lu W, Meyer KB, Titenko-Holland N, Stewart JT, Yin S, Ross D (Jul 1997). "Benzene poisoning, a risk factor for hematological malignancy, is associated with the NQO1 609C-->T mutation and rapid fractional excretion of chlorzoxazone". Cancer Research 57 (14): 2839–42. PMID 9230185. 
  24. ^ Miranda S, Opazo C, Larrondo LF, Muñoz FJ, Ruiz F, Leighton F, Inestrosa NC (Dec 2000). "The role of oxidative stress in the toxicity induced by amyloid beta-peptide in Alzheimer's disease". Progress in Neurobiology 62 (6): 633. doi:10.1016/S0301-0082(00)00015-0. PMID 10880853. 
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  26. ^ Sun Z, Cui Y, Pei J, Fan Z (Aug 2014). "Association between NQO1 C609T polymorphism and prostate cancer risk". Tumour Biology 35 (8): 7993–8. doi:10.1007/s13277-014-2051-5. PMID 24838947. 
  27. ^ Li C, Zhou Y (Jun 2014). "Association between NQO1 C609T polymorphism and acute lymphoblastic leukemia risk: evidence from an updated meta-analysis based on 17 case-control studies". Journal of Cancer Research and Clinical Oncology 140 (6): 873–81. doi:10.1007/s00432-014-1595-5. PMID 24488035. 
  28. ^ Peng Q, Lu Y, Lao X, Chen Z, Li R, Sui J, Qin X, Li S (2014). "The NQO1 Pro187Ser polymorphism and breast cancer susceptibility: evidence from an updated meta-analysis". Diagnostic Pathology 9: 100. doi:10.1186/1746-1596-9-100. PMC 4041044. PMID 24884893. 
  29. ^ Zheng B, Wang Z, Chai R (Aug 2014). "NQO1 C609T polymorphism and colorectal cancer susceptibility: a meta-analysis". Archives of Medical Science 10 (4): 651–60. doi:10.5114/aoms.2014.44856. PMC 4175766. PMID 25276147. 
  30. ^ Gong M, Yi Q, Wang W (Oct 2013). "Association between NQO1 C609T polymorphism and bladder cancer susceptibility: a systemic review and meta-analysis". Tumour Biology 34 (5): 2551–6. doi:10.1007/s13277-013-0799-7. PMID 23749485. 
  31. ^ Yang FY, Guan QK, Cui YH, Zhao ZQ, Rao W, Xi Z (Sep 2012). "NAD(P)H quinone oxidoreductase 1 (NQO1) genetic C609T polymorphism is associated with the risk of digestive tract cancer: a meta-analysis based on 21 case-control studies". European Journal of Cancer Prevention 21 (5): 432–41. doi:10.1097/CEJ.0b013e32834f7514. PMID 22387672. 

Further reading[edit]

