Evidence map›Paper›PMID 28445593›Full record

ReviewJournal of surgical oncology2017

NR5A2 discovering compounds that block tumor growth in PDAC.

Robert Fletterick

Abstract readReview
In one paragraph

Review in Journal of surgical oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Clinical and Molecular Attributes and Evaluation of Pancreatic Cystic Neoplasm.Biochimica et biophysica acta. Reviews on cancer · 2023
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. 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

1 author at 1 institution in 1 country.

Robert FletterickDepartment of Biochemistry, School of Medicine, UCSF, San Francisco, California.ORCID http://orcid.org/0000-0003-4864-238X
University of California, San Francisco · US

Funding

Mechanisms of regulation of LRH-1, Nanog and SF-1 by DAX-1R01DK078075 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FLETTERICK, ROBERT J · 2008 to 2011
$1.5M
Nuclear receptor LRH-1 in pancreatic cancerR21CA140751 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FLETTERICK, ROBERT J · 2010 to 2011
$365k
NCI NIH HHS R21 CA140751NIDDK NIH HHS R01 DK078075
6 · The paper itself

Abstract

Pancreatic cancers depend on driver molecules, oncogene proteins such as RAS. NR5A2 protein is a transcription factor and either activates or inhibits transcription through actions at hundreds of enhancers. It has unusual properties with effects appearing in multiple signaling networks. NR5A2 is a pluripotency reprogramming factor in the class nuclear receptor. Its controlling hormone is PIP3. Experiments suggest NR5A2 activation drives PDAC and inhibitors blunt cancer cell proliferation.

Indexed as

Carcinoma, Pancreatic DuctalCell Transformation, NeoplasticHumansPancreatic NeoplasmsReceptors, Cytoplasmic and NuclearNR5A2 protein, humanReceptors, Cytoplasmic and NuclearLRH-1stem cellstructure-based inhibitor designβ-catenin

Identifiers

PMID28445593
PMCPMC5519325
OpenAlexW2608246637

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.