Aflatoxin B1 metabolism (WP925)
Pan troglodytes
'''Aflatoxins''' are naturally occurring [[wikipedia:mycotoxin|mycotoxin]]s that are produced by many species of ''[[wikipedia:Aspergillus|Aspergillus]]'', a [[wikipedia:fungus|fungus]], most notably ''[[wikipedia:Aspergillus flavus|Aspergillus flavus]]'' and ''[[wikipedia:Aspergillus parasiticus|Aspergillus parasiticus]]''. After entering the body, aflatoxins are metabolized by the liver to a reactive intermediate, aflatoxin M1, an [[wikipedia:epoxide|epoxide]]. Aflatoxin B1 is considered the most toxic and is produced by both Aspergillus flavus and Aspergillus parasiticus. Source: [[wikipedia:Aflatoxin|Wikipedia]]
Authors
Thomas Kelder , Egon Willighagen , and Christine ChichesterActivity
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Cited In
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Organisms
Pan troglodytesCommunities
Annotations
Pathway Ontology
aflatoxin metabolic pathwayLabel | Type | Compact URI | Comment |
---|---|---|---|
Aflatoxin B1 exo-8,9-epoxide-GSH | Metabolite | pubchem.compound:5460816 | |
Aflatoxin B1 8,9-dihydrodiol | Metabolite | pubchem.compound:3035008 | |
aflatoxin B1 | Metabolite | hmdb:HMDB0006552 | |
Aflatoxin B1 exo-8,9-epoxide | Metabolite | pubchem.compound:104756 | |
Aflatoxin M1 | Metabolite | pubchem.compound:15558498 | |
Aflatoxin Q1 | Metabolite | pubchem.compound:104757 | |
AKR7A2 | GeneProduct | ensembl:ENSPTRG00000000265 | |
Q9N256_PANTR | GeneProduct | ensembl:ENSPTRG00000007281 | |
AKR7A3 | GeneProduct | ensembl:ENSPTRG00000000264 | |
GSTT1 | GeneProduct | ensembl:ENSPTRG00000014166 | |
GSTM1 | GeneProduct | ensembl:ENSPTRG00000001061 | |
XR_022976.1 | GeneProduct | ensembl:ENSPTRG00000002039 | |
B1NL93_PANTR | GeneProduct | ensembl:ENSPTRG00000019460 |
References
- Glutathione S-transferase-catalyzed conjugation of bioactivated aflatoxin B(1) in human lung: differential cellular distribution and lack of significance of the GSTM1 genetic polymorphism. Stewart RK, Smith GB, Donnelly PJ, Reid KR, Petsikas D, Conlan AA, et al. Carcinogenesis. 1999 Oct;20(10):1971–7. PubMed Europe PMC Scholia
- Reduction of aflatoxin B1 dialdehyde by rat and human aldo-keto reductases. Guengerich FP, Cai H, McMahon M, Hayes JD, Sutter TR, Groopman JD, et al. Chem Res Toxicol. 2001 Jun;14(6):727–37. PubMed Europe PMC Scholia
- Role of genetic polymorphism of glutathione-S-transferase T1 and microsomal epoxide hydrolase in aflatoxin-associated hepatocellular carcinoma. Tiemersma EW, Omer RE, Bunschoten A, van’t Veer P, Kok FJ, Idris MO, et al. Cancer Epidemiol Biomarkers Prev. 2001 Jul;10(7):785–91. PubMed Europe PMC Scholia
- Reaction of aflatoxin B(1) oxidation products with lysine. Guengerich FP, Arneson KO, Williams KM, Deng Z, Harris TM. Chem Res Toxicol. 2002 Jun;15(6):780–92. PubMed Europe PMC Scholia
- Translational strategies for cancer prevention in liver. Kensler TW, Qian GS, Chen JG, Groopman JD. Nat Rev Cancer. 2003 May;3(5):321–9. PubMed Europe PMC Scholia
- Efficient activation of aflatoxin B1 by cytochrome P450 2A13, an enzyme predominantly expressed in human respiratory tract. He XY, Tang L, Wang SL, Cai QS, Wang JS, Hong JY. Int J Cancer. 2006 Jun 1;118(11):2665–71. PubMed Europe PMC Scholia
- Cytochrome P450s and other enzymes in drug metabolism and toxicity. Guengerich FP. AAPS J. 2006 Mar 10;8(1):E101-11. PubMed Europe PMC Scholia
- CYP2A13 in human respiratory tissues and lung cancers: an immunohistochemical study with a new peptide-specific antibody. Zhu LR, Thomas PE, Lu G, Reuhl KR, Yang GY, Wang LD, et al. Drug Metab Dispos. 2006 Oct;34(10):1672–6. PubMed Europe PMC Scholia
- Aldo-keto reductases and bioactivation/detoxication. Jin Y, Penning TM. Annu Rev Pharmacol Toxicol. 2007;47:263–92. PubMed Europe PMC Scholia
- The aldo-keto reductase superfamily and its role in drug metabolism and detoxification. Barski OA, Tipparaju SM, Bhatnagar A. Drug Metab Rev. 2008;40(4):553–624. PubMed Europe PMC Scholia