Literature DB >> 24337356

Alkoxyamines: a new family of pro-drugs against cancer. Concept for theranostics.

Gérard Audran1, Paul Brémond, Jean-Michel Franconi, Sylvain R A Marque, Philippe Massot, Philippe Mellet, Elodie Parzy, Eric Thiaudière.   

Abstract

Development of anti-cancerous theranostic agents is a vivid field. This article describes a theranostic approach that relies on the triggering of cancer cell death by generation of alkyl radicals at the right place and at the right time using the presence of active proteases in the tumour environment. Alkoxyamines (R(1)R(2)NOR(3)) are labile molecules that homolyze into nitroxides (R(1)R(2)NO˙) and reactive alkyl radicals (R(3)˙). They are used as a source of active alkyl radicals for curing and nitroxides for monitoring by Overhauser-enhanced magnetic resonance imaging (OMRI). Herein, the requirements needed for applying alkoxyamines are described: (i) highly selective activation of the alkoxyamine by specific proteases; (ii) fast homolysis of the alkoxyamine C-ON bond at physiological temperature; (iii) activation of cell death processes through an increase of the local oxidative stress or potential re-activation of the immune system due to short-lived alkyl radicals; and (iv) imaging of the tumor and the drug release by sensing the nitroxide by OMRI.

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Year:  2013        PMID: 24337356     DOI: 10.1039/c3ob42076k

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  5 in total

1.  Trityl-based alkoxyamines as NMP controllers and spin-labels.

Authors:  Gérard Audran; Elena G Bagryanskaya; Paul Brémond; Mariya V Edeleva; Sylvain R A Marque; Dmitriy A Parkhomenko; Olga Yu Rogozhnikova; Victor M Tormyshev; Evgeny V Tretyakov; Dmitry V Trukhin; Svetlana I Zhivetyeva
Journal:  Polym Chem       Date:  2016-10-12       Impact factor: 5.582

2.  Photochemical generation of the 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) radical from caged nitroxides by near-infrared two-photon irradiation and its cytocidal effect on lung cancer cells.

Authors:  Ayato Yamada; Manabu Abe; Yoshinobu Nishimura; Shoji Ishizaka; Masashi Namba; Taku Nakashima; Kiyofumi Shimoji; Noboru Hattori
Journal:  Beilstein J Org Chem       Date:  2019-04-10       Impact factor: 2.883

3.  NMR and EPR Study of Homolysis of Diastereomeric Alkoxyamines.

Authors:  Sergey Cherkasov; Dmitriy Parkhomenko; Alexander Genaev; Georgii Salnikov; Mariya Edeleva; Denis Morozov; Tatyana Rybalova; Igor Kirilyuk; Sylvain R A Marque; Elena Bagryanskaya
Journal:  Molecules       Date:  2020-11-01       Impact factor: 4.411

4.  How intramolecular coordination bonding (ICB) controls the homolysis of the C-ON bond in alkoxyamines.

Authors:  Gérard Audran; Elena Bagryanskaya; Irina Bagryanskaya; Mariya Edeleva; Jean-Patrick Joly; Sylvain R A Marque; Anna Iurchenkova; Polina Kaletina; Sergey Cherkasov; Tung To Hai; Evgeny Tretyakov; Svetlana Zhivetyeva
Journal:  RSC Adv       Date:  2019-08-16       Impact factor: 3.361

5.  Neutrophil Elastase-Activatable Prodrugs Based on an Alkoxyamine Platform to Deliver Alkyl Radicals Cytotoxic to Tumor Cells.

Authors:  Seda Seren; Jean-Patrick Joly; Pierre Voisin; Véronique Bouchaud; Gérard Audran; Sylvain R A Marque; Philippe Mellet
Journal:  J Med Chem       Date:  2022-06-28       Impact factor: 8.039

  5 in total

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