  • Vasiliou V, Ross D, Nebert DW (2006). "Update of the NAD(P)H:quinone oxidoreductase (NQO) gene family". Hum. Genomics 2 (5): 329–35. doi:10.1186/1479-7364-2-5-329. PMID 16595077. 
  • Li Y, Jaiswal AK (1992). "Regulation of human NAD(P)H:quinone oxidoreductase gene. Role of AP1 binding site contained within human antioxidant response element". J. Biol. Chem. 267 (21): 15097–104. PMID 1340765. 
  • Jaiswal AK (1991). "Human NAD(P)H:quinone oxidoreductase (NQO1) gene structure and induction by dioxin". Biochemistry 30 (44): 10647–53. doi:10.1021/bi00108a007. PMID 1657151. 
  • Traver RD, Horikoshi T, Danenberg KD, Stadlbauer TH, Danenberg PV, Ross D, Gibson NW (1992). "NAD(P)H:quinone oxidoreductase gene expression in human colon carcinoma cells: characterization of a mutation which modulates DT-diaphorase activity and mitomycin sensitivity". Cancer Res. 52 (4): 797–802. PMID 1737339. 
  • Chen LZ, Harris PC, Apostolou S, Baker E, Holman K, Lane SA, Nancarrow JK, Whitmore SA, Stallings RL, Hildebrand CE (1991). "A refined physical map of the long arm of human chromosome 16". Genomics 10 (2): 308–12. doi:10.1016/0888-7543(91)90313-4. PMID 2071140. 
  • Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene 138 (1-2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298. 
  • Rothman N, Smith MT, Hayes RB, Traver RD, Hoener B, Campleman S, Li GL, Dosemeci M, Linet M, Zhang L, Xi L, Wacholder S, Lu W, Meyer KB, Titenko-Holland N, Stewart JT, Yin S, Ross D (1997). "Benzene poisoning, a risk factor for hematological malignancy, is associated with the NQO1 609C-->T mutation and rapid fractional excretion of chlorzoxazone". Cancer Res. 57 (14): 2839–42. PMID 9230185. 
  • Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, Suyama A, Sugano S (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene 200 (1-2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149. 
  • Smiley JF, Levey AI, Mesulam MM (1998). "Infracortical interstitial cells concurrently expressing m2-muscarinic receptors, acetylcholinesterase and nicotinamide adenine dinucleotide phosphate-diaphorase in the human and monkey cerebral cortex". Neuroscience 84 (3): 755–69. doi:10.1016/S0306-4522(97)00524-1. PMID 9579781. 
  • Moran JL, Siegel D, Ross D (1999). "A potential mechanism underlying the increased susceptibility of individuals with a polymorphism in NAD(P)H:quinone oxidoreductase 1 (NQO1) to benzene toxicity". Proc. Natl. Acad. Sci. U.S.A. 96 (14): 8150–5. doi:10.1073/pnas.96.14.8150. PMC 22203. PMID 10393963. 
  • Kristiansen OP, Larsen ZM, Johannesen J, Nerup J, Mandrup-Poulsen T, Pociot F (1999). "No linkage of P187S polymorphism in NAD(P)H: quinone oxidoreductase (NQO1/DIA4) and type 1 diabetes in the Danish population. DIEGG and DSGD. Danish IDDM Epidemiology and Genetics Group and The Danish Study Group of Diabetes in Childhood". Hum. Mutat. 14 (1): 67–70. doi:10.1002/(SICI)1098-1004(1999)14:1<67::AID-HUMU8>3.0.CO;2-5. PMID 10447260. 
  • Eliasson M, Boström M, DePierre JW (1999). "Levels and subcellular distributions of detoxifying enzymes in the ovarian corpus luteum of the pregnant and non-pregnant pig". Biochem. Pharmacol. 58 (8): 1287–92. doi:10.1016/S0006-2952(99)00185-9. PMID 10487530. 
  • Skelly JV, Sanderson MR, Suter DA, Baumann U, Read MA, Gregory DS, Bennett M, Hobbs SM, Neidle S (1999). "Crystal structure of human DT-diaphorase: a model for interaction with the cytotoxic prodrug 5-(aziridin-1-yl)-2,4-dinitrobenzamide (CB1954)". J. Med. Chem. 42 (21): 4325–30. doi:10.1021/jm991060m. PMID 10543876. 
  • Faig M, Bianchet MA, Talalay P, Chen S, Winski S, Ross D, Amzel LM (2000). "Structures of recombinant human and mouse NAD(P)H:quinone oxidoreductases: species comparison and structural changes with substrate binding and release". Proc. Natl. Acad. Sci. U.S.A. 97 (7): 3177–82. doi:10.1073/pnas.050585797. PMC 16212. PMID 10706635. 
  • Harada S, Fujii C, Hayashi A, Ohkoshi N (2001). "An association between idiopathic Parkinson's disease and polymorphisms of phase II detoxification enzymes: glutathione S-transferase M1 and quinone oxidoreductase 1 and 2". Biochem. Biophys. Res. Commun. 288 (4): 887–92. doi:10.1006/bbrc.2001.5868. PMID 11688992. 
  • Siegel D, Ryder J, Ross D (2001). "NAD(P)H: quinone oxidoreductase 1 expression in human bone marrow endothelial cells". Toxicol. Lett. 125 (1-3): 93–8. doi:10.1016/S0378-4274(01)00426-X. PMID 11701227. 
  • Anwar A, Siegel D, Kepa JK, Ross D (2002). "Interaction of the molecular chaperone Hsp70 with human NAD(P)H:quinone oxidoreductase 1". J. Biol. Chem. 277 (16): 14060–7. doi:10.1074/jbc.M111576200. PMID 11821413. 
  • Winski SL, Koutalos Y, Bentley DL, Ross D (2002). "Subcellular localization of NAD(P)H:quinone oxidoreductase 1 in human cancer cells". Cancer Res. 62 (5): 1420–4. PMID 11888914. 
  • Begleiter A, Lange L (2002). "Lack of NQO1 induction in human tumor cells is not due to changes in the promoter region of the gene". Int. J. Oncol. 20 (4): 835–8. doi:10.3892/ijo.20.4.835. PMID 11894133. 

This article incorporates text from the United States National Library of Medicine, which is in the public domain.