Evidence map›Paper›PMID 36376561›Full record

ReviewNature reviews. Drug discovery2023

Beyond PI3Ks: targeting phosphoinositide kinases in disease.

John E Burke, Joanna Triscott, Brooke M Emerling, Gerald R V Hammond

Open access · bronzeAbstract readReview
In one paragraph

Review in Nature reviews. Drug discovery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed
18.7field-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

96 citing papers in PubMed, 133 citations in OpenAlex.

  1. Review
  2. Review
  3. PI(3,5)PScience advances · 2026
    Article
  4. Quantitative comparison of PI(3,5)PMolecular biology of the cell · 2026
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36 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

4 authors at 4 institutions in 3 countries.

John E BurkeDepartment of Biochemistry and Microbiology, University of Victoria, Victoria, British Columbia, Canada. jeburke@uvic.ca.ORCID 0000-0001-7904-9859
Joanna TriscottDepartment of BioMedical Research, University of Bern, Bern, Switzerland.ORCID 0000-0002-0625-0524
Brooke M EmerlingSanford Burnham Prebys, La Jolla, CA, USA. bemerling@sbpdiscovery.org.ORCID 0000-0002-2168-4582
Gerald R V HammondDepartment of Cell Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA. ghammond@pitt.edu.ORCID 0000-0002-6660-3272
Sanford Burnham Prebys Medical Discovery Institute · USUniversity of Bern · CHUniversity of British Columbia · CAUniversity of Pittsburgh · US

Funding

WORK ORDER 126643 B539 EXPAND IC SUITE75N91019D00024 · NIAID · LEIDOS BIOMEDICAL RESEARCH, INC. · PI BRISCOE, LYNN · 2019 to 2025
$3932.6M
Directing Membrane Function with Inositol Lipids in Health and DiseaseR35GM119412 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Gerald R Hammond · 2016 to 2026
$4.3M
Function and Mechanism of the Hippo-PI5P4K Axis for Growth ControlR01GM143583 · NIGMS · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI EMERLING, BROOKE M. · 2022 to 2025
$2.2M
Non-Canonical Phosphatidylinositol Kinases in Triple Negative Breast CancerR01CA237536 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI EMERLING, BROOKE M · 2020 to 2024
$2.2M
PIP5K1A as a novel driver of PI3K signaling in health and diseaseR03TR003624 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HAMMOND, GERALD R · 2021 to 2021
$157k
NCATS NIH HHS R03 TR003624NCI NIH HHS 75N91019D00024NCI NIH HHS R01 CA237536NIGMS NIH HHS R01 GM143583NIGMS NIH HHS R35 GM119412
6 · The paper itself

Abstract

Lipid phosphoinositides are master regulators of almost all aspects of a cell's life and death and are generated by the tightly regulated activity of phosphoinositide kinases. Although extensive efforts have focused on drugging class I phosphoinositide 3-kinases (PI3Ks), recent years have revealed opportunities for targeting almost all phosphoinositide kinases in human diseases, including cancer, immunodeficiencies, viral infection and neurodegenerative disease. This has led to widespread efforts in the clinical development of potent and selective inhibitors of phosphoinositide kinases. This Review summarizes our current understanding of the molecular basis for the involvement of phosphoinositide kinases in disease and assesses the preclinical and clinical development of phosphoinositide kinase inhibitors.

Indexed as

NeoplasmsNeurodegenerative DiseasesVirus DiseasesHumansPhosphatidylinositol 3-KinasesPhosphatidylinositolsPhosphatidylinositol 3-KinasesPhosphatidylinositols

Identifiers

PMID36376561
PMCPMC9663198
OpenAlexW4308949853

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.