Evidence map›Paper›PMID 14557546›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2003

Contrasting patterns of expression of transcription factors in pancreatic alpha and beta cells.

Jie Wang, Gene Webb, Yun Cao, Donald F Steiner

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Pancreatic beta cells lack a low glucose and O2-inducible mitochondrial protein that augments cell survival.Proceedings of the National Academy of Sciences of the United States of America · 2006
    Article
  11. Review
  12. 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

4 authors at 2 institutions in 1 country.

Jie WangDepartment of Biochemistry and Molecular Biology, University of Chicago, 5841 South Maryland Avenue, Chicago, IL 60637, USA.
Gene Webb
Yun Cao
Donald F Steiner
Howard Hughes Medical Institute · USUniversity of Chicago · US

Funding

TRANSGENIC COREP60DK020595 · NIDDK · UNIVERSITY OF CHICAGO · PI BELL, GRAEME I · 1985 to 2012
$25.5M
Pilot and Feasibility ProgramP30DK020595 · NIDDK · UNIVERSITY OF CHICAGO · PI Matthew J Brady · 2013 to 2026
$20.9M
STUDIES ON PANCREATIC HORMONESR01DK013914 · NIDDK · UNIVERSITY OF CHICAGO · PI STEINER, DONALD F · 1986 to 2011
$5.5M
STUDIES ON PANCREATIC HORMONESR37DK013914 · NIDDK · UNIVERSITY OF CHICAGO · PI STEINER, DONALD F · 1990 to 1997
–
NIDDK NIH HHS DK 13914NIDDK NIH HHS DK 20595NIDDK NIH HHS P30 DK020595NIDDK NIH HHS P60 DK020595NIDDK NIH HHS R01 DK013914
6 · The paper itself

Abstract

Pancreatic alpha and beta cells are derived from the same progenitors but play opposing roles in the control of glucose homeostasis. Disturbances in their function are associated with diabetes mellitus. To identify many of the proteins that define their unique pathways of differentiation and functional features, we have analyzed patterns of gene expression in alphaTC1.6 vs. MIN6 cell lines by using oligonucleotide microarrays. Approximately 9-10% of >11,000 transcripts examined showed significant differences between the two cell types. Of >700 known transcripts enriched in either cell type, transcription factors and their regulators (TFR) was one of the most significantly different categories. Ninety-six members of the basic zipper, basic helix-loop-helix, homeodomain, zinc finger, high mobility group, and other transcription factor families were enriched in alpha cells; in contrast, homeodomain proteins accounted for 51% of a total of 45 TFRs enriched in beta cells. Our analysis thus highlights fundamental differences in expression of TFR subtypes within these functionally distinct islet cell types. Interestingly, the alpha cells appear to express a large proportion of factors associated with progenitor or stem-type cells, perhaps reflecting their earlier appearance during pancreatic development. The implications of these findings for a better understanding of alpha and beta cell dysfunction in diabetes mellitus are also considered.

Indexed as

AnimalsCell LineCells, CulturedGene Expression RegulationIslets of LangerhansLeucine ZippersMiceMice, KnockoutReverse Transcriptase Polymerase Chain ReactionRNA, ComplementaryTranscription FactorsTranscription, GeneticZinc FingersRNA, ComplementaryTranscription Factors

Identifiers

PMID14557546
PMCPMC240674
OpenAlexW2104176411

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.