Evidence map›Paper›PMID 28360131›Full record

ArticleDevelopment (Cambridge, England)2017

A small-molecule screen reveals that HSP90β promotes the conversion of induced pluripotent stem cell-derived endoderm to a hepatic fate and regulates HNF4A turnover.

Ran Jing, Cameron B Duncan, Stephen A Duncan

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

21 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Organismal Roles of Hsp90.Biomolecules · 2023
    Review
  11. Review
  12. Review
  13. Article
  14. Protein quality control of cell stemness.Cell regeneration (London, England) · 2020
    Review
  15. Article
  16. Review
  17. Chaperones and Beyond as Key Players in Pluripotency Maintenance.Frontiers in cell and developmental biology · 2019
    Review
  18. Article
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Ran JingDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Basic Science Building BS657A, 173 Ashley Avenue, MSC 508, Charleston, SC 29425, USA.
Cameron B DuncanDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Basic Science Building BS657A, 173 Ashley Avenue, MSC 508, Charleston, SC 29425, USA.ORCID 0000-0002-2507-7827
Stephen A DuncanDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Basic Science Building BS657A, 173 Ashley Avenue, MSC 508, Charleston, SC 29425, USA duncanst@musc.edu.
Medical University of South Carolina · US

Funding

iPS-derived hepatocytes for interrogation of lipid phenotypesU01HG006398 · NHGRI · UNIVERSITY OF PENNSYLVANIA · PI RADER, DANIEL JAMES · 2011 to 2015
$8.6M
Molecular Basis of Human Hepatic Progenitor Cell FormationR01DK102716 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI DUNCAN, STEPHEN A · 2014 to 2022
$3.8M
Identification of Pathways Regulating Hepatocyte Differentiation from iPS CellsR21HD082570 · NICHD · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI DUNCAN, STEPHEN A · 2015 to 2016
$409k
MUTANT SCREENS FOR DEVELOPMENTALLY INTERACTING GENESF33HD008257 · NICHD · UNIVERSITY OF OREGON · PI EISEN, JUDITH S · 1997 to 1997
–
NHGRI NIH HHS U01 HG006398NICHD NIH HHS F33 HD008257NICHD NIH HHS R21 HD082570NIDDK NIH HHS R01 DK102716
6 · The paper itself

Abstract

We have previously shown that the transcription factor HNF4A is required for the formation of hepatic progenitor cells from endoderm that has been derived from human induced pluripotent stem cells (iPSCs). We reasoned that we could uncover regulatory pathways with new roles in hepatocyte differentiation by identifying cellular processes that regulate HNF4A. We therefore performed a screen of 1120 small molecules with well-characterized mechanisms of action to detect those that affect the abundance of HNF4A in iPSC-derived hepatic progenitor cells. This approach uncovered several small molecules that depleted HNF4A. Of those, we chose to focus on an inhibitor of heat shock protein 90 beta (HSP90β). We show that mutation of the gene encoding HSP90β represses hepatocyte differentiation during the formation of hepatocytes from iPSCs. We reveal that HSP90β, although dispensable for expression of

Indexed as

Cell DifferentiationHigh-Throughput Screening AssaysCells, CulturedEndodermHalf-LifeHepatocyte Nuclear Factor 4HepatocytesHSP90 Heat-Shock ProteinsHumansInduced Pluripotent Stem CellsLiverProtein DenaturationSmall Molecule LibrariesHepatocyte Nuclear Factor 4HNF4A protein, humanHSP90AB1 protein, humanHSP90 Heat-Shock ProteinsSmall Molecule LibrariesiPSC-derived hepatocytesLiver developmentSmall-molecule screening

Identifiers

PMID28360131
PMCPMC5450838
OpenAlexW2604093045

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.