赭曲霉毒素A致癌机制研究进展

刘 静,张红英 综述 张祥宏 审校

武警医学 ›› 2017, Vol. 28 ›› Issue (1) : 95-98.

PDF(599 KB)
PDF(599 KB)
武警医学 ›› 2017, Vol. 28 ›› Issue (1) : 95-98.
综述

赭曲霉毒素A致癌机制研究进展

  • 刘 静1,张红英2 综述 张祥宏3 审校
作者信息 +
文章历史 +

摘要

赭曲霉毒素A(ochratoxin A, OTA)是一种主要由纯绿青霉、碳黑曲霉和赭曲霉产生的真菌毒素,广泛存在于食品、农产品和动物饲料中,因此OTA与人类健康的关系备受关注。研究发现,OTA具有肾毒性、肝毒性、神经毒性、免疫毒性和致畸性[1]。国际癌症研究中心(International Agency for Research on Cancer, IARC)1993年把OTA定为“B级人类可能致癌物”[2]。但是,迄今为止有关OTA的致癌作用机制尚不完全清楚。笔者主要就目前备受关注的OTA致癌机制进行综述。

关键词

赭曲霉毒素A / 致癌机制 / 氧化应激

引用本文

导出引用
刘 静,张红英 综述 张祥宏 审校. 赭曲霉毒素A致癌机制研究进展[J]. 武警医学. 2017, 28(1): 95-98
中图分类号: R114   

参考文献

[1] Internationalprogramme on chemical safety (IPCS), 2001. Safety Evaluation of Certain Mycotoxins in Food, WHO Food Additives Series 47, World Health Organization, Geneva.
[2] International Agency for Research on Cancer.Some Naturally Occurring Substances, Food Items and Constituents, Heterocyclic Aromatic Amines and Mycotoxins[J].Geneva: International Agency for Research on Cancer.IARC Monographs on the Evaluation of Carcinogenic Risks to Humans, 1993, 56: 26-32 .
[3] National Toxicology Program.Toxicology and Carcinogenesis Studies of Ochratoxin A (CAS No. 303-47-9) in F344/N Rats (Gavage Studies).Natl Toxicol Program Tech Rep Ser, 1989, 358:1-142.
[4] DFG, DeutcheForschungsgemeinschaft List of MAK andBAT Values, Commission for the investigation of HealthHazards of chemical compounds in the work area, report no.39, Wiley-VCH, VerlagWeinheim,2003.
[5] Schwartz G G. Hypothesis: Does ochratoxin A cause testicular cancer[J]. Cancer Causes Control, 2002, 13(1): 91-100.
[6] Klaunig J E, Kamendulis L M.The role of oxidative stress in carcinogenesis[J]. Annu Rev Pharmacol Toxicol, 2004, 44: 239-267.
[7] Valko M, Rhodes C J, Monco L J, et al. Free radicals, metals and antioxidants in oxidative stress-induced cancer [J]. Chem Biol Interact, 2006, 160(1): 1-40.
[8] Omar R F, Hasino B B, Mejilla F, et al. Mechanism of ochratoxin a stimulated lipid peroxidation [J]. Biochemical Pharmacology, 1990, 40(6): 1183-1191.
[9] Faucet-Marquis V, Pont F, Stormer F C, et al. Evidence of a new dechlorinatedochratoxin A derivative formed in opossum kidney cell cultures after pretreatment by modulators of glutathione pathways: correlation with DNA-adduct formation [J]. Mol Nutr Food Res, 2006, 50(6): 530-542.
[10] KenslerTW, WakabayashiN, Biswal S. Cell survival responses to environmental stresses via the Keap1-Nrf2-ARE pathway [J]. Annu Rev Pharmacol Toxicol, 2007, 47:89-116.
[11] Cui J, Liu J, Wu S,et al.Oxidative DNA damage is involved in ochratoxin A-induced G2arrest through ataxia telangiectasia-mutated (ATM) pathwaysin human gastric epithelium GES-1 cells in vitro [J]. Arch Toxicol,2013, 87(10):1829-1840.
[12] Somy Yoon, Wei Tao Cong, Yeojin Bang, et al. Proteome response to ochratoxin A-induced apoptotic cell death in mousehippocampal HT22 cells [J]. Mutagenesis, 2007, 22(1): 35-42.
[13] Robbiano L, Baroni D, Carrozzino R, et al. DNA damage and micronuclei induced in rat and humankidney cells by six chemicals carcinogenic to the rat kidney [J]. Toxicology, 2004, 204(2-3): 187-195.
