Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/75088
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Type: Conference paper
Title: Using X-ray absorption spectroscopy and microprobe synchrotron radiation-X-ray fluorescence imaging for understanding the mode of action of arsenic anti-leukaemia agents
Author: Munro, K.
Dillon, C.
Harris, H.
Cai, Z.
Lai, B.
Vogt, S.
Cheah, M.
Citation: Understanding the Geological and Medical Interface of Arsenic - AS 2012: Proceedings of the 4th International Congress on Arsenic in the Environment, 22-27 July 2012, Cairns, Australia / J.C. Ng, B.N. Noller, R. Naidu (eds.): pp.193-195
Publisher: CRC Press
Publisher Place: UK
Issue Date: 2012
Series/Report no.: Arsenic in the Environment
ISBN: 9780415637633
ISSN: 1876-6218
Conference Name: International Congress on Arsenic in the Environment (4th : 2012 : Cairns, Qld.)
Editor: Ng, J.C.
Noller, B.N.
Naidu, R.
Bundschuh, J.
Bhattacharya, P.
Statement of
Responsibility: 
K.L. Munro, C.T. Dillon, H.H. Harris, Z. Cai, B. Lai, S. Vogt & M. Cheah
Abstract: Despite its reputation as a poison, arsenic is also a highly effective anti-leukaemia agent. In order to improve on its efficacy, a better understanding of the metabolism of arsenic, including the formation of specific arsenic metabolites, is necessary. In this study XAS was used to gain an understanding of the metabolism of arsenic in human hepatoma cells and microprobe SR-XRF imaging was used to determine potential targets for the identified arsenic species. It was found that the toxic arsenic metabolites, [MMAIII(GS)2] and [DMAIII(GS)], were produced in human cells and that these metabolites potentially interact with DNA or, more probably, proteins associated with DNA transcription. © 2012 Taylor & Francis Group.
Rights: Copyright status unknown
DOI: 10.1201/b12522-76
Appears in Collections:Aurora harvest
Environment Institute publications
IPAS publications

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