Evidence map›Paper›PMID 33435517›Full record

ArticleInternational journal of molecular sciences2021

GPR55 Receptor Activation by the

Mikhail G Akimov, Alina M Gamisonia, Polina V Dudina, Natalia M Gretskaya, Anastasia A Gaydaryova, Andrey S Kuznetsov, Galina N Zinchenko, Vladimir V Bezuglov

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Targeting Oxidative Stress: Novel Coumarin-Based Inverse Agonists of GPR55.International journal of molecular sciences · 2021
    Article
  10. International journal of molecular sciences · 2021
    Article
  11. Cannabinoids in the landscape of cancer.Journal of cancer research and clinical oncology · 2021
    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

8 authors at 1 institution in 1 country.

Mikhail G AkimovShemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Ul. Miklukho-Maklaya, 16/10, Moscow 117997, Russia.ORCID 0000-0002-7467-4409
Alina M GamisoniaShemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Ul. Miklukho-Maklaya, 16/10, Moscow 117997, Russia.ORCID 0000-0001-8532-4714
Polina V DudinaShemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Ul. Miklukho-Maklaya, 16/10, Moscow 117997, Russia.
Natalia M GretskayaShemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Ul. Miklukho-Maklaya, 16/10, Moscow 117997, Russia.
Anastasia A GaydaryovaShemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Ul. Miklukho-Maklaya, 16/10, Moscow 117997, Russia.
Andrey S KuznetsovShemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Ul. Miklukho-Maklaya, 16/10, Moscow 117997, Russia.ORCID 0000-0001-7337-1441
Galina N ZinchenkoShemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Ul. Miklukho-Maklaya, 16/10, Moscow 117997, Russia.
Vladimir V BezuglovShemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Ul. Miklukho-Maklaya, 16/10, Moscow 117997, Russia.
Institute of Bioorganic Chemistry · RU

Funding

Russian Foundation for Basic Research 17-00-00105 KOMFIRussian Foundation for Basic Research 19-04-00302a
6 · The paper itself

Abstract

GPR55 is a GPCR of the non-CB1/CB2 cannabinoid receptor family, which is activated by lysophosphatidylinositol (LPI) and stimulates the proliferation of cancer cells. Anandamide, a bioactive lipid endocannabinoid, acts as a biased agonist of GPR55 and induces cancer cell death, but is unstable and psychoactive. We hypothesized that other endocannabinoids and structurally similar compounds, which are more hydrolytically stable, could also induce cancer cell death via GPR55 activation. We chemically synthesized and tested a set of fatty acid amides and esters for cell death induction via GPR55 activation. The most active compounds appeared to be

Indexed as

AnimalsAntineoplastic AgentsApoptosisCannabinoid Receptor AgonistsCell Line, TumorDopamineEnzyme ActivatorsFatty AcidsHumansMolecular Docking SimulationNeoplasmsNitric Oxide Synthase Type IPC12 CellsRatsReceptors, CannabinoidAntineoplastic AgentsCannabinoid Receptor AgonistsDopamineEnzyme ActivatorsFatty AcidsGPR55 protein, humanN-docosahexaenoyl dopamineNitric Oxide Synthase Type IReceptors, Cannabinoidcancer cell apoptosisendocannabinoidsGPR55N-acyldopaminesN-acyldopamines cytotoxicitynitric oxide synthase

Identifiers

PMID33435517
PMCPMC7826688
OpenAlexW3119386792

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.