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Dickkopf homolog 3 (DKK3): A candidate for detection and treatment of cancers?
Hamzehzadeh, Leila; Caraglia, Michele; Atkin, Stephen L; Sahebkar, Amirhossein.
Afiliação
  • Hamzehzadeh L; Department of Medical Genetics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Caraglia M; Department of Biochemistry, Biophysics and General Pathology, University of Campania "L. Vanvitelli", Naples, Italy.
  • Atkin SL; Weill Cornell Medicine Qatar, Doha, Qatar.
  • Sahebkar A; Biotechnology Research Center, Mashhad University of Medical Sciences, Pharmaceutical Technology Institute, Mashhad, Iran.
J Cell Physiol ; 233(6): 4595-4605, 2018 06.
Article em En | MEDLINE | ID: mdl-29206297
ABSTRACT
Wnt signaling is an evolutionary highly conserved pathway that is modulated by several inhibitors and activators, and plays a key role in numerous physiological processes. One of the extracellular Wnt inhibitors is the DKK (Dickkopf Homolog) family which has four members (Dkk1-4) and a unique Dkk3-related gene, Dkkl1 (soggy). DKK3 is a divergent member of the DKK protein family. Evidence suggests that DKK3 may serve as a potential therapeutic target in several types of human cancers. We review here the biological role of DKK3 as a tumor suppressor gene (TSG) or oncogene, and its correlation with various miRNAs. In addition, we discuss the role of polymorphisms and promoter methylation of the DKK3 gene, and of its expression in regulating cancer cell proliferation. Finally, we propose that DKK3 may be considered as both a biomarker and a therapeutic target in different cancers.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Biomarcadores Tumorais / Peptídeos e Proteínas de Sinalização Intercelular / Proliferação de Células / Neoplasias Tipo de estudo: Diagnostic_studies Limite: Animals / Humans Idioma: En Revista: J Cell Physiol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Irã

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Biomarcadores Tumorais / Peptídeos e Proteínas de Sinalização Intercelular / Proliferação de Células / Neoplasias Tipo de estudo: Diagnostic_studies Limite: Animals / Humans Idioma: En Revista: J Cell Physiol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Irã