Evidence map›Paper›PMID 35357905›Full record

ReviewJCO precision oncology2022

Aryana R Rasti, Amy Guimaraes-Young, Farrah Datko, Virginia F Borges, Dara L Aisner, Elena Shagisultanova

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in JCO precision oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07387861 (Immunohistochemical Evaluation of p-AKT and p-S6 as Surrogate Markers of PI3K/AKT/mTOR Pathway Activation in ER-Positive, HER2-Negative Breast Carcinoma), which is not on this map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
8.6field-weighted citation impact, top 2% 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.

NCT07387861 not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Immunohistochemical Evaluation of p-AKT and p-S6 as Surrogate Markers of PI3K/AKT/mTOR Pathway Activation in ER-Positive, HER2-Negative Breast Carcinoma

TypeobservationalSponsorAssiut UniversityRan2026 to 2028Enrolled70ConditionsBreast Cancer - ER+, HER2-, PIK3CA Gene MutationArmsNot applicable- observational study
3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Metabolic hallmarks of trastuzumab resistance.Expert opinion on therapeutic targets · 2025
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Case Report: FGFR2 inhibitor resistance viaFrontiers in oncology · 2025
    Article
  19. Observational
  20. 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

6 authors at 4 institutions in 1 country.

Aryana R RastiUniversity of Colorado School of Medicine, Aurora, CO.
Amy Guimaraes-YoungDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO.ORCID 0000-0002-8280-527X
Farrah DatkoUniversity of Colorado Health Cancer Center, Harmony Campus, Fort Collins, CO.
Virginia F BorgesYoung Women Breast Cancer Translational Program, University of Colorado Cancer Center, Aurora, CO.ORCID 0000-0003-1158-7524
Dara L AisnerDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO.ORCID 0000-0001-5203-5932
Elena ShagisultanovaYoung Women Breast Cancer Translational Program, University of Colorado Cancer Center, Aurora, CO.ORCID 0000-0003-1389-1116
University of Colorado Anschutz Medical Campus · USUniversity of Colorado Cancer Center · USUniversity of Colorado Denver · USUniversity of Colorado Health · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Discovering mechanisms of sensitivity and resistance to triple combination targeted therapy in HR+/HER2+ breast cancerK08CA241071 · NCI · UNIVERSITY OF COLORADO DENVER · PI SHAGISULTANOVA, ELENA · 2019 to 2023
$1.2M
NCI NIH HHS K08 CA241071NCI NIH HHS P30 CA046934
6 · The paper itself

Abstract

The phosphatidylinositol 3-kinase (PI3K) pathway is an intracellular pathway activated in response to progrowth signaling, such as human epidermal growth factor receptor 2 (HER2) and other kinases. Abnormal activation of PI3K has long been recognized as one of the main oncogenic drivers in breast cancer, including HER2-positive (HER2+) subtype. Somatic activating mutations in the gene encoding PI3K alpha catalytic subunit (

Indexed as

Breast NeoplasmsClass I Phosphatidylinositol 3-KinasesDrug Resistance, NeoplasmErb-b2 Receptor Tyrosine KinasesFemaleHumansMutationClass I Phosphatidylinositol 3-KinasesERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesPIK3CA protein, human

Identifiers

PMID35357905
PMCPMC8984255
OpenAlexW4220699574

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.