In vitro Cytotoxicity and Genotoxicity Analysis of Ten Tannery Chemicals Using SOS/umu Tests and High-content in vitro Micronucleus Tests

被引:2
作者
Huang, Zehao [1 ,2 ]
Li, Na [3 ]
Rao, Kaifeng [3 ]
Liu, Cuiting [4 ]
Wang, Zijian [2 ]
Ma, Mei [5 ,6 ]
机构
[1] Univ Chinese Acad Sci, Beijing, Peoples R China
[2] Chinese Acad Sci, Res Ctr Ecoenvironm Sci, State Key Lab Environm Aquat Chem, Beijing, Peoples R China
[3] Chinese Acad Sci, Res Ctr Ecoenvironm Sci, Beijing, Peoples R China
[4] Guangzhou Med Univ, Affiliated Hosp 3, Guangzhou, Guangdong, Peoples R China
[5] Chinese Acad Sci, Res Ctr Ecoenvironm, Key Lab Drinking Water Sci & Technol, Beijing, Peoples R China
[6] Univ Chinese Acad Sci, Coll Resources & Environm, Beijing, Peoples R China
关键词
SOS/umu tests; high-content screening; in vitro micronucleus tests; cytotoxicity; genotoxicity; tannery chemicals; UMU-TEST; ASSAY; CARCINOGENICITY; VALIDATION; METABOLISM; ACTIVATION; CELLS; HEPG2; VIVO;
D O I
10.2174/1386207321666180330120248
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: More than 2,000 chemicals have been used in the tannery industry. Although some tannery chemicals have been reported to have harmful effects on both human health and the environment, only a few have been subjected to genotoxicity and cytotoxicity evaluations. Objective: This study focused on cytotoxicity and genotoxicity of ten tannery chemicals widely used in China. Materials and Methods: DNA-damaging effects were measured using the SOS/umu test with Salmonella typhimurium TA1535/pSK1002. Chromosome-damaging and cytotoxic effects were determined with the high-content in vitro Micronucleus test (MN test) using the human-derived cell lines MGC-803 and A549. Conclusion: The cytotoxicity of the ten tannery chemicals differed somewhat between the two cell assays, with A549 cells being more sensitive than MGC-803 cells. None of the chemicals induced DNA damage before metabolism, but one was found to have DNA-damaging effects on metabolism. Four of the chemicals, DY64, SB1, DB71 and RR120, were found to have chromosome-damaging effects. A Quantitative Structure-Activity Relationship (QSAR) analysis indicated that one structural feature favouring chemical genotoxicity, Hacceptor-path3-Hacceptor, may contribute to the chromosome-damaging effects of the four MN-test-positive chemicals.
引用
收藏
页码:262 / 270
页数:9
相关论文
共 27 条
  • [1] [Anonymous], 2000, GUID STRAT TEST CHEM
  • [2] Scientific opinion on genotoxicity testing strategies applicable to food and feed safety assessment
    Antunovic, Boris
    Barlow, Susan
    Chesson, Andrew
    Flynn, Albert
    Hardy, Anthony
    Jeger, Michael-John
    Knaap, Ada
    Kuiper, Harry
    Larsen, John-Christian
    Lovell, David
    Noerrung, Birgit
    Pratt, Iona
    Rietjens, Ivonne
    Schlatter, Josef
    Silano, Vittorio
    Smulders, Frans
    Vannier, Philippe
    [J]. EFSA JOURNAL, 2011, 9 (09)
  • [3] WORKSHOP ON THE RELATIONSHIP BETWEEN SHORT-TERM TEST INFORMATION AND CARCINOGENICITY, WILLIAMSBURG, VIRGINIA, JANUARY 20-23, 1987
    AULETTA, A
    ASHBY, J
    [J]. ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 1988, 11 (01) : 135 - 145
  • [4] In vivo experiments for the evaluation of genotoxic and cytotoxic effects of Triclosan in Zebra mussel hemocytes
    Binelli, A.
    Cogni, D.
    Parolini, M.
    Riva, C.
    Provini, A.
    [J]. AQUATIC TOXICOLOGY, 2009, 91 (03) : 238 - 244
  • [5] The applicability of in vitro-derived data in hazard identification and characterisation of chemicals
    Blaauboer, BJ
    [J]. ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY, 2002, 11 (3-4) : 213 - 225
  • [6] Metabolism and bioactivation of toxicants in the lung.: The in vitro cellular approach
    Castell, JV
    Donato, MT
    Gómez-Lechón, MJ
    [J]. EXPERIMENTAL AND TOXICOLOGIC PATHOLOGY, 2005, 57 : 189 - 204
  • [7] ICH S2(R1), 2011, GUID GEN TEST DAT IN, P1
  • [8] Active Wnt signalling is associated with low differentiation and high proliferation in human biliary tract cancer in vitro and in vivo and is sensitive to pharmacological inhibition
    Kiesslich, Tobias
    Alinger, Beate
    Wolkersdoerfer, Gernot W.
    Ocker, Matthias
    Neureiter, Daniel
    Berr, Frieder
    [J]. INTERNATIONAL JOURNAL OF ONCOLOGY, 2010, 36 (01) : 49 - 58
  • [9] Report from the in vitro micronucleus assay working group
    Kirsch-Volders, M
    Sofuni, T
    Aardema, C
    Albertini, S
    Eastmond, D
    Fenech, M
    Ishidate, M
    Kirchner, S
    Lorge, E
    Morita, T
    Norppa, H
    Surrallés, J
    Vanhauwaert, A
    Wakata, A
    [J]. MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2003, 540 (02) : 153 - 163
  • [10] Hypoxia-inducible factor-1α obstructs a Wnt signaling pathway by inhibiting the hARD1-mediated activation of β-catenin
    Lim, Ji-Hong
    Chun, Yang-Sook
    Park, Jong-Wan
    [J]. CANCER RESEARCH, 2008, 68 (13) : 5177 - 5184