Evidence map›Paper›PMID 41218914›Full record

ReviewCancer reports (Hoboken, N.J.)2025

Nicotinic Acetylcholine Receptor Pathways in Cancer: From Psychiatric Clues to Therapeutic Opportunities.

Mohammad Hossein Azadi, Pouya Pazooki, Soheila Ajdary, Hamed Shafaroodi

Abstract readReview
In one paragraph

Review in Cancer reports (Hoboken, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
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.

Mohammad Hossein AzadiFaculty of Cellular and Molecular Sciences, College of Biological Sciences, Kharazmi University, Tehran, Iran.
Pouya PazookiFaculty of Cellular and Molecular Sciences, College of Biological Sciences, Kharazmi University, Tehran, Iran.ORCID 0000-0002-8609-5949
Soheila AjdaryDepartment of Immunology, Pasteur Institute of Iran, Tehran, Iran.
Hamed ShafaroodiPharmacology Department, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe prevalence of cancer poses significant challenges to treatment, largely because of drug resistance along with other side effects. Current studies have been investigating the growth factors more than other biologic tumor features, such as neurobiologic features. Here in this review, we highlight the role of nicotinic acetylcholine receptors (nAChRs) in cancer development with their context-dependent activation and downstream effectors. RECENT

findingsSome nAChR subtypes stimulate tumorigenic pathways, EGFR/ERK1/2, PI3K/AKT, and MAPK, with varying responses based on the receptor subtype and tissue type. Notably, the Src kinase and MAPK pathways are common downstream effectors in lung, breast, and prostate cancers despite the variations in the predominant nAChR subunits in each cancer: α7 in lung, α9 in breast, and likely α5 and α7 in prostate tumors.

conclusionThese findings underscore the importance of targeting nAChRs in a context-specific manner to modulate shared signaling pathways, particularly the acetylcholine-stimulated Src/MAPK pathway. This review also calls for more investigation on other neurotransmitters and potential common pathways, as implicated by psychological reports, to advance the understanding of cancer biology and therapies.

Indexed as

NeoplasmsReceptors, NicotinicAnimalsAntineoplastic AgentsHumansMolecular Targeted TherapySignal TransductionAntineoplastic AgentsReceptors, Nicotinicbreast cancerlung cancermolecular oncologynAChRsneurotransmittersprostate cancersignal transduction

Identifiers

PMID41218914
PMCPMC12616886

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Registered trials

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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.