Evidence map›Paper›PMID 9125172›Full record

ArticleBiochemical and biophysical research communications1997

Adenosine A3 receptor agonists protect HL-60 and U-937 cells from apoptosis induced by A3 antagonists.

Y Yao, Y Sei, M P Abbracchio, J L Jiang, Y C Kim, K A Jacobson

Open access · greenAbstract read
In one paragraph

Article in Biochemical and biophysical research communications, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 105 citations in OpenAlex.

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  4. Involvement of AJournal of molecular neuroscience : MN · 2019
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  8. Adenosine receptors and cancer.Handbook of experimental pharmacology · 2009
    Review
  9. The Anti-Cancer Effect of AImmunology, endocrine & metabolic agents in medicinal chemistry · 2007
    Article
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  15. Article
  16. Article
  17. Article
  18. Article
  19. Adenosine A3 receptors: novel ligands and paradoxical effects.Trends in pharmacological sciences · 1998
    Review
  20. Article
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

6 authors at 2 institutions in 2 countries.

Y YaoLaboratory of Bioorganic Chemistry, NIDDK/NIH, Bethesda, Maryland 20892, USA.
Y Sei
M P Abbracchio
J L Jiang
Y C Kim
K A Jacobson
National Institutes of Health · USUniversity of Milan · IT

Funding

Drugs that Act at Adenosine ReceptorsZ01DK031117 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI JACOBSON, KENNETH ALAN · 1991 to 2008
$854k
Intramural NIH HHS Z01 DK031117Intramural NIH HHS Z99 DK999999
6 · The paper itself

Abstract

The effects of novel, selective adenosine (ADO) A3 receptor antagonists of diverse structure on cells of the human HL-60 leukemia and U-937 lymphoma cell lines were examined. Both 3-ethyl 5-benzyl 2-methyl-6-phenyl-4-phenylethynyl-1,4-(+/-)-dihydropyridine-3, 5-dicarboxylate (MRS 1191, 0.5 microM) and 6-carboxy-methyl-5, 9-dihydro-9-methyl-2-phenyl-[1,2,4]-triazolo [5,1-a][2,7]naphthyridine (L-249313, 0.5 microM) induced apoptotic cell death and expression of bak protein. Low concentrations of the A3 receptor agonist 2-chloro-N6-(3-iodobenzyl)adenosine-5'-N-methyluronamide (Cl-IB-MECA, 10 nM or 1 microM) protected against antagonist-induced cell death. At concentrations > or = 10 microM, the agonist alone produced apoptosis and bak expression in various cell lines. It is suggested that there exists a tonic low level of A3 receptor activation, possibly induced by release of endogenous adenosine, that results in cell protection.

Indexed as

Purinergic P1 Receptor AgonistsPurinergic P1 Receptor AntagonistsAdenosineApoptosisDihydropyridinesDNA FragmentationDose-Response Relationship, DrugHL-60 CellsHumansPyrazolesQuinazolinesTriazoles2-chloro-N(6)-(3-iodobenzyl)adenosine-5'-N-methyluronamide9-chloro-2-(2-furyl)-(1,2,4)triazolo(1,5-c)quinazolin-5-imineAdenosineAHC 52DihydropyridinesN(6)-(3-iodobenzyl)-5'-N-methylcarboxamidoadenosinePurinergic P1 Receptor AgonistsPurinergic P1 Receptor AntagonistsPyrazolesQuinazolinesTriazoles

Identifiers

PMID9125172
PMCPMC4309999
OpenAlexW1980447664

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.