Peptidergic Systems and Neuroblastoma
Manuel Lisardo Sánchez, Rafael Coveñas

TL;DR
Peptidergic systems play a complex role in neuroblastoma, with some peptides promoting cancer and others inhibiting it, offering potential for new treatments.
Contribution
The paper highlights the dual role of peptidergic systems in neuroblastoma and their potential as therapeutic targets.
Findings
Oncogenic peptides like angiotensin II and neuropeptide Y promote neuroblastoma progression.
Anticancer peptides such as adrenomedullin and orexin inhibit neuroblastoma cell growth and angiogenesis.
Peptide receptor antagonists and other therapeutic approaches show promise in counteracting oncogenic effects.
Abstract
The peptidergic systems are involved in neuroblastoma. Peptides (angiotensin II, neuropeptide Y, neurotensin, substance P) act as oncogenic agents in neuroblastoma, whereas others (adrenomedullin, corticotropin-releasing factor, urocortin, orexin) exert anticancer effects against neuroblastoma. This plethora of peptidergic systems show the functional complexity of the mechanisms regulated by peptides in neuroblastoma. Peptide receptor antagonists act as antineuroblastoma agents since these compounds counteracted neuroblastoma cell growth and migration and the angiogenesis promoted by oncogenic peptides. Other therapeutic approaches (signaling pathway inhibitors, focal adhesion kinase inhibitors, peptide receptor knockdown, acetic acid analogs) that also counteract the beneficial effects mediated by the oncogenic peptides in neuroblastoma are discussed, and future research lines to be…
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Taxonomy
TopicsNeuroblastoma Research and Treatments · Neuropeptides and Animal Physiology · Neuroendocrine Tumor Research Advances
