Sains Malaysiana 46(9)(2017): 1499–1503
http://dx.doi.org/10.17576/jsm-2017-4609-19
Role
of Cytochrome P450 Monooxygenase in the Bioactivation of Aflatoxin B1
(Peranan
Sitokrom P450 Monooksigenase dalam Biopengaktifan Aflatoksin B1)
SUREEPORN NUALKAEW, HIRUN SAELIM, DANAI TIWAWECH, TANATE PANRAT IMRAN PARVEZ
& AMORNRAT PHONGDARA*
Center for Genomics and
Bioinformatics Research, Department of Molecular Biotechnology
and Bioinformatics, Faculty
of Science, Prince of Songkla University, Hatyai,
Songkhla 90112, Thailand
Received: 31 August
2016/Accepted: 17 January 2017
ABSTRACT
In a previous study, the gene EgP450
that encodes the proteins of 505 amino acids was isolated from oil palm. The
recombinant protein EgP450 is bound to phenylurea-like herbicides which
detoxify the substance. Aflatoxin B1 (AFB1), a mycotoxin produced by Aspergillus sp., is another toxic compound that is known to cause acute toxic effects
and act as a hepatocarcinogenic agent. This study aimed to examine the role of
EgP450 enzyme in mycotoxin bioactivation in human mesenchymal stem cells
(hMSCs). Docking analysis showed that EgP450 is bound to the group of
carcinogens, which includes AFB1, n-(2-fluorenyl) acetamide,
n-n-butyl-n-butan-4-ol-nitrosamine, n-nitrosodiethylamine,
n-nitrosodiethylamine and n-nitrosodimethylamine. An in vivo aflatoxin
toxicity test on hMSCs and AFB1 induces the expression of
Bmi-1 which is one of the markers for the development of cancer. The presence
of EgP450 at 0.15 μg/mL could reduced the Bmi-1 expression in AFB1 induced
cells. Moreover, this protein also showed some antioxidant activity. These
results exhibited the enormous potential of EgP450 in the detoxification
processes.
Keywords: Carcinogen; cytochrome
P450 monooxygenase; detoxification
ABSTRAK
Dalam kajian sebelum ini, gen EgP450
yang mengekod 505 protein asid amino telah dipencilkan daripada kelapa sawit.
Protein rekombinan EgP450 terikat kepada racun herba seperti phenylurea yang
menyahtoksin bahan. Aflatoksin B1 (AFB1), mikotoksin yang dihasilkan
oleh Aspergillus sp., adalah satu lagi toksik sebatian yang diketahui
menyebabkan kesan toksik akut dan bertindak sebagai agen hepatokarsinogen.
Kajian ini bertujuan untuk meneliti peranan enzim EgP450 dalam
biopengaktifan mikotoksin sel stem mesenkim manusia (hMSCs). Analisis dok
menunjukkan bahawa EgP450 terikat kepada kumpulan karsinogen, termasuk AFB1,
n-(2-fluorenil) asetamid, n-n-butil-n-butan-4-ol-nitrosamin,
n-nitrosodietilamin, n-nitrosodietilamin dan n-nitrosodimetilamin. Ujian in
vivo ketoksikan aflatoksin ke atas hMSCs dan AFB1 mengaruh
ekspresi Bmi-1 yang merupakan salah satu penanda bagi pembangunan kanser.
Kehadiran EgP450 pada 0.15 μg/mL boleh mengurangkan ekspresi Bmi-1
dalam sel aruhan AFB1. Selain itu, protein ini juga menunjukkan
beberapa aktiviti antioksidan. Keputusan ini menunjukkan potensi besar EgP450
dalam proses penyahtoksikan.
Kata
kunci: Karsinogen; penyahtoksikan; sitokrom P450 monooksigenase
REFERENCES
Aoyama, T., Yamano, S.,
Guzelian, E.S., Gelhoin, H.V. & Gonzales, E.J. 1990. Five of 12 forms of
vaccinia virus-expressed human hepatic cytochrome P450 metabolically activate
aflatoxin B1. Proceedings of the National Academy of Sciences 87:
4790-4793.
Bulatao-Jayme, J.,
Almero, E.M., Castro, M.C., Jardeleza, M.T. & Salamat, L.A. 1982. A
case-control dietary study of primary liver cancer risk from aflatoxin
exposure. International Journal of Epidemiology 11(2): 112-119.
Crespi, C.L., Penman,
B.W., Steimel, D.T., Gelboin, H.V. & Gonzalez, E.J. 1991. The development
of a human cell line stably expressing human CYP3A4: Role in the metabolic
activation of aflatoxin B1 and comparison to CYP1A2 and CYP2A3. Carcinogenesis 12(2): 255-259.
Gallagher, E.P., Kunze,
K.L., Stapleton, P.L. & Eaton, D.L. 1996. The kinetics of aflatoxin B1
oxidation by human cDNA-expressed and human liver microsomal cytochromes P450
1A2 and 3A4. Toxicology and Applied Pharmacology 141(2): 595-606.
Gallagher, E.P.,
Wienkers, L.C., Stapleton, P.L., Kunze, K.L. & Eaton, D.L. 1994. Role of
human microsomal and human complementary DNA-expressed cytochromes P4501A2 and
P4503A4 in the bioactivation of aflatoxin B1. Cancer Research 54(1):
101-108.
Groopman, D., Cain, L.G.
