Eco-genotoxicity of six anticancer drugs using comet assay in daphnids

被引:67
作者
Parrella, Alfredo [1 ]
Lavorgna, Margherita [1 ]
Criscuolo, Emma [1 ]
Russo, Chiara [1 ]
Isidori, Marina [1 ]
机构
[1] Univ Naples 2, Dipartimento Sci & Tecnol Ambientali, Biol & Farmaceut, I-81100 Caserta, Italy
关键词
Anticancer drugs; Genotoxicity; Daphnia magna; Ceriodaphnia dubia; Mutagenicity; DNA-DAMAGE; IN-VITRO; WASTE-WATER; IMATINIB; METABOLITES; SURFACE; VIVO;
D O I
10.1016/j.jhazmat.2015.01.012
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The eco-genotoxicity of six anti-neoplastic drugs, 5-fluorouracil, capecitabine, cisplatin, doxorubicin, etoposide, and imatinib, belonging to five classes of anatomical therapeutic classification (ATC), was studied applying the in vivo comet assay on cells from whole organisms of Daphnia magna and Ceriodaphnia dubia. For the first time, this test was performed in C. dubia. In addition, to have a wider genotoxic/mutagenic profile of the anticancer drugs selected, SOS chromotest and Salmonella mutagenicity assay were performed. The comet results showed that all drugs induced DNA damage, in both Cladocerans, with environmental concern; indeed Doxorubicin induced DNA damage in the order of tens of ng L-1 in both crustaceans, as well as 5-flurouracil in C dubia and cisplatin in D. magna. In the SOS Chromotest all drugs, except imatinib, were able to activate the repair system in Escherichia coil PQ37 while in the Salmonella mutagenicity assay, doxorubicin was the only drug able to cause direct and indirect frameshift and base-pair substitution mutations. Comet assay was the most sensitive tool of genotoxic exposure assessment, able to detect in vivo the adverse effects at concentration lower than those evaluated in vitro by bacterial assays. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:573 / 580
页数:8
相关论文
共 35 条
[1]  
[Anonymous], 1983, EPA600482068
[2]  
[Anonymous], 2008, 20665 ISO
[3]  
[Anonymous], 2000, Water quality - determination of the genotoxicity of water and waste water using the umu-test (ISO 13829)
[4]  
[Anonymous], 2003, NOV MAT SAF DAT SHEE
[5]   Anticancer drugs in surface waters What can we say about the occurrence and environmental significance of cytotoxic, cytostatic and endocrine therapy drugs? [J].
Besse, Jean-Philippe ;
Latour, Jean-Francois ;
Garric, Jeanne .
ENVIRONMENT INTERNATIONAL, 2012, 39 (01) :73-86
[6]   Toxicities of four anti-neoplastic drugs and their binary mixtures tested on the green alga Pseudokirchneriella subcapitata and the cyanobacterium Synechococcus leopoliensis [J].
Brezovsek, Polona ;
Elersek, Tina ;
Filipic, Metka .
WATER RESEARCH, 2014, 52 :168-177
[7]   Transcriptional responses in neonate and adult Daphnia magna in relation to relative susceptibility to genotoxicants [J].
David, Rhiannon M. ;
Dakic, Vanja ;
Williams, Timothy D. ;
Winter, Matthew J. ;
Chipman, J. Kevin .
AQUATIC TOXICOLOGY, 2011, 104 (3-4) :192-204
[8]   Effects of the novel DNA dependent protein kinase inhibitor, IC486241, on the DNA damage response to doxorubicin and cisplatin in breast cancer cells [J].
Davidson, David ;
Grenier, Jeremy ;
Martinez-Marignac, Veronica ;
Amrein, Lilian ;
Shawi, May ;
Tokars, Marc ;
Aloyz, Raquel ;
Panasci, Lawrence .
INVESTIGATIONAL NEW DRUGS, 2012, 30 (04) :1736-1742
[9]   Centrosome aberrations after nilotinib and imatinib treatment in vitro are associated with mitotic spindle defects and genetic instability [J].
Fabarius, Alice ;
Giehl, Michelle ;
Frank, Oliver ;
Spiess, Birgit ;
Zheng, Chun ;
Mueller, Martin C. ;
Weiss, Christel ;
Duesberg, Peter ;
Hehlmann, Ruediger ;
Hochhaus, Andreas ;
Seifarth, Wolfgang .
BRITISH JOURNAL OF HAEMATOLOGY, 2007, 138 (03) :369-373
[10]   Genotoxic effects of wastewater from an oncological ward [J].
Ferk, Franziska ;
Misik, Miroslav ;
Grummt, Tamara ;
Majer, Bernhard ;
Fuerhacker, Maria ;
Buchmann, Christoph ;
Vital, Marius ;
Uhl, Maria ;
Lenz, Katharina ;
Grillitsch, Britta ;
Parzefall, Wolfram ;
Nersesyan, Armen ;
Knasmueller, Siegfried .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2009, 672 (02) :69-75