Relative quantification of the proteomic changes associated with the mycotoxin zearalenone in the H295R steroidogenesis model

被引:14
作者
Busk, Oyvind L. [1 ]
Ndossi, Doreen [2 ]
Verhaegen, Steven [2 ]
Connolly, Lisa [3 ]
Eriksen, Gunnar [4 ]
Ropstad, Erik [2 ]
Sorlie, Morten [1 ]
机构
[1] Norwegian Univ Life Sci, Dept Chem Biotechnol & Food Sci, As, Norway
[2] Norwegian Sch Vet Sci, Oslo, Norway
[3] Queens Univ Belfast, Inst Agrifood & Land Use, Sch Biol Sci, Belfast, Antrim, North Ireland
[4] Natl Vet Inst, Oslo, Norway
关键词
Zearalenone; Mycotoxins; Quantitative proteomics; HUMAN-BREAST-CANCER; C-MYC ONCOGENE; NF-KAPPA-B; CELL-LINE; ALPHA-ZEARALENOL; GENE-EXPRESSION; IN-VIVO; ESTROGEN; IDENTIFICATION; PROTEINS;
D O I
10.1016/j.toxicon.2011.08.015
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Zearalenone (ZEN) is a mycotoxin with endocrine disrupting effects having vast economic implications in e.g. pig farming. Structurally, ZEN resembles 17 beta-estradiol, and thus is able to bind to estrogen receptors (ER) in target cells. Because of this, it is also classified as a non-steroidal estrogen, a phytoestrogen, a mycoestrogen, and a growth promoter. Quantitative proteomic analysis was undertaken using stable-isotope labeling by amino acids in cell culture (SILAC) upon exposure of the steroidogenesis cell model H295R with ZEN to elucidate its effect on protein regulation. ZEN significantly regulated 21 proteins, including proteins with known endocrine disrupting effects and several oncogenes. In addition, network analysis using Ingenuity Pathway Analysis showed that ZEN affected the oxidative phosphorylation pathway and the mitochondrial dysfunction pathway, both previously reported to be involved in endocrine dysfunction. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:533 / 542
页数:10
相关论文
共 75 条
[1]   DNA fragmentation, apoptosis and cell cycle arrest induced by zearalenone in cultured DOK, Vero and Caco-2 cells: prevention by Vitamin E [J].
Abid-Essefi, S ;
Baudrimont, I ;
Hassen, W ;
Ouanes, Z ;
Mobio, TA ;
Anane, R ;
Creppy, EE ;
Bacha, H .
TOXICOLOGY, 2003, 192 (2-3) :237-248
[2]   Identification and characterization of novel human tissue-specific RFX transcription factors [J].
Aftab, Syed ;
Semenec, Lucie ;
Chu, Jeffrey Shih-Chieh ;
Chen, Nansheng .
BMC EVOLUTIONARY BIOLOGY, 2008, 8 (1)
[3]   Zearalenone induces immunotoxicity in mice:: possible protective effects of radish extract (Raphanus sativus) [J].
Ben Salah-Abbes, Jalila ;
Abbes, Samir ;
Houas, Zohra ;
Abdel-Wahhab, Mosaad A. ;
Oueslati, Ridha .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2008, 60 (06) :761-770
[4]   Controlling the false discovery rate in behavior genetics research [J].
Benjamini, Y ;
Drai, D ;
Elmer, G ;
Kafkafi, N ;
Golani, I .
BEHAVIOURAL BRAIN RESEARCH, 2001, 125 (1-2) :279-284
[5]   Mycotoxins [J].
Bennett, JW ;
Klich, M .
CLINICAL MICROBIOLOGY REVIEWS, 2003, 16 (03) :497-+
[6]   Correlation of amplification and overexpression of the c-myc oncogene in high-grade breast cancer:: FISH, in situ hybridisation and immunohistochemical analyses [J].
Blancato, J ;
Singh, B ;
Liu, A ;
Liao, DJ ;
Dickson, RB .
BRITISH JOURNAL OF CANCER, 2004, 90 (08) :1612-1619
[7]   The NF-κB regulatory network [J].
Brasier, Allan R. .
CARDIOVASCULAR TOXICOLOGY, 2006, 6 (02) :111-130
[8]  
CHANG K, 1979, AM J VET RES, V40, P1260
[9]  
Chavany C, 1996, J BIOL CHEM, V271, P4974
[10]   MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification [J].
Cox, Juergen ;
Mann, Matthias .
NATURE BIOTECHNOLOGY, 2008, 26 (12) :1367-1372