Dopamine Receptors in Cancer: Are They Valid Therapeutic Targets?

The dopamine receptors (DRs) family includes 5 members with differences in signal transduction and ligand affinity. Abnormal DRs expression has been correlated multiple tumors with their clinical outcome. Thus, it has been proposed that DRs-targeting drugs—developed for other diseases as schizophren...

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Main Authors: Arely Rosas-Cruz BSc, Nohemí Salinas-Jazmín PhD, Marco A. Velasco- Velázquez PhD
Format: Article
Language:English
Published: SAGE Publishing 2021-07-01
Series:Technology in Cancer Research & Treatment
Online Access:https://doi.org/10.1177/15330338211027913
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spelling doaj-513799f933354cefaa628f725cc88a0e2021-07-02T22:03:27ZengSAGE PublishingTechnology in Cancer Research & Treatment1533-03382021-07-012010.1177/15330338211027913Dopamine Receptors in Cancer: Are They Valid Therapeutic Targets?Arely Rosas-Cruz BSc0Nohemí Salinas-Jazmín PhD1Marco A. Velasco- Velázquez PhD2 Posgrado en Ciencias Bioquímicas, UNAM, México Departamento de Farmacología, Facultad de Medicina, Universidad Nacional Autónoma de México (UNAM), México Unidad Periférica de Investigación en Biomedicina Traslacional, Centro Médico Nacional 20 de noviembre ISSSTE / Facultad de Medicina, UNAM, MéxicoThe dopamine receptors (DRs) family includes 5 members with differences in signal transduction and ligand affinity. Abnormal DRs expression has been correlated multiple tumors with their clinical outcome. Thus, it has been proposed that DRs-targeting drugs—developed for other diseases as schizophrenia or Parkinson’s disease—could be helpful in managing neoplastic diseases. In this review, we discuss the role of DRs and the effects of DRs-targeting in tumor progression and cancer cell biology using multiple high-prevalence neoplasms as examples. The evidence shows that DRs are valid therapeutic targets for certain receptor/disease combinations, but the data are inconclusive or contradictory for others. In either case, further studies are required to define the precise role of DRs in tumor progression and propose better therapeutic strategies for their targeting.https://doi.org/10.1177/15330338211027913
collection DOAJ
language English
format Article
sources DOAJ
author Arely Rosas-Cruz BSc
Nohemí Salinas-Jazmín PhD
Marco A. Velasco- Velázquez PhD
spellingShingle Arely Rosas-Cruz BSc
Nohemí Salinas-Jazmín PhD
Marco A. Velasco- Velázquez PhD
Dopamine Receptors in Cancer: Are They Valid Therapeutic Targets?
Technology in Cancer Research & Treatment
author_facet Arely Rosas-Cruz BSc
Nohemí Salinas-Jazmín PhD
Marco A. Velasco- Velázquez PhD
author_sort Arely Rosas-Cruz BSc
title Dopamine Receptors in Cancer: Are They Valid Therapeutic Targets?
title_short Dopamine Receptors in Cancer: Are They Valid Therapeutic Targets?
title_full Dopamine Receptors in Cancer: Are They Valid Therapeutic Targets?
title_fullStr Dopamine Receptors in Cancer: Are They Valid Therapeutic Targets?
title_full_unstemmed Dopamine Receptors in Cancer: Are They Valid Therapeutic Targets?
title_sort dopamine receptors in cancer: are they valid therapeutic targets?
publisher SAGE Publishing
series Technology in Cancer Research & Treatment
issn 1533-0338
publishDate 2021-07-01
description The dopamine receptors (DRs) family includes 5 members with differences in signal transduction and ligand affinity. Abnormal DRs expression has been correlated multiple tumors with their clinical outcome. Thus, it has been proposed that DRs-targeting drugs—developed for other diseases as schizophrenia or Parkinson’s disease—could be helpful in managing neoplastic diseases. In this review, we discuss the role of DRs and the effects of DRs-targeting in tumor progression and cancer cell biology using multiple high-prevalence neoplasms as examples. The evidence shows that DRs are valid therapeutic targets for certain receptor/disease combinations, but the data are inconclusive or contradictory for others. In either case, further studies are required to define the precise role of DRs in tumor progression and propose better therapeutic strategies for their targeting.
url https://doi.org/10.1177/15330338211027913
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