Evidence map›Paper›PMID 35465359›Full record

ArticleiScience2022

Discovery of a novel SHIP1 agonist that promotes degradation of lipid-laden phagocytic cargo by microglia.

Chiara Pedicone, Sandra Fernandes, Alessandro Matera, Shea T Meyer, Stewart Loh, Jeung-Hoi Ha, Denzil Bernard, John D Chisholm, Rosa Chiara Paolicelli, William G Kerr

Open access · goldAbstract read
In one paragraph

Article in iScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. SHIP1 is required for T cell surveillance of occult malignancies.Cellular and molecular life sciences : CMLS · 2026
    Article
  2. Review
  3. Review
  4. Article
  5. SHIPi improves hematologic recovery after chemotherapy.Molecular medicine (Cambridge, Mass.) · 2025
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Genes · 2023
    Review
  17. Microglial INPP5D limits plaque formation and glial reactivity in the PSAPP mouse model of Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2023
    Article
  18. Pathological Roles of INPP5D in Alzheimer's Disease.Advances in experimental medicine and biology · 2023
    Article
  19. Molecules (Basel, Switzerland) · 2022
    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

10 authors at 4 institutions in 2 countries.

Chiara PediconeDepartment of Microbiology and Immunology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
Sandra FernandesDepartment of Microbiology and Immunology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
Alessandro MateraDepartment of Biomedical Sciences, University of Lausanne, Lausanne, Switzerland.
Shea T MeyerChemistry Department, Syracuse University, Syracuse, NY 13210, USA.
Stewart LohDepartment of Biochemistry & Molecular Biology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
Jeung-Hoi HaDepartment of Biochemistry & Molecular Biology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
Denzil BernardAtomwise, San Francisco, CA, USA.
John D ChisholmChemistry Department, Syracuse University, Syracuse, NY 13210, USA.
Rosa Chiara PaolicelliDepartment of Biomedical Sciences, University of Lausanne, Lausanne, Switzerland.
William G KerrDepartment of Microbiology and Immunology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
SUNY Upstate Medical University · USSyracuse University · USUniversity of Lausanne · CHHealthwise · US

Funding

Translating SHIP1 Genetics to Generate a Novel Alzheimers Pharmacologic AgentRF1AG059717 · NIA · UNIVERSITY OF KENTUCKY · PI ESTUS, STEVEN, HUMPHREY, MARY BETH · 2018 to 2019
$3.9M
NIA NIH HHS RF1 AG059717
6 · The paper itself

Abstract

Here, we describe the use of artificial intelligence to identify novel agonists of the SH2-containing 5' inositol phosphatase 1 (SHIP1). One of the compounds, K306, represents the most potent agonist identified to date. We find that K306 exhibits selectivity for SHIP1 vs. the paralog enzyme SHIP2, and this activation does not require the C2 domain of SHIP1 which other known SHIP1 agonists require. Thus, K306 represents a new class of SHIP1 agonists with a novel mode of agonism. Importantly, we find that K306 can suppress induction of inflammatory cytokines and iNOS in macrophages or microglia, but not by their SHIP1-deficient counterparts. K306 also reduces TNF-α production

Indexed as

Artificial intelligenceBiochemical mechanismBiochemistryCellular neuroscienceHealth sciences

Identifiers

PMID35465359
PMCPMC9020084
OpenAlexW4220918833

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.