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Targeting dopamine pathways with hybrid molecules: Emerging outlook for cancer treatment.

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European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V 2026 Vol.222() p. 115031 Cancer, Stress, Anesthesia, and Immu
TL;DR This review synthesizes current advances in DA-pathway-targeting hybrid constructs, explores their mechanistic rationale, and highlights the major biological and translational challenges that must be addressed to support their development.
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PubMed DOI OpenAlex Semantic 마지막 보강 2026-04-29
OpenAlex 토픽 · Cancer, Stress, Anesthesia, and Immune Response Nerve injury and regeneration Neuropeptides and Animal Physiology

Koch P, Pielaszkiewicz N, Małek K, Kamysz W, Kleczkowska P

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This review synthesizes current advances in DA-pathway-targeting hybrid constructs, explores their mechanistic rationale, and highlights the major biological and translational challenges that must be

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APA Piotr Koch, Natalia Pielaszkiewicz, et al. (2026). Targeting dopamine pathways with hybrid molecules: Emerging outlook for cancer treatment.. European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 222, 115031. https://doi.org/10.1016/j.ejpb.2026.115031
MLA Piotr Koch, et al.. "Targeting dopamine pathways with hybrid molecules: Emerging outlook for cancer treatment.." European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, vol. 222, 2026, pp. 115031.
PMID 41724450 ↗

Abstract

Dopamine (DA)-related signaling has increasingly been recognized as a contributor to cellular regulation, affecting pathways associated with growth, survival, and receptor-mediated signaling. This understanding has motivated the development of hybrid therapeutic platforms that combine dopaminergic modulation with additional strategies, such as receptor co-targeting and selective drug delivery. These systems encompass diverse molecular formats, including multifunctional peptide chimeras acting on dopaminergic and somatostatin receptors, as well as DA-functionalized nanomaterials or polymeric conjugates. Collectively, these hybrids demonstrate the potential for enhanced pharmacologic precision, improved intracellular accumulation, and reduced off-target effects as compared to those of conventional compounds. Despite promising preclinical evidence, multiple barriers remain before these technologies can be translated clinically. This review synthesizes current advances in DA-pathway-targeting hybrid constructs, explores their mechanistic rationale, and highlights the major biological and translational challenges that must be addressed to support their development.

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