Evidence map›Paper›PMID 36046843›Full record

ReviewExploration of targeted anti-tumor therapy2022

Role of PI3K/Akt/mTOR pathway in mediating endocrine resistance: concept to clinic.

Aglaia Skolariki, Jamie D'Costa, Martin Little, Simon Lord

Registry-linked trialAbstract readReview
In one paragraph

Review in Exploration of targeted anti-tumor therapy, 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 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

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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.

Aglaia Skolariki *Department of Oncology, University of Oxford, Churchill Hospital, OX3 7LE Oxford, UK.ORCID https://orcid.org/0000-0001-5354-0359
Jamie D'Costa *Department of Oncology, University of Oxford, Churchill Hospital, OX3 7LE Oxford, UK.ORCID https://orcid.org/0000-0002-6644-0661
Martin LittleDepartment of Oncology, Churchill Hospital, OX3 7LE Oxford, UK.ORCID https://orcid.org/0000-0003-2592-1570
Simon LordDepartment of Oncology, University of Oxford, Churchill Hospital, OX3 7LE Oxford, UK.ORCID https://orcid.org/0000-0001-7946-5609

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The majority of breast cancers express the estrogen receptor (ER) and for this group of patients, endocrine therapy is the cornerstone of systemic treatment. However, drug resistance is common and a focus for breast cancer preclinical and clinical research. Over the past 2 decades, the PI3K/Akt/mTOR axis has emerged as an important driver of treatment failure, and inhibitors of mTOR and PI3K are now licensed for the treatment of women with advanced ER-positive breast cancer who have relapsed on first-line hormonal therapy. This review presents the preclinical and clinical data that led to this new treatment paradigm and discusses future directions.

Indexed as

Breast cancerendocrine therapyPI3K/Akt/mTOR pathway

Identifiers

PMID36046843
PMCPMC9400772

What Socratic holds

Textmetadata
LicenceCC BY
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.