& Kensler, T. 1988. Aflatoxin exposure in human populations: Measurements
and relationship to cancer. Critical Reviews in Toxicology 19(2):
113-143.
Guengerich, F.P.,
Johnson, W.W., Shimada, T., Ueng, Y.F., Yamazaki, H. & Langouët, S. 1998.
Activation and detoxication of aflatoxin B1. Mutation Research 402(1&2):
121-128.
He, X.Y., Tang, L.,
Wang, S.L., Cai, Q.S., Wang, J.S. & Hong, J.Y. 2006. Efficient activation
of aflatoxin B1 by cytochrome P450 2A13, an enzyme predominantly expressed in
human respiratory tract. International Journal of Cancer 118(11):
2665-2671.
Huey, R.,
Morris, G.M., Olson, A.J. & Goodsell, D.S. 2007. A semiempirical free
energy force field with charge-based desolvation. Journal of Computational
Chemistry 28(6): 1145-1152.
Kensler, T.W., Roebuck, B.D., Wogan, G.N. & Groopman,
J.D. 2011. Aflatoxin: A 50-year odyssey of mechanistic and translational
toxicology. Toxicological Sciences 120(S1): S28-S48.
Lee, P.H., Kuo, K.L.,
Chu, P.Y., Liu, E.M. & Lin, J.H. 2009. SLITHER: A web server for generating
contiguous conformations of substrate molecules entering into deep active sites
of proteins or migrating through channels in membrane transporters. Nucleic
Acids Research 37: W559-W564.
Livak, K.J. &
Schmittgen, T.D. 2001. Analysis of relative gene expression data using real-
time quantitative PCR and the 2-ΔΔCT. Methods 25(4): 402-408.
Mihara, K., Chowdhury,
M., Nakaju, N., Hidani, S., Ihara, A., Hyodo, H., Yasunaga, S., Takihara, Y.
& Kimura, A. 2006. Bmi-1 is useful as a novel molecular marker for
predicting progression of myelodysplastic syndrome and prognosis of the
patients. Blood 107(1): 305-308.
Morris, G.M., Goodsell,
D.S., Huey, R. & Olson, A.J. 1996. Distributed automated docking of
flexible ligands - to proteins: Parallel applications of AutoDock 2.4. Journal
of Computer-Aided Molecular Design 10(4): 293-304.
Peers, E., Bosch, X.,
Kaldor, J., Linsell, A. & Pluumen, M. 1987. Aflatoxin exposure, hepatitis B
virus infection and liver cancer in Swaziland. International Journal of
Cancer 39(5): 545-553.
Peers, E. & Linsell,
C.A. 1973. Dietary aflatoxins and liver cancer-a population based study in
Kenya. British Journal of Cancer 27(6): 473-483.
Phongdara, A., Nakkaew,
A. & Nualkaew, S. 2012. Isolation of the detoxification enzyme EgP450 from
an oil palm EST library. Pharmaceutical Biology 50(1): 120-127.
Portman, R.S., Plowman,
K.M. & Campbell, T.C. 1970. On mechanisms affecting species susceptibility
to aflatoxin. Biochimica et Biophysica Acta 208(3): 487-495.
Ramsdell, H.S.,
Parkinson, A., Eddy, A.C. & Eaton, D.L. 1991. Bioactivation of aflatoxin B1
by human liver microsomes: Role of cytochrome P450 IIIA enzymes. Toxicology
and Applied Pharmacology 108(3): 436-447.
Raney, K.D., Shimada,
T., Kim, D-H., Groopman, J.D., Harris, T.M. & Guengerich, F.P. 1992.
Oxidation of aflatoxins and sterigmatocystin by human liver microsomes:
Significance of aflatoxin-Q1 as a detoxication product of aflatoxin-B1. Chemical
Research in Toxicology 5(2): 202-210.
Shimada, T. &
Guengedch, E.E. 1989. Evidence for cytochrome P-450NF, the nifedipine oxidase,
being the principal enzyme involved in the bioactivation of aflatoxins in human
liver. Proceedings of the National Academy of Sciences 86(2): 462-465.
Song, L.B., Zeng, M.S.,
Liao, W.T., Zhang, L., Mo, H.Y., Liu, W.L., Shao, J.Y., Wu, Q.L., Li, M.Z.,
Xia, Y.F., Fu, L.W., Huang, W.L., Dimri, G.P., Band, V. & Zeng, Y.X. 2006.
Bmi- 1 is a novel molecular marker of nasopharyngeal carcinoma progression and
immortalizes primary human nasopharyngeal epithelial cells. Cancer Research 66(12):
6225-6232.
Vesselinovitch, S.D., Mihailovich,
N., Wogan, G.N., Lombard, L.S. & Rao, K.V.N. 1972. Aflatoxin B1, a
hepatocarcinogen in the infant mouse. Cancer Research 32: 2289-2291.
Vieira, P.M., Francisco,
A.F., Souza, S.M., Malaquias, L.C., Reis, A.B., Giunchetti, R.C., Veloso, V.M.,
de Lana, M., Tafuri, W.L. & Carneiro, C.M. 2009. Trypanosoma cruzi: Serum
levels of nitric oxide and expression of inducible nitric oxide synthase in
myocardium and spleen of dogs in the acute stage of infection with metacyclic
or blood trypomastigotes. Experimental Parasitology 121(1): 76-82.
Wogan, G.N. 1973. Host
environment interactions in the etiology of cancer in man. Cancer Research 7:
237-241.
*Corresponding author; email: pamornra@yahoo.com