Evidence map›Paper›PMID 32019887›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Control of XPR1-dependent cellular phosphate efflux by InsP

Xingyao Li, Chunfang Gu, Sarah Hostachy, Soumyadip Sahu, Christopher Wittwer, Henning J Jessen, Dorothea Fiedler, Huanchen Wang, Stephen B Shears

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
9.3field-weighted citation impact, top 1% 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

79 citing papers in PubMed, 120 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

19 more citing papers are in PubMed but not listed here.

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 3 institutions in 2 countries.

Xingyao LiSignal Transduction Laboratory, National Institute of Environmental Health Sciences, NIH, Research Triangle Park, NC 27709.
Chunfang GuSignal Transduction Laboratory, National Institute of Environmental Health Sciences, NIH, Research Triangle Park, NC 27709.
Sarah HostachyChemical Biology Department, Leibniz-Forschungsinstitut für Molekulare Pharmakologie, 13125 Berlin, Germany.
Soumyadip SahuSignal Transduction Laboratory, National Institute of Environmental Health Sciences, NIH, Research Triangle Park, NC 27709.
Christopher WittwerInstitute of Organic Chemistry, University of Freiburg, 79104 Freiburg, Germany.ORCID 0000-0003-2393-0190
Henning J JessenInstitute of Organic Chemistry, University of Freiburg, 79104 Freiburg, Germany.ORCID 0000-0002-1025-9484
Dorothea FiedlerChemical Biology Department, Leibniz-Forschungsinstitut für Molekulare Pharmakologie, 13125 Berlin, Germany.
Huanchen WangSignal Transduction Laboratory, National Institute of Environmental Health Sciences, NIH, Research Triangle Park, NC 27709.ORCID 0000-0003-2701-7155
Stephen B ShearsSignal Transduction Laboratory, National Institute of Environmental Health Sciences, NIH, Research Triangle Park, NC 27709; shears@niehs.nih.gov.ORCID 0000-0001-7309-8916
National Institute of Environmental Health Sciences · USLeibniz-Forschungsinstitut für Molekulare Pharmakologie · DEUniversity of Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Homeostasis of cellular fluxes of inorganic phosphate (Pi) supervises its structural roles in bones and teeth, its pervasive regulation of cellular metabolism, and its functionalization of numerous organic compounds. Cellular Pi efflux is heavily reliant on Xenotropic and Polytropic Retrovirus Receptor 1 (XPR1), regulation of which is largely unknown. We demonstrate specificity of XPR1 regulation by a comparatively uncharacterized member of the inositol pyrophosphate (PP-InsP) signaling family: 1,5-bis-diphosphoinositol 2,3,4,6-tetrakisphosphate (InsP

Indexed as

Biological TransportHEK293 CellsHumansPhosphatesPhosphatidylinositol PhosphatesPhosphotransferases (Phosphate Group Acceptor)Receptors, G-Protein-CoupledReceptors, VirusSignal TransductionXenotropic and Polytropic Retrovirus Receptordiphosphoinositol pentakisphosphate kinaseinositol hexakisphosphate kinasePhosphatesPhosphatidylinositol PhosphatesPhosphotransferases (Phosphate Group Acceptor)Receptors, G-Protein-CoupledReceptors, VirusXenotropic and Polytropic Retrovirus ReceptorXPR1 protein, humaninositolmetabolismsignaling

Identifiers

PMID32019887
PMCPMC7035621
OpenAlexW3005030505

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.