Evidence map›Paper›PMID 35118422›Full record

ArticleNature cancer2021

The present and future of PI3K inhibitors for cancer therapy.

Pau Castel, Eneda Toska, Jeffrey A Engelman, Maurizio Scaltriti

Open access · greenAbstract read
In one paragraph

Article in Nature cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 123 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed, 3 pooled it
13.4field-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

123 citing papers in PubMed, 3 syntheses or guidelines pooled it, 213 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Thieno[3,2-International journal of molecular sciences · 2026
    Review
  11. Article
  12. Article
  13. Engineering selective PI3KActa pharmaceutica Sinica. B · 2026
    Article
  14. Review
  15. Article
  16. Article
  17. A renaissance in targeting the PI3K/AKT/mTOR pathway.Nature reviews. Drug discovery · 2026
    Review
  18. Article
  19. Article
  20. Clinicogenomic Landscape and Function ofJCO precision oncology · 2026
    Article

63 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 3 institutions in 2 countries.

Pau Castel *Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, CA, USA.ORCID http://orcid.org/0000-0002-4972-4347
Eneda Toska *Department of Oncology, Sidney Kimmel Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Jeffrey A EngelmanTreeline Biosciences, Watertown, MA, USA. jengelman@treelinebiosciences.com.
Maurizio ScaltritiEarly Oncology, AstraZeneca, Waltham, MA, USA. maurizio.scaltriti@astrazeneca.com.ORCID http://orcid.org/0000-0002-5522-1447
AstraZeneca (South Korea) · KRJohns Hopkins University · USUniversity of California, San Francisco · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
The role of Sin1 in Kras-driven cancerK99CA245122 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CASTEL, PAU · 2020 to 2021
$214k
NCI NIH HHS K99 CA245122NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Phosphoinositide-3- kinase (PI3K) signaling regulates cellular proliferation, survival and metabolism, and its aberrant activation is one of the most frequent oncogenic events across human cancers. In the last few decades, research focused on the development of PI3K inhibitors, from preclinical tool compounds to the highly specific medicines approved to treat patients with cancer. Herein we discuss current paradigms for PI3K inhibitors in cancer therapy, focusing on clinical data and mechanisms of action. We also discuss current limitations in the use of PI3K inhibitors including toxicities and mechanisms of resistance, with specific emphasis on approaches aimed to improve their efficacy.

Indexed as

NeoplasmsPhosphatidylinositol 3-KinasesHumansPhosphatidylinositol 3-KinasePhosphoinositide-3 Kinase InhibitorsSignal TransductionPhosphatidylinositol 3-KinasePhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase Inhibitors

Identifiers

PMID35118422
PMCPMC8809509
OpenAlexW3170740788

What OpenQuestion holds

Textmetadata
LicenceTDM
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.