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Proteoglycans-Biomarkers and Targets in Cancer Therapy.
Nikitovic, Dragana; Berdiaki, Aikaterini; Spyridaki, Ioanna; Krasanakis, Theodoros; Tsatsakis, Aristidis; Tzanakakis, George N.
Afiliação
  • Nikitovic D; Laboratory of Anatomy-Histology-Embryology, Medical School, University of Crete, Heraklion, Greece.
  • Berdiaki A; Laboratory of Anatomy-Histology-Embryology, Medical School, University of Crete, Heraklion, Greece.
  • Spyridaki I; Laboratory of Anatomy-Histology-Embryology, Medical School, University of Crete, Heraklion, Greece.
  • Krasanakis T; Laboratory of Anatomy-Histology-Embryology, Medical School, University of Crete, Heraklion, Greece.
  • Tsatsakis A; Laboratory of Toxicology, Medical School, University of Crete, Heraklion, Greece.
  • Tzanakakis GN; Laboratory of Anatomy-Histology-Embryology, Medical School, University of Crete, Heraklion, Greece.
Article em En | MEDLINE | ID: mdl-29559954
ABSTRACT
Proteoglycans (PGs), important constituents of the extracellular matrix, have been associated with cancer pathogenesis. Their unique structure consisting of a protein core and glycosaminoglycan chains endowed with fine modifications constitutes these molecules as capable cellular effectors important for homeostasis and contributing to disease progression. Indeed, differential expression of PGs and their interacting proteins has been characterized as specific for disease evolvement in various cancer types. Importantly, PGs to a large extent regulate the bioavailability of hormones, growth factors, and cytokines as well as the activation of their respective receptors which regulate phenotypic diversibility, gene expression and rates of recurrence in specific tumor types. Defining and targeting these effectors on an individual patient basis offers ground for the development of newer therapeutic approaches which may act as either supportive or a substitute treatment to the standard therapy protocols. This review discusses the roles of PGs in cancer progression, developing technologies utilized for the defining of the PG "signature" in disease, and how this may facilitate the generation of tailor-made cancer strategies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Revista: Front Endocrinol (Lausanne) Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Grécia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Revista: Front Endocrinol (Lausanne) Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Grécia