Dopamine and serotonin regulate tumor behavior by affecting angiogenesis

Marloes Peters, Annemiek M. E. Walenkamp, Ido P. Kema, Coby Meijer, Elisabeth G. E. de Vries, Sjoukje F. Oosting*

*Corresponding author for this work

    Research output: Contribution to journalReview articlepeer-review

    61 Citations (Scopus)

    Abstract

    The biogenic amines dopamine and serotonin are neurotransmitters and hormones, which are mainly produced in the central nervous system and in the gastro-intestinal tract. They execute local and systemic functions such as intestinal motility and tissue repair. Dopamine and serotonin are primarily stored in and transported by platelets. This review focuses on the recently recognized role of dopamine and serotonin in the regulation of tumor behavior by affecting angiogenesis and tumor cell proliferation. Preclinical studies demonstrate that dopamine inhibits tumor growth via activation of dopamine receptor D2 on endothelial and tumor cells. Serotonin stimulates tumor growth via activation of serotonin receptor 2B on endothelial cells and serotonin receptors on tumor cells. Drugs that stimulate dopamine receptor D2 or inhibit serotonin receptors are available and therefore clinical intervention studies for cancer patients are within reach. (C) 2014 Elsevier Ltd. All rights reserved.

    Original languageEnglish
    Pages (from-to)96-104
    Number of pages9
    JournalDrug Resistance Updates
    Volume17
    Issue number4-6
    DOIs
    Publication statusPublished - 2014

    Keywords

    • Dopamine
    • Serotonin
    • Biogenic amines
    • Angiogenesis
    • Cancer
    • ENDOTHELIAL GROWTH-FACTOR
    • OVARIAN HYPERSTIMULATION SYNDROME
    • CANCER CELL-PROLIFERATION
    • NITRIC-OXIDE SYNTHASE
    • HUMAN BREAST-CANCER
    • PARKINSONS-DISEASE
    • BLOOD-PLATELETS
    • LUNG-CANCER
    • BONE-MARROW
    • MOUSE MODEL

    Fingerprint

    Dive into the research topics of 'Dopamine and serotonin regulate tumor behavior by affecting angiogenesis'. Together they form a unique fingerprint.

    Cite this