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Glutathione Transferases: Potential Targets to Overcome Chemoresistance in Solid Tumors.
Pljesa-Ercegovac, Marija; Savic-Radojevic, Ana; Matic, Marija; Coric, Vesna; Djukic, Tatjana; Radic, Tanja; Simic, Tatjana.
Afiliação
  • Pljesa-Ercegovac M; Institute of Medical and Clinical Biochemistry, Faculty of Medicine, University of Belgrade, 11 000 Belgrade, Serbia. m.pljesa.ercegovac@gmail.com.
  • Savic-Radojevic A; Faculty of Medicine, University of Belgrade, 11 000 Belgrade, Serbia. m.pljesa.ercegovac@gmail.com.
  • Matic M; Institute of Medical and Clinical Biochemistry, Faculty of Medicine, University of Belgrade, 11 000 Belgrade, Serbia. ana.savic-radojevic@med.bg.ac.rs.
  • Coric V; Faculty of Medicine, University of Belgrade, 11 000 Belgrade, Serbia. ana.savic-radojevic@med.bg.ac.rs.
  • Djukic T; Institute of Medical and Clinical Biochemistry, Faculty of Medicine, University of Belgrade, 11 000 Belgrade, Serbia. marija_opacic@yahoo.com.
  • Radic T; Faculty of Medicine, University of Belgrade, 11 000 Belgrade, Serbia. marija_opacic@yahoo.com.
  • Simic T; Institute of Medical and Clinical Biochemistry, Faculty of Medicine, University of Belgrade, 11 000 Belgrade, Serbia. coricmvesna@gmail.com.
Int J Mol Sci ; 19(12)2018 Nov 28.
Article em En | MEDLINE | ID: mdl-30487385
Multifunctional enzymes glutathione transferases (GSTs) are involved in the development of chemoresistance, thus representing a promising target for a novel approach in cancer treatment. This superfamily of polymorphic enzymes exhibits extraordinary substrate promiscuity responsible for detoxification of numerous conventional chemotherapeutics, at the same time regulating signaling pathways involved in cell proliferation and apoptosis. In addition to upregulated GST expression, different cancer cell types have a unique GST signature, enabling targeted selectivity for isoenzyme specific inhibitors and pro-drugs. As a result of extensive research, certain GST inhibitors are already tested in clinical trials. Catalytic properties of GST isoenzymes are also exploited in bio-activation of specific pro-drugs, enabling their targeted accumulation in cancer cells with upregulated expression of the appropriate GST isoenzyme. Moreover, the latest approach to increase specificity in treatment of solid tumors is development of GST pro-drugs that are derivatives of conventional anti-cancer drugs. A future perspective is based on the design of new drugs, which would selectively target GST overexpressing cancers more prone to developing chemoresistance, while decreasing side effects in off-target cells.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Inibidores Enzimáticos / Glutationa Transferase Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Inibidores Enzimáticos / Glutationa Transferase Idioma: En Ano de publicação: 2018 Tipo de documento: Article