TY - JOUR
T1 - Gene-mutation induction by arsenic compounds in the mouse lymphoma assay
AU - Soriano, Carolina
AU - Creus, Amadeu
AU - Marcos, Ricard
N1 - Funding Information:
C. Soriano is supported by a postgraduate fellowship from the Generalitat de Catalunya. We wish to thank Dr. Peter Jenkinson (SafePharm Laboratories, Derby, UK) for his warm reception to C.S. during her stay in his laboratory to learn some technical aspects of the MLA. This investigation has been supported in part by the Spanish Ministry of Education and Science (CAICYT, VEM2004-08597) and the Generalitat de Catalunya (CIRIT, 2005SGR-00136).
PY - 2007/12/1
Y1 - 2007/12/1
N2 - Arsenic compounds are generally considered as poor inducers of gene mutations. To investigate the mutagenicity of several arsenic compounds at the thymidine kinase (Tk) gene, a reporter gene for mutation induction, we used the mouse lymphoma assay (MLA). This test is widely applied and detects a broad spectrum of mutational events, from point mutations to chromosome alterations. The selected arsenic compounds were two inorganic (sodium arsenite and arsenic trioxide) and four organic compounds (monomethylarsonic acid, dimethylarsinic acid, tetraphenylarsenium and arsenobetaine). The results show that sodium arsenite, arsenic trioxide, monomethylarsonic acid and dimethylarsinic acid are mutagenic, showing a clear dose-response pattern. On the other hand, tetraphenylarsenium and arsenobetaine are not mutagenic. Inorganic arsenic compounds are the more potent agents producing significant effects in the micromolar range, while the mutagenic organic arsenic compounds induce similar effects but in the millimolar range.
AB - Arsenic compounds are generally considered as poor inducers of gene mutations. To investigate the mutagenicity of several arsenic compounds at the thymidine kinase (Tk) gene, a reporter gene for mutation induction, we used the mouse lymphoma assay (MLA). This test is widely applied and detects a broad spectrum of mutational events, from point mutations to chromosome alterations. The selected arsenic compounds were two inorganic (sodium arsenite and arsenic trioxide) and four organic compounds (monomethylarsonic acid, dimethylarsinic acid, tetraphenylarsenium and arsenobetaine). The results show that sodium arsenite, arsenic trioxide, monomethylarsonic acid and dimethylarsinic acid are mutagenic, showing a clear dose-response pattern. On the other hand, tetraphenylarsenium and arsenobetaine are not mutagenic. Inorganic arsenic compounds are the more potent agents producing significant effects in the micromolar range, while the mutagenic organic arsenic compounds induce similar effects but in the millimolar range.
KW - Arsenic compounds
KW - Gene-mutation
KW - Mouse lymphoma assay
KW - Mutant frequency
KW - Tk
UR - https://www.scopus.com/pages/publications/35448997211
U2 - 10.1016/j.mrgentox.2007.05.014
DO - 10.1016/j.mrgentox.2007.05.014
M3 - Article
C2 - 17851118
AN - SCOPUS:35448997211
SN - 1383-5718
VL - 634
SP - 40
EP - 50
JO - Mutation Research - Genetic Toxicology and Environmental Mutagenesis
JF - Mutation Research - Genetic Toxicology and Environmental Mutagenesis
IS - 1-2
ER -