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Targeting iron to contrast cancer progression.
Tomat, Elisa.
Afiliação
  • Tomat E; Department of Chemistry and Biochemistry, The University of Arizona, 1306 E. University Blvd., Tucson, AZ 85721-0041, USA. Electronic address: tomat@arizona.edu.
Curr Opin Chem Biol ; 74: 102315, 2023 06.
Article em En | MEDLINE | ID: mdl-37187095
ABSTRACT
An altered metabolism of iron fuels cancer growth, invasion, metastasis, and recurrence. Ongoing research in cancer biology is delineating a complex iron-trafficking program involving both malignant cells and their support network of cancer stem cells, immune cells, and other stromal components in the tumor microenvironment. Iron-binding strategies in anticancer drug discovery are being pursued in clinical trials and in multiple programs at various levels of development. Polypharmacological mechanisms of action, combined with emerging iron-associated biomarkers and companion diagnostics, are poised to offer new therapeutic options. By targeting a fundamental player in cancer progression, iron-binding drug candidates (either alone or in combination therapy) have the potential to impact a broad range of cancer types and to address the major clinical problems of recurrence and resistance to therapy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ferro / Neoplasias Limite: Humans Idioma: En Revista: Curr Opin Chem Biol Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ferro / Neoplasias Limite: Humans Idioma: En Revista: Curr Opin Chem Biol Ano de publicação: 2023 Tipo de documento: Article