Evidence map›Paper›PMID 36969743›Full record

ArticleCancer research communications2022

Pharmaceutical Reactivation of Attenuated Apoptotic Pathways Leads to Elimination of Osimertinib Drug-Tolerant Cells.

Matthew J Martin, Nicolas Floc'h, Matthias Pfeifer, Steven Criscione, Oona Delpuech, Sladjana Gagrica, Yi Yao, Ultan McDermott, Paul D Smith

Open access · goldFull text read
In one paragraph

Article in Cancer research communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Drug-tolerant persister cancer cells.Journal of the National Cancer Center · 2024
    Article
  7. Review
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

9 authors at 2 institutions in 2 countries.

Matthew J MartinAstraZeneca Oncology R&D, Cambridge, United Kingdom.ORCID 0000-0002-8948-961X
Nicolas Floc'hAstraZeneca Oncology R&D, Cambridge, United Kingdom.
Matthias PfeiferAstraZeneca Oncology R&D, Cambridge, United Kingdom.ORCID 0000-0003-0065-9211
Steven CriscioneAstraZeneca Oncology R&D, Waltham, Boston, Massachusetts.
Oona DelpuechAstraZeneca Oncology R&D, Cambridge, United Kingdom.
Sladjana GagricaAstraZeneca Oncology R&D, Cambridge, United Kingdom.
Yi YaoAstraZeneca Oncology R&D, Waltham, Boston, Massachusetts.
Ultan McDermottAstraZeneca Oncology R&D, Cambridge, United Kingdom.
Paul D SmithAstraZeneca Oncology R&D, Cambridge, United Kingdom.ORCID 0000-0002-2812-5978
Abzena (United Kingdom) · GBBoston Engineering (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osimertinib is an EGFR tyrosine kinase inhibitor (TKI) with proven clinical efficacy; however, acquired resistance presents an obstacle to curing Significance: These studies uncover strategies to use targeted agents that activate apoptosis in non-small cell lung cancer cells that survive initial EGFR TKI treatment.

Indexed as

Antineoplastic AgentsCarcinoma, Non-Small-Cell LungLung NeoplasmsAcrylamidesAniline CompoundsAnimalsCell Line, TumorDrug Resistance, NeoplasmErbB ReceptorsHumansIndolesMicePharmaceutical PreparationsProtein Kinase InhibitorsPyrimidinesAcrylamidesAniline CompoundsAntineoplastic AgentsErbB ReceptorsIndolesosimertinibPharmaceutical PreparationsProtein Kinase InhibitorsPyrimidines

Identifiers

PMID36969743
PMCPMC10035388
OpenAlexW4295279596

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read46
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.