Evidence map›Paper›PMID 31492921›Full record

ArticleScientific reports2019

Phlda3 regulates beta cell survival during stress.

Mohammed Bensellam, Jeng Yie Chan, Kailun Lee, Mugdha V Joglekar, Anandwardhan A Hardikar, Thomas Loudovaris, Helen E Thomas, Jean-Christophe Jonas, D Ross Laybutt

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Inhibition ofBrain communications · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. PHLDA3 promotes lung adenocarcinoma cell proliferation and invasion via activation of the Wnt signaling pathway.Laboratory investigation; a journal of technical methods and pathology · 2021
    Article
  17. 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

9 authors at 5 institutions in 2 countries.

Mohammed BensellamGarvan Institute of Medical Research, Sydney, NSW, Australia. mohammed.bensellam@uclouvain.be.
Jeng Yie ChanGarvan Institute of Medical Research, Sydney, NSW, Australia.
Kailun LeeGarvan Institute of Medical Research, Sydney, NSW, Australia.
Mugdha V JoglekarNHMRC Clinical Trials Centre, The University of Sydney, Sydney, NSW, Australia.
Anandwardhan A HardikarNHMRC Clinical Trials Centre, The University of Sydney, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0001-5587-2090
Thomas LoudovarisSt. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.
Helen E ThomasSt. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.
Jean-Christophe JonasUniversité catholique de Louvain, Institut de recherche expérimentale et clinique, Pôle d'endocrinologie, diabète et nutrition, Brussels, Belgium.ORCID http://orcid.org/0000-0001-9882-5438
D Ross LaybuttGarvan Institute of Medical Research, Sydney, NSW, Australia. r.laybutt@garvan.org.au.
Garvan Institute of Medical Research · AUThe University of Sydney · AUSt Vincent's Hospital Melbourne · AUSt Vincents Institute of Medical Research · AUUCLouvain · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The loss of functional beta cell mass characterises all forms of diabetes. Beta cells are highly susceptible to stress, including cytokine, endoplasmic reticulum (ER) and oxidative stress. This study examined the role of pleckstrin homology-like, domain family A, member 3 (Phlda3) in beta cell survival under stress conditions and the regulatory basis. We found that the mRNA levels of Phlda3 were markedly upregulated in vivo in the islets of diabetic humans and mice. In vitro, exposure of MIN6 cells or islets to cytokines, palmitate, thapsigargin or ribose upregulated Phlda3 mRNA and protein levels, concurrent with the induction of ER stress (Ddit3 and Trb3) and antioxidant (Hmox1) genes. Furthermore, H

Indexed as

Stress, PhysiologicalAnimalsAntioxidantsCell DeathCell LineCell SurvivalCytokinesCytoprotectionEndoplasmic Reticulum Chaperone BiPEndoplasmic Reticulum StressFemaleHumansInsulin-Secreting CellsMice, Inbred C57BLMice, Inbred NODModels, BiologicalAntioxidantsCytokinesEndoplasmic Reticulum Chaperone BiPHSPA5 protein, humanHspa5 protein, mouseNF-kappa BNuclear ProteinsPalmitic AcidRNA, MessengerThapsigarginTSSC3 proteinX-Box Binding Protein 1

Identifiers

PMID31492921
PMCPMC6731300
OpenAlexW2971527258

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.