Publication: Neurokinin-1 Receptor (NK-1R) Antagonists as a New Strategy to Overcome Cancer Resistance.
Identifiers
Date
2022-04-30
Authors
Garcia-Aranda, Marilina
Tellez, Teresa
McKenna, Lauraine
Redondo, Maximino
Advisors
Journal Title
Journal ISSN
Volume Title
Publisher
MDPI AG
Abstract
Nowadays, the identification of new therapeutic targets that allow for the development of treatments, which as monotherapy, or in combination with other existing treatments can contribute to improve response rates, prognosis and survival of oncologic patients, is a priority to optimize healthcare within sustainable health systems. Recent studies have demonstrated the role of Substance P (SP) and its preferred receptor, Neurokinin 1 Receptor (NK-1R), in human cancer and the potential antitumor activity of NK-1R antagonists as an anticancer treatment. In this review, we outline the relevant studies published to date regarding the SP/NK-1R complex as a key player in human cancer and also evaluate if the repurposing of already marketed NK-1R antagonists may be useful in the development of new treatment strategies to overcome cancer resistance.
Description
MeSH Terms
Substance P
Receptors, Neurokinin-1
Neoplasms
Drug Resistance, Neoplasm
Therapeutic Equivalency as Topic
Antineoplastic Agents, Targeted
Receptors, Neurokinin-1
Neoplasms
Drug Resistance, Neoplasm
Therapeutic Equivalency as Topic
Antineoplastic Agents, Targeted
DeCS Terms
Sustancia P
Receptores de Neuroquinina-1
Neoplasias
Antagonistas de receptores de Neuroquinina-1
Uso terapéutico de fármacos
Resistencia a fármacos
Medicina personalizada
Cáncer
Receptores de Neuroquinina-1
Neoplasias
Antagonistas de receptores de Neuroquinina-1
Uso terapéutico de fármacos
Resistencia a fármacos
Medicina personalizada
Cáncer
CIE Terms
Keywords
NK-1R, cancer, drug repurposing, personalized medicine, resistance, tachykinin, tachykinin receptor, targeted treatment
Citation
García-Aranda M, Téllez T, McKenna L, Redondo M. Neurokinin-1 Receptor (NK-1R) Antagonists as a New Strategy to Overcome Cancer Resistance. Cancers (Basel). 2022 Apr 30;14(9):2255