Evidence map›Paper›PMID 38327193›Full record

ArticleCancer discovery2024

Precision Targeting of Mutant PI3Kα.

Grace Q Gong, Bart Vanhaesebroeck

Abstract readComment
PubMed Publisher
In one paragraph

Article in Cancer discovery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. A renaissance in targeting the PI3K/AKT/mTOR pathway.Nature reviews. Drug discovery · 2026
    Review
  2. Article
  3. Article
  4. Making PI3K superfamily enzymes run faster.Advances in biological regulation · 2025
    Review
  5. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Grace Q GongUniversity College London Cancer Institute, University College London, London, United Kingdom.ORCID 0000-0002-7609-0466
Bart VanhaesebroeckUniversity College London Cancer Institute, University College London, London, United Kingdom.ORCID 0000-0002-7074-3673
London Cancer · GB

Funding

Cancer Research UK 25722Cancer Research UK 29269
6 · The paper itself

Abstract

PIK3CA, which encodes the p110α catalytic subunit of PI 3-kinase alpha (PI3Kα), is one of the most frequently genetically activated kinases in solid tumors. In two back-to-back papers, Varkaris and colleagues report on the development of a novel allosteric PI3Kα-mutant-selective inhibitor and early clinical experience with this compound. See related article by Varkaris et al., p. 227 (6) . See related article by Varkaris et al., p. 240 (5) .

Indexed as

Antineoplastic AgentsPhosphatidylinositol 3-KinasesClass I Phosphatidylinositol 3-KinasesHumansMutationPhosphoinositide-3 Kinase InhibitorsProtein Kinase InhibitorsAntineoplastic AgentsClass I Phosphatidylinositol 3-KinasesPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsProtein Kinase Inhibitors

Identifiers

PMID38327193
OpenAlexW4391657919

What Socratic 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 Socratic graph.