Evidence map›Paper›PMID 21830214›Full record

ArticleJournal of cellular physiology2012

Functional role of an islet transcription factor, INSM1/IA-1, on pancreatic acinar cell trans-differentiation.

Tao Zhang, Nicolle A Saunee, Mary B Breslin, Kejing Song, Michael S Lan

Abstract read
In one paragraph

Article in Journal of cellular physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Function and Transcriptional Regulation of BovineInternational journal of molecular sciences · 2019
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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

5 authors at 2 institutions in 1 country.

Tao ZhangThe Research Institute for Children, Children's Hospital, New Orleans, Louisiana, USA.
Nicolle A Saunee
Mary B Breslin
Kejing Song
Michael S Lan
Children's Hospital of New Orleans · USLouisiana State University Health Sciences Center New Orleans · US

Funding

Transcription Factors in Neuroendocrine DifferentiationR01DK061436 · NIDDK · LOUISIANA STATE UNIV HSC NEW ORLEANS · PI LAN, MICHAEL S · 2003 to 2009
$1.5M
NIDDK NIH HHS DK61436NIDDK NIH HHS R01 DK061436
6 · The paper itself

Abstract

In this study, the functional role of INSM1 is examined with an AR42J acinar cell model for trans-differentiation into insulin-positive cells. Islet transcription factors (ITFs: INSM1, Pdx-1, and NeuroD1) are over-expressed in AR42J cells using adenoviral vectors. Addition of Ad-INSM1 alone or the combination of three ITFs to the AR42J cells triggers cellular trans-differentiation. Ectopic expression of INSM1 directly induces insulin, Pax6, and Nkx6.1 expression, whereas Pdx-1 and NeuroD1 were slightly suppressed by INSM1. Addition of Pdx-1 and NeuroD1 with INSM1 further enhances endocrine trans-differentiation by increasing both the numbers and intensity of the insulin-positive cells with simultaneous activation of ITFs, Ngn3 and MafA. INSM1 expression alone partially inhibits dexamethasone-induced exocrine amylase expression. The combination of the three ITFs completely inhibits amylase expression and concomitantly induces greater acinar cell trans-differentiation into endocrine cells. Also, addition of the three ITFs promotes EGF and TGFβ receptors expression. Stimulation by the three ITFs along with the EGF/TGFβ growth factors strongly promotes insulin gene expression. The combination of the three ITFs and EGF/TGFβ growth factors with the primary cultured pancreatic acini also facilitates exocrine to endocrine cell differentiation. Taken together, both the AR42J cell line and the primary cultured mouse acinar cells support INSM1 induced acini trans-differentiation model.

Indexed as

Cell TransdifferentiationAcinar CellsAdenoviridaeAmylasesAnimalsBasic Helix-Loop-Helix ProteinsCell Line, TumorCricetinaeDexamethasoneErbB ReceptorsEye ProteinsGenetic VectorsHomeodomain ProteinsInsulinIslets of LangerhansLectins, C-TypeAmylasesBasic Helix-Loop-Helix ProteinsDexamethasoneEgfr protein, ratErbB ReceptorsEye ProteinsHomeodomain ProteinsINSM1 protein, humanInsulinKlrg1 protein, ratLectins, C-TypeMembrane GlycoproteinsNerve Tissue ProteinsNeurog3 protein, ratNeurogenic differentiation factor 1Nkx6-1 protein, ratPaired Box Transcription Factorspancreatic and duodenal homeobox 1 proteinPAX6 protein, humanPax6 protein, mousePax6 protein, ratPAX6 Transcription FactorReceptors, Transforming Growth Factor betaRepressor ProteinsRNA, MessengerTrans-Activators

Identifiers

PMID21830214
PMCPMC3224187
OpenAlexW1977087101

What OpenQuestion holds

Textmetadata
LicenceTDM
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.