Evidence map›Paper›PMID 2217207›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1990

Identification of three related human GRO genes encoding cytokine functions.

S Haskill, A Peace, J Morris, S A Sporn, A Anisowicz, S W Lee, T Smith, G Martin, P Ralph, R Sager

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1990. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed, 2 pooled it
7.2field-weighted citation impact, top 2% 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

86 citing papers in PubMed, 2 syntheses or guidelines pooled it, 289 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. circRNF13, a novel NCell death discovery · 2023
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. International journal of molecular sciences · 2022
    Review
  15. An Immune-Related Prognostic Risk Model in Colon Cancer by Bioinformatics Analysis.Evidence-based complementary and alternative medicine : eCAM · 2022
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Chemokines and Pain in the Trigeminal System.Frontiers in pain research (Lausanne, Switzerland) · 2021
    Review

26 more citing papers are in PubMed but not listed here.

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

10 authors at 1 institution in 1 country.

S HaskillDepartment of Obstetrics and Gynecology, Microbiology and Immunology, Lineberger Cancer Research Center, University of North Carolina, Chapel Hill 27599-7295.
A Peace
J Morris
S A Sporn
A Anisowicz
S W Lee
T Smith
G Martin
P Ralph
R Sager
University of North Carolina at Chapel Hill · US

Funding

ADHERENCE REGULATED MONOCYTE GENESR01AI026774 · NIAID · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI HASKILL, JOHN S · 1989 to 1999
–
GENOMIC CHANGES IN CANCER--MECHANISMS AND CONSEQUENCESR35CA039814 · NCI · DANA-FARBER CANCER INSTITUTE · PI SAGER, RUTH · 1985 to 1991
–
NCI NIH HHS CA39814NIAID NIH HHS AI26774
6 · The paper itself

Abstract

The product of the human GRO gene is a cytokine with inflammatory and growth-regulatory properties; GRO is also called MGSA for melanoma growth-stimulatory activity. We have identified two additional genes, GRO beta and GRO gamma, that share 90% and 86% identity at the deduced amino acid level with the original GRO alpha isolate. One amino acid substitution of proline in GRO alpha by leucine in GRO beta and GRO gamma leads to a large predicted change in protein conformation. Significant differences also exist in the 3' untranslated region, including different numbers of ATTTA repeats associated with mRNA instability. A 122-base-pair region in the 3' region is conserved among the three GRO genes, and a part of it is also conserved in the Chinese hamster genome, suggesting a role in regulation. DNA hybridization with oligonucleotide probes and partial sequence analysis of the genomic clones confirm that the three forms are derived from related but different genes. Only one chromosomal locus has been identified, at 4q21, by using a GRO alpha cDNA clone that hybridized to all three genes. Expression studies reveal tissue-specific regulation as well as regulation by specific inducing agents, including interleukin 1, tumor necrosis factor, phorbol 12-myristate 13-acetate, and lipopolysaccharide.

Indexed as

Chemokines, CXCIntercellular Signaling Peptides and ProteinsMultigene FamilyAmino Acid SequenceBase SequenceCells, CulturedChemokine CXCL1Chemokine CXCL2CytokinesDNAExonsGene LibraryGrowth SubstancesHumansInflammationIntronsChemokine CXCL1Chemokine CXCL2Chemokines, CXCCXCL1 protein, humanCXCL2 protein, humanCXCL3 protein, humanCytokinesDNAGrowth SubstancesIntercellular Signaling Peptides and Proteins

Identifiers

PMID2217207
PMCPMC54822
OpenAlexW1973195685

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.