Evidence map›Paper›PMID 36402737›Full record

ReviewAdvances in biological regulation2023

The mutational profiles and corresponding therapeutic implications of PI3K mutations in cancer.

Nathan K VanLandingham, Andrew Nazarenko, Jennifer R Grandis, Daniel E Johnson

Open access · greenAbstract readReview
In one paragraph

Review in Advances in biological regulation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

11 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Flavonoids extract fromWorld journal of experimental medicine · 2025
    Review
  4. Review
  5. Article
  6. Neddylation as a target in PIK3CA-mutated head and neck cancer.Biochemical and biophysical research communications · 2025
    Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. 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

4 authors at 2 institutions in 1 country.

Nathan K VanLandinghamDepartment of Otolaryngology - Head and Neck Surgery, University of California San Francisco, San Francisco, CA, USA.
Andrew NazarenkoNew York Medical College, Valhalla, NY, USA.
Jennifer R GrandisDepartment of Otolaryngology - Head and Neck Surgery, University of California San Francisco, San Francisco, CA, USA.
Daniel E JohnsonDepartment of Otolaryngology - Head and Neck Surgery, University of California San Francisco, San Francisco, CA, USA. Electronic address: Daniel.Johnson@ucsf.edu.
University of California, San Francisco · USNew York Medical College · US

Funding

Integrating genomics and the protein interactome for HPV+ head and neck cancer therapyR35CA231998 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GRANDIS, JENNIFER RUBIN · 2018 to 2024
$6.2M
PI3K Pathway Mutations in Head and Neck CancerR01DE023685 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GRANDIS, JENNIFER RUBIN, JOHNSON, DANIEL E · 2014 to 2023
$5.1M
Targeting STAT3 to enhance anti-tumor immunityR01DE028289 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GRANDIS, JENNIFER RUBIN, JOHNSON, DANIEL E · 2019 to 2023
$3.2M
NCI NIH HHS R35 CA231998NIDCR NIH HHS R01 DE023685NIDCR NIH HHS R01 DE028289
6 · The paper itself

Abstract

Genetic alterations of the PIK3CA gene, encoding the p110α catalytic subunit of PI3Kα enzyme, are found in a broad spectrum of human cancers. Many cancer-associated PIK3CA mutations occur at 3 hotspot locations and are termed canonical mutations. Canonical mutations result in hyperactivation of PI3K and promote oncogenesis via the PI3K/AKT/mTOR and PI3K/COX-2/PGE2 signaling pathways. These mutations also may serve as predictive biomarkers of response to PI3K inhibitors, as well as NSAID therapy. A large number of non-canonical PIK3CA mutations have also been identified in human tumors, but their functional properties are poorly understood. Here we review the landscape of PIK3CA mutations in different cancers and efforts underway to define the functional properties of non-canonical PIK3CA mutations. In addition, we summarize what has been learned from clinical trials of PI3K inhibitors as well as current trials incorporating these molecular targeting agents.

Indexed as

NeoplasmsPhosphatidylinositol 3-KinasesClass I Phosphatidylinositol 3-KinasesHumansMutationPhosphoinositide-3 Kinase InhibitorsSignal TransductionClass I Phosphatidylinositol 3-KinasesPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsAlpelisibp110alphaPhosphoinositide 3-kinase alphaPIK3CA

Identifiers

PMID36402737
PMCPMC9992323
OpenAlexW4309338926

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.