Evidence map›Paper›PMID 25963269›Full record

ReviewJournal of biosciences2015

The substance P/NK-1 receptor system: NK-1 receptor antagonists as anti-cancer drugs.

Miguel Munoz, Rafael Covenas, Francisco Esteban, Maximino Redondo

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of biosciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
2.7field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

57 citing papers in PubMed, 100 citations in OpenAlex.

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  16. Substance P-Friend or Foe.Journal of clinical medicine · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 1 country.

Miguel MunozResearch Laboratory on Neuropeptides, Virgen del Rocio University Hospital, Sevilla, Spain, mmunoz@cica.es.
Rafael Covenas
Francisco Esteban
Maximino Redondo
Hospital Universitario Virgen del Rocío · ESHospital Costa del Sol · ESInstituto de Estudios de Ciencias de la Salud de Castilla y León · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The substance P (SP)/neurokinin (NK)-1 receptor system plays an important role in cancer. SP promotes the proliferation of tumour cells, angiogenesis and the migration of tumour cells. We review the involvement of SP, the NK-1 receptor and NK-1 receptor antagonists in cancer. Tumour cells overexpress NK-1 receptors, which are involved in their viability. This overexpression suggests the possibility of specific treatment against tumour cells using NK-1 receptor antagonists, thus promoting a considerable decrease in the side effects of the treatment. This strategy opens up new approaches for cancer treatment, since these antagonists, after binding to their molecular target, induce the death of tumour cells by apoptosis, exert an antiangiogenic action and inhibit the migration of tumour cells. The use of NK-1 receptor antagonists such as aprepitant (used in clinical practice) as antitumour agents could be a promising innovation. The value of aprepitant as an antitumour agent could be determined faster than for less wellknown compounds because many studies addressing its safety and characterization have already been completed. The NK-1 receptor may be a promising target in the treatment of cancer; NK-1 receptor antagonists could act as specific drugs against tumour cells; and these antagonists could be new candidate anti-cancer drugs.

Indexed as

Angiogenesis InhibitorsAntineoplastic AgentsApoptosisAprepitantCell MovementCell ProliferationEmotionsHumansInflammationMorpholinesNeoplasmsNeovascularization, PathologicNeurokinin-1 Receptor AntagonistsReceptors, Neurokinin-1Substance PAngiogenesis InhibitorsAntineoplastic AgentsAprepitantMorpholinesNeurokinin-1 Receptor AntagonistsReceptors, Neurokinin-1Substance P

Identifiers

PMID25963269
OpenAlexW2000968765

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.