[14] Liu J, Wu S, Shen H, et al. OchratoxinAinduces DNA damage and G2 phase arrest in human esophageal epithelium Het-1A cells in vitro [J].J Toxicol Sci, 2015, 40(5):657-665.
[15] Liu J, Wang Y, Cui J, et al.Ochratoxin A induces oxidative DNA damage and G1 phase arrest in humanperipheral blood mononuclear cells in vitro [J]. ToxicolLett, 2012, 211(2):164-171.
[16] Kamp H G, Eisenbrandt G, Schlatter J, et al. Ochratoxin A: induction of (oxidative) DNA damage, cytotoxicity and apoptosis in mammalian cell lines and primary cells [J]. Toxicology, 2005, 206(3): 413-425.
[17] Kamp H G, Eisenbrand G, Janzowski C, et al. OchratoxinA induces oxidative DNA damage in liver and kidney afteroral dosing to rats [J]. Molecular Nutrition and Food Research, 2005, 49(12): 1160-1167.
[18] Dalle-Donne I, Rossi R, Colombo R, et al. Biomarkers of oxidative damage in human disease [J]. Clin Chem, 2006, 52(4): 601-623.
[19] Gagliano N, Donne I D, Torri C, et al. Early cytotoxic effects of ochratoxinA in rat liver: a morphological, biochemical and molecular study [J]. Toxicology, 2006, 225 (2-3): 214-224.
[20] Domijan A M, Rudes K, Peraica M.The effect ofochratoxin A on the concentration of protein carbonyls inrats [J].Arh Hig Rada Toksikol, 2005, 56(4):311-315.
[21] Rahimtula A D, Bereziat J C, Bussacchini-Griot V, et al. Lipid peroxidation as a possible cause of ochratoxin A toxicity [J].Biochemical Pharmacology, 1998, 37(23): 4469-4477.
[22] Khan S, Martin M, Bartsch H, et al. Perturbation of liver microsomal calcium homeostasis byochratoxin A [J]. Biochemical Pharmacology, 1989, 38(1): 67-72.
[23] Marin-Kuan M, Nestler S, Verguet C, et al. A toxicogenomics approach to identifynew plausible epigenetic mechanisms of ochratoxinAcarcinogenicityin rat [J].ToxicolSci, 2006, 89(1): 120-134.
[24] Wang Y, Liu J, Cui J,et al. ERK and p38 MAPK signaling pathways are involved in ochratoxin A-induced G2phase arrest in human gastric epithelium cells [J].Toxicol Lett,2012,Mar 7,209(2):186-192.
[25] Kumar R L, Ansari K M, Chaudhari B P, et al.Topical application of ochratoxin A causes DNA damage and tumor initiation in mouse skin [J]. Plos One. 2012; 7(10): e47280.
[26] Marin-Kuan M, Nestler S, Verguet C. MAPK-ERK activation in kidney of male rats chronically fed ochratoxin A at a dosecausing a signi cant incidence of renal carcinoma [J]. ToxicolApplPharmacol, 2007, 224(2): 174-181.
[27] Rached E, Hard G C, Blumbach K, et al. Ochratoxin A: 13-week oral toxicity and cell proliferation in male F344/n rats [J]. ToxicolSci, 2007, 97(2): 288-298.
[28] Tsurusaki Y, Yamaguchi M. Role of regucalcin in liver nuclearfunction: binding of regucalcin to nuclear protein or DNA andmodulation of tumor-related gene expression [J]. Int J Mol Med,2004,14(2):277-281.
[29] Stemmer K, Ellinger-Ziegelbauer H, Ahr HJ, et al. Carcinogen-specific gene expression profiles in short-term treated Ekerandwild-type rats indicative of pathways involved in renal tumorigenesis[J]. Cancer Res, 2007, 67(9): 4052-4068.

基金

国家自然科学基金面上项目(基金代码 81171889)

PDF(599 KB)

Accesses

Citation

Detail

段落导航
相关文章

/