Web of Science: 2 citations, Scopus: 2 citations, Google Scholar: citations
Formation of cyclobutane thymine dimers by tiaprofenic acid and its photoproducts : approach to the photosensitizer triplet state energy limit value
Michaud, Sandra (Université Paul Sabatier)
Bordeau, Guillaume (Université Paul Sabatier)
Sartor, Valérie (Université Paul Sabatier)
Bourdelande, J. L. (José Luis) (Universitat Autònoma de Barcelona. Departament de Química)
Hernando Campos, Jordi (Universitat Autònoma de Barcelona. Departament de Química)
Guirado López, Gonzalo (Universitat Autònoma de Barcelona. Departament de Química)
Chouini-Lalanne, Nadia (Université Paul Sabatier)

Date: 2015
Abstract: Cyclobutane thymine dimers, the major photoproducts produced in UV-irradiated DNA, are the main causative agents for mutagenesis and skin cancer. This lesion can also be initiated under UVA radiation, involving triplet-triplet energy transfer mechanism from a photosensitizer to the thymine nucleobase. According to previous reports, only photosensitizers with a triplet state energy >270 kJ mol<sup>-1</sup> should be able to induce cyclobutane thymine dimers photosensitization. However, tiaprofenic acid, a non-steroidal anti-inflammatory drug widely prescribed in the treatment of inflammation and pain, has shown cyclobutane thymine dimers photosensitization, although its triplet energy state value and those of its photoproducts are lower than the one previously reported for thymine in DNA. In this context, the in vitro photosensitizing properties of tiaprofenic acid and its photoproducts were studied by agarose gel electrophoresis and phosphorescence experiments and demonstrated clearly the formation of cyclobutane thymine dimers by tiaprofenic acid and its photoproducts. This study allows us to approach the lower limit threshold of the triplet state energy of a photosensitizer for cyclobutane thymine dimers formation and thereby to improve the prediction of the photogenotoxic potential of current and future drugs.
Grants: Ministerio de Economía y Competitividad CTQ2012-30853
Rights: Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original. Creative Commons
Language: Anglès
Document: Article ; recerca ; Versió publicada
Subject: Agarose gel electrophoresis ; Causative agents ; Cyclobutane-thymine dimers ; Non-steroidal anti-inflammatory drugs ; Triplet energy ; Triplet state energies ; Triplet-triplet energy transfer ; UV-A-radiation
Published in: RSC advances, Vol. 5, Issue 84 (2015) , p. 68595-68600, ISSN 2046-2069

DOI: 10.1039/c5ra11869g


6 p, 487.8 KB

The record appears in these collections:
Research literature > UAB research groups literature > Research Centres and Groups (research output) > Experimental sciences > Group in Electrochemistry, Photochemistry and Organic Reactivity (GEFRO)
Articles > Research articles
Articles > Published articles

 Record created 2019-11-26, last modified 2022-02-